Variant #0000261858 (NC_000017.10:g.79477716T>C, NM_001077182.2:c.-17842T>C (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.79477716T>C
DNA change (hg38) g.81510690T>C
Published as ACTG1(NM_001199954.2):c.1128A>G (p.*376=)
ISCN -
DB-ID ACTG1_000024
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) 0.02218 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-14 15:47:39 +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.-17842T>C r.(?) p.(=)
ACTG1 NM_001614.3 -/. - c.1128A>G r.(?) p.(Ter376=)


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