Variant #0000728997 (NC_000023.10:g.49218392C>T, NM_001477.1:c.157C>T (GAGE12I))

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.49218392C>T
DNA change (hg38) -
Published as GAGE12I(NM_001477.1):c.157C>T (p.P53S), GAGE4(NM_001474.1):c.157C>T (p.P53S), GAGE5(NM_001475.1):c.157C>T (p.P53S)
ISCN -
DB-ID GAGE2D_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GAGE2D NM_001098407.1 ?/. - c.*4066C>T r.(=) p.(=)
GAGE12I NM_001477.1 ?/. - c.157C>T r.(?) p.(Pro53Ser)


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