Variant #0000333208 (NC_000023.10:g.13797964_13797966del, GPM6B(NM_001001995.1):c.670_672del)

Chromosome X
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.13797964_13797966del
DNA change (hg38) g.13779845_13779847del
Published as GPM6B(NM_001001994.1):c.493_495del (p.(Gln165del))
ISCN -
DB-ID GPM6B_000010
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPM6B NM_001001995.1 ?/. - c.670_672del r.(?) p.(Gln224del)