Variant #0000333971 (NC_000023.10:g.48123311dup, NM_005635.2:c.425dup (SSX1))

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.48123311dup
DNA change (hg38) g.48263876dup
Published as SSX1(NM_001278691.1):c.419_420insC (p.(Gly143ArgfsTer7)), SSX1(NM_001278691.1):c.425dupC (p.G143Rfs*7), SSX1(NM_005635.4):c.425dupC (p.G143Rfs*7)
ISCN -
DB-ID SSX1_000049 See all 3 reported entries
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
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SSX1 NM_005635.2 ?/. - c.425dup r.(?) p.(Gly143ArgfsTer7)


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