Variant #0000559236 (NC_000016.9:g.79633085C>T, MAF(NM_001031804.2):c.715G>A)

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.79633085C>T
DNA change (hg38) g.79599188C>T
Published as MAF(NM_001031804.2):c.715G>A (p.A239T)
ISCN -
DB-ID MAF_000028
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) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAF NM_001031804.2 -/. - c.715G>A r.(?) p.(Ala239Thr)
MAF NM_005360.4 -/. - c.715G>A r.(?) p.(Ala239Thr)