Variant #0000128806 (NC_000016.9:g.1840994C>T, IGFALS(NM_004970.2):c.1425G>A)

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.1840994C>T
DNA change (hg38) g.1790993C>T
Published as -
ISCN -
DB-ID IGFALS_000019 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs9282729
Origin Germline
Segregation -
Frequency 0-0.02
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00464 View details
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.1425G>A r.(?) p.(=)