Variant #0000692518 (NC_000017.10:g.79477848G>T, NM_001077182.2:c.-17710G>T (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.79477848G>T
DNA change (hg38) -
Published as ACTG1(NM_001199954.2):c.996C>A (p.P332=)
ISCN -
DB-ID ACTG1_000116 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) 0.00012 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.-17710G>T r.(?) p.(=)
ACTG1 NM_001614.3 -?/. - c.996C>A r.(?) p.(Pro332=)


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