Variant #0001007028 (NC_000017.10:g.79478243G>A, NM_001614.3:c.773C>T (ACTG1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.79478243G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ACTG1_000022 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs11549191
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-08-28 16:47:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACTG1 NM_001614.3 +?/. - c.773C>T r.(?) p.(Pro258Leu)


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