Variant #0000692519 (NC_000017.10:g.79478120C>T, NM_001077182.2:c.-17438C>T (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.79478120C>T
DNA change (hg38) -
Published as ACTG1(NM_001199954.2):c.817G>A (p.G273S)
ISCN -
DB-ID ACTG1_000138
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) 0 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
FSCN2 NM_001077182.2 ?/. - c.-17438C>T r.(?) p.(=)
ACTG1 NM_001614.3 ?/. - c.817G>A r.(?) p.(Gly273Ser)


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