Version: 8.0.0
Date: Tue Jan 28 2025
15 results
Allele/Variant Genes: ARRDC3 (Hsa)

(GRCh38)5:91374955G>A

(Homo sapiens)
Allele/Variant
Source: rs1582371030
Genes: ARRDC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:91374955G>A

(GRCh38)5:91375516G>T

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.91375516G>T
Genes: ARRDC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:91375516G>T

(GRCh38)5:91375055A>G

(Homo sapiens)
Allele/Variant
Source: rs373902781
Genes: ARRDC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:91375055A>G

(GRCh38)5:91371404C>T

(Homo sapiens)
Allele/Variant
Source: rs769484237
Genes: ARRDC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:91371404C>T

(GRCh38)5:91371456T>C

(Homo sapiens)
Allele/Variant
Source: rs763354083
Genes: ARRDC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:91371456T>C

(GRCh38)5:91374125T>C

(Homo sapiens)
Allele/Variant
Source: rs386352279
Genes: ARRDC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:91374125T>C

(GRCh38)5:91376727C>T

(Homo sapiens)
Allele/Variant
Source: rs377260429
Genes: ARRDC3 (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)5:91376727C>T

(GRCh38)5:91383023A>G

(Homo sapiens)
Allele/Variant
Source: rs780018247
Genes: ARRDC3 (Hsa), ARRDC3-AS1 (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)5:91383023A>G

(GRCh38)5:91371444G>C

(Homo sapiens)
Allele/Variant
Source: rs765625079
Genes: ARRDC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:91371444G>C

(GRCh38)5:91375564G>A

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.91375564G>A
Genes: ARRDC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:91375564G>A

(GRCh38)5:91376678T>C

(Homo sapiens)
Allele/Variant
Source: rs34152201
Genes: ARRDC3 (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)5:91376678T>C

(GRCh38)5:91376698G>A

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.91376698G>A
Genes: ARRDC3 (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)5:91376698G>A

(GRCh38)5:91375113C>T

(Homo sapiens)
Allele/Variant
Source: rs746286312
Genes: ARRDC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:91375113C>T

(GRCh38)5:91373835G>A

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.91373835G>A
Genes: ARRDC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:91373835G>A

(GRCh38)5:91378745G>A

(Homo sapiens)
Allele/Variant
Source: rs147788981
Genes: ARRDC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:91378745G>A