Variant #0000573886 (NC_000023.10:g.13797938G>A, GPM6B(NM_001001995.1):c.696C>T)

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.13797938G>A
DNA change (hg38) g.13779819G>A
Published as GPM6B(NM_001001994.1):c.519C>T (p.(=))
ISCN -
DB-ID GPM6B_000014
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) 0.00185 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPM6B NM_001001995.1 -?/. - c.696C>T r.(?) p.(Tyr232=)