Version: 8.0.0
Date: Tue Jan 28 2025
25 results for apr3

ATRAID

(Homo sapiens)
Gene
Name: all-trans retinoic acid induced differentiation factor
Synonyms: APR-3, apoptosis related protein 3, p18, apoptosis related protein APR-3, APR--3, PRO240, all-trans retinoic acid-induced differentiation factor, HSPC013, APR3, apoptosis-related protein 3, C2orf28
Source: HGNC:24090
Biotype: protein coding gene
Synonyms: APR3...APR3

(GRCh38)2:27215521G>A

(Homo sapiens)
Allele/Variant
Source: rs774832372
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215521G>A
Gene Synonyms: APR3

(GRCh38)2:27215699G>T

(Homo sapiens)
Allele/Variant
Source: rs571082250
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215699G>T
Gene Synonyms: APR3

(GRCh38)2:27212325C>G

(Homo sapiens)
Allele/Variant
Source: rs1274336481
Genes: ATRAID (Hsa), SLC5A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27212325C>G
Gene Synonyms: APR3

(GRCh38)2:27215648G>C

(Homo sapiens)
Allele/Variant
Source: rs776772424
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215648G>C
Gene Synonyms: APR3

(GRCh38)2:27216937A>G

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.27216937A>G
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27216937A>G
Gene Synonyms: APR3

(GRCh38)2:27212295G>C

(Homo sapiens)
Allele/Variant
Source: rs762557057
Genes: ATRAID (Hsa), SLC5A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27212295G>C
Gene Synonyms: APR3

(GRCh38)2:27212381G>T

(Homo sapiens)
Allele/Variant
Source: rs773247722
Genes: ATRAID (Hsa), SLC5A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27212381G>T
Gene Synonyms: APR3

(GRCh38)2:27212447A>G

(Homo sapiens)
Allele/Variant
Source: rs1674616852
Genes: ATRAID (Hsa), SLC5A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27212447A>G
Gene Synonyms: APR3

(GRCh38)2:27216598A>T

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.27216598A>T
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27216598A>T
Gene Synonyms: APR3

(GRCh38)2:27213202T>C

(Homo sapiens)
Allele/Variant
Source: rs201877637
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27213202T>C
Gene Synonyms: APR3

(GRCh38)2:27213222G>C

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.27213222G>C
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27213222G>C
Gene Synonyms: APR3

(GRCh38)2:27216546T>C

(Homo sapiens)
Allele/Variant
Source: rs201778106
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27216546T>C
Gene Synonyms: APR3

(GRCh38)2:27215724A>G

(Homo sapiens)
Allele/Variant
Source: rs779575892
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215724A>G
Gene Synonyms: APR3

(GRCh38)2:27212345A>T

(Homo sapiens)
Allele/Variant
Source: rs369544433
Genes: ATRAID (Hsa), SLC5A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27212345A>T
Gene Synonyms: APR3

(GRCh38)2:27212298G>A

(Homo sapiens)
Allele/Variant
Source: rs765299018
Genes: ATRAID (Hsa), SLC5A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27212298G>A
Gene Synonyms: APR3

(GRCh38)2:27212393C>T

(Homo sapiens)
Allele/Variant
Source: rs185160026
Genes: ATRAID (Hsa), SLC5A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27212393C>T
Gene Synonyms: APR3

(GRCh38)2:27215520C>T

(Homo sapiens)
Allele/Variant
Source: rs147821107
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215520C>T
Gene Synonyms: APR3

(GRCh38)2:27212465G>A

(Homo sapiens)
Allele/Variant
Source: rs866330510
Genes: ATRAID (Hsa), SLC5A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27212465G>A
Gene Synonyms: APR3

(GRCh38)2:27215735A>G

(Homo sapiens)
Allele/Variant
Source: rs369720973
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215735A>G
Gene Synonyms: APR3

(GRCh38)2:27215742C>G

(Homo sapiens)
Allele/Variant
Source: rs748140857
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215742C>G
Gene Synonyms: APR3

(GRCh38)2:27216929G>A

(Homo sapiens)
Allele/Variant
Source: rs148460328
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27216929G>A
Gene Synonyms: APR3

(GRCh38)2:27212331C>T

(Homo sapiens)
Allele/Variant
Source: rs559815627
Genes: ATRAID (Hsa), SLC5A6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27212331C>T
Gene Synonyms: APR3

(GRCh38)2:27216904A>T

(Homo sapiens)
Allele/Variant
Source: rs1674869385
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27216904A>T
Gene Synonyms: APR3

(GRCh38)2:27215499G>A

(Homo sapiens)
Allele/Variant
Source: rs147492156
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215499G>A
Gene Synonyms: APR3