Version: 8.0.0
Date: Tue Jan 28 2025
4 results
Allele/Variant Genes: ARRDC3 (Hsa) Molecular Consequence: intron variant

(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)5:91376678T>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