Variant #0000325765 (NC_000017.10:g.79479055C>A, NM_001077182.2:c.-16503C>A (FSCN2))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.79479055C>A
DNA change (hg38) g.81512029C>A
Published as ACTG1(NM_001199954.1):c.237G>T (p.(Trp79Cys))
ISCN -
DB-ID ACTG1_000055
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FSCN2 NM_001077182.2 ?/. - c.-16503C>A r.(?) p.(=)
ACTG1 NM_001614.3 ?/. - c.237G>T r.(?) p.(Trp79Cys)


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