Variant #0000259929 (NC_000017.10:g.79478295C>G, NM_001077182.2:c.-17263C>G (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.79478295C>G
DNA change (hg38) g.81511269C>G
Published as ACTG1(NM_001199954.2):c.721G>C (p.E241Q)
ISCN -
DB-ID ACTG1_000038 See all 2 reported entries
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FSCN2 NM_001077182.2 ?/. - c.-17263C>G r.(?) p.(=)
ACTG1 NM_001614.3 ?/. - c.721G>C r.(?) p.(Glu241Gln)


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