Variant #0000642079 (NC_000017.10:g.79479026G>A, NM_001614.3:c.266C>T (ACTG1))

Chromosome 17
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.79479026G>A
DNA change (hg38) g.81512000G>A
Published as -
ISCN -
DB-ID ACTG1_000007 See all 3 reported entries
Variant remarks -
Reference MORL Deafness Variation Database, PubMed: Shearer 1993, PubMed: Zhu 2003, PubMed: Bryan 2009
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Global Variome, with Curator vacancy
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2020-02-05 13:36:16 +01:00 (CET)
Date last edited 2020-04-16 16:06:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACTG1 NM_001614.3 +/+ 3 c.266C>T r.(?) p.(Thr89Ile)


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