Variant #0001056236 (NC_000017.10:g.79479252A>C, NM_001077182.2:c.-16306A>C (FSCN2))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.79479252A>C
DNA change (hg38) -
Published as ACTG1(NM_001614.5):c.123+6T>G
ISCN -
DB-ID ACTG1_000155
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
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.-16306A>C r.(?) p.(=)
ACTG1 NM_001614.3 -?/. - c.123+6T>G r.(=) p.(=)


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