Variant #0000334181 (NC_000023.10:g.51486964C>A, GSPT2(NM_018094.4):c.242C>A)

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.51486964C>A
DNA change (hg38) g.51743868C>A
Published as GSPT2(NM_018094.4):c.242C>A (p.(Thr81Asn))
ISCN -
DB-ID GSPT2_000008
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) 2.0E-5 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     
GSPT2 NM_018094.4 ?/. - c.242C>A r.(?) p.(Thr81Asn)