Variant #0001006830 (NC_000023.10:g.49173750T>A, NM_001098413.2:c.311T>A (GAGE10))

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.49173750T>A
DNA change (hg38) -
Published as GAGE10(NM_001098413.2):c.311T>A (p.(Val104Glu))
ISCN -
DB-ID GAGE10_000006
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) 1.0E-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
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GAGE12J NM_001098406.1 ?/. - c.-4882T>A r.(?) p.(=)
GAGE10 NM_001098413.2 ?/. - c.311T>A r.(?) p.(Val104Glu)


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