Variant #0000726766 (NC_000017.10:g.79478469G>A, NM_001077182.2:c.-17089G>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.79478469G>A
DNA change (hg38) -
Published as ACTG1(NM_001199954.2):c.547C>T (p.R183W)
ISCN -
DB-ID ACTG1_000140
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FSCN2 NM_001077182.2 ?/. - c.-17089G>A r.(?) p.(=)
ACTG1 NM_001614.3 ?/. - c.547C>T r.(?) p.(Arg183Trp)


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