Version: 8.1.0
Date: Fri Apr 18 2025
139 results for ADNP-AS1

ADNP-AS1

(Homo sapiens)
Gene
Name: ADNP antisense RNA 1
Synonyms: Not Available
Source: HGNC:51227
Biotype: ncRNA gene
Symbol: ADNP-AS1 (Hsa)
Symbol: ADNP-AS1

(GRCh38)20:50945916T>C

(Homo sapiens)
Allele/Variant
Source: rs139211110
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945916T>C

(GRCh38)20:50945933A>G

(Homo sapiens)
Allele/Variant
Source: rs765027931
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945933A>G

(GRCh38)20:50945972A>G

(Homo sapiens)
Allele/Variant
Source: rs144979487
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945972A>G

(GRCh38)20:50945874A>G

(Homo sapiens)
Allele/Variant
Source: rs1210335567
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945874A>G

(GRCh38)20:50945880G>A

(Homo sapiens)
Allele/Variant
Source: rs749555898
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945880G>A

(GRCh38)20:50945916T>A

(Homo sapiens)
Allele/Variant
Source: rs139211110
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945916T>A

(GRCh38)20:50945724A>G

(Homo sapiens)
Allele/Variant
Source: rs201703497
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945724A>G

(GRCh38)20:50935248A>C

(Homo sapiens)
Allele/Variant
Source: rs1985048219
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50935248A>C

(GRCh38)20:50936206T>C

(Homo sapiens)
Allele/Variant
Source: rs1036628226
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50936206T>C

(GRCh38)20:50936209C>A

(Homo sapiens)
Allele/Variant
Source: rs760063295
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50936209C>A

(GRCh38)20:50945738T>G

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.50945738T>G
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945738T>G

(GRCh38)20:50945773A>G

(Homo sapiens)
Allele/Variant
Source: rs750138754
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945773A>G

(GRCh38)20:50945937T>G

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.50945937T>G
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945937T>G

(GRCh38)20:50945932G>C

(Homo sapiens)
Allele/Variant
Source: rs1986258505
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945932G>C

(GRCh38)20:50945935A>G

(Homo sapiens)
Allele/Variant
Source: rs200030885
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945935A>G

(GRCh38)20:50945750G>A

(Homo sapiens)
Allele/Variant
Source: rs752831768
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945750G>A

(GRCh38)20:50936142G>T

(Homo sapiens)
Allele/Variant
Source: rs186831786
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50936142G>T

(GRCh38)20:50935248A>T

(Homo sapiens)
Allele/Variant
Source: rs1985048219
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50935248A>T

(GRCh38)20:50940932G>A

(Homo sapiens)
Allele/Variant
Source: rs547949792
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50940932G>A

(GRCh38)20:50942077C>T

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.50942077C>T
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50942077C>T

(GRCh38)20:50945717A>G

(Homo sapiens)
Allele/Variant
Source: rs199721166
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945717A>G

(GRCh38)20:50945893G>A

(Homo sapiens)
Allele/Variant
Source: rs1986256273
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945893G>A

(GRCh38)20:50945932G>T

(Homo sapiens)
Allele/Variant
Source: rs1986258505
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945932G>T

(GRCh38)20:50935243T>A

(Homo sapiens)
Allele/Variant
Source: rs60224379
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50935243T>A

(GRCh38)20:50936147C>G

(Homo sapiens)
Allele/Variant
Source: rs1985138848
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50936147C>G

(GRCh38)20:50940850A>G

(Homo sapiens)
Allele/Variant
Source: rs1285003493
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50940850A>G

(GRCh38)20:50942096G>A

(Homo sapiens)
Allele/Variant
Source: rs755070736
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50942096G>A

(GRCh38)20:50934941T>C

(Homo sapiens)
Allele/Variant
Source: rs771510447
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50934941T>C

(GRCh38)20:50935120A>G

(Homo sapiens)
Allele/Variant
Source: rs758875594
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50935120A>G

(GRCh38)20:50942119T>C

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.50942119T>C
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50942119T>C

(GRCh38)20:50945751A>G

(Homo sapiens)
Allele/Variant
Source: rs1555822595
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945751A>G

(GRCh38)20:50945753T>C

(Homo sapiens)
Allele/Variant
Source: rs1986245938
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945753T>C

(GRCh38)20:50945835C>T

(Homo sapiens)
Allele/Variant
Source: rs1986251321
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945835C>T

(GRCh38)20:50945928A>G

(Homo sapiens)
Allele/Variant
Source: rs1986258168
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945928A>G

(GRCh38)20:50945862A>G

(Homo sapiens)
Allele/Variant
Source: rs371895653
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945862A>G

(GRCh38)20:50945882A>T

(Homo sapiens)
Allele/Variant
Source: rs2123115865
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945882A>T

(GRCh38)20:50945861C>G

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.50945861C>G
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945861C>G

(GRCh38)20:50946172A>T

(Homo sapiens)
Allele/Variant
Source: rs6126129
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50946172A>T

(GRCh38)20:50945851T>C

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.50945851T>C
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50945851T>C

(GRCh38)20:50936259T>C

(Homo sapiens)
Allele/Variant
Source: rs897083759
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50936259T>C

(GRCh38)20:50942048C>A

(Homo sapiens)
Allele/Variant
Source: rs1470781231
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50942048C>A

(GRCh38)20:50942051A>T

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.50942051A>T
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50942051A>T

(GRCh38)20:50935102T>C

(Homo sapiens)
Allele/Variant
Source: rs138782582
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50935102T>C

(GRCh38)20:50936140T>C

(Homo sapiens)
Allele/Variant
Source: rs771147863
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50936140T>C

(GRCh38)20:50936180G>A

(Homo sapiens)
Allele/Variant
Source: rs772868408
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50936180G>A

(GRCh38)20:50936192C>G

(Homo sapiens)
Allele/Variant
Source: rs765866526
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50936192C>G

(GRCh38)20:50936282T>C

(Homo sapiens)
Allele/Variant
Source: rs201186989
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50936282T>C

(GRCh38)20:50936367A>G

(Homo sapiens)
Allele/Variant
Source: rs2294902
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50936367A>G

(GRCh38)20:50941128C>G

(Homo sapiens)
Allele/Variant
Source: rs185402578
Genes: ADNP-AS1 (Hsa), DPM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:50941128C>G