Variant #0000563671 (NC_000017.10:g.79478236C>T, NM_001077182.2:c.-17322C>T (FSCN2))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.79478236C>T
DNA change (hg38) g.81511210C>T
Published as ACTG1(NM_001199954.2):c.780G>A (p.A260=)
ISCN -
DB-ID ACTG1_000090
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) 0.00305 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-14 15:50:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FSCN2 NM_001077182.2 -/. - c.-17322C>T r.(?) p.(=)
ACTG1 NM_001614.3 -/. - c.780G>A r.(?) p.(Ala260=)


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