Variant #0000128816 (NC_000016.9:g.1841480C>A, IGFALS(NM_004970.2):c.939G>T)

Chromosome 16
Allele Parent #1
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.1841480C>A
DNA change (hg38) g.1791479C>A
Published as -
ISCN -
DB-ID IGFALS_000022
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs35078715
Origin Germline
Segregation -
Frequency 0-0.01
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGFALS NM_004970.2 ?/. 2 c.939G>T r.(?) p.(=)