Variant #0000878334 (NC_000016.9:g.1841467C>G, IGFALS(NM_004970.2):c.952G>C)

Chromosome 16
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.1841467C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID IGFALS_000042
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs897198501
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGFALS NM_004970.2 ?/. - c.952G>C r.(?) p.(Glu318Gln)