Variant #0000610263 (NC_000006.11:g.31721147dup, NM_002441.4:c.882dup (MSH5))

Chromosome 6
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.31721147dup
DNA change (hg38) g.31753370dup
Published as MSH5(NM_002441.4):c.876_877insT (p.(Leu295SerfsTer75))
ISCN -
DB-ID MSH5_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) 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH5 NM_002441.4 ?/. - c.882dup r.(?) p.(Leu295SerfsTer75)
MSH5-SAPCD1 NR_037846.1 ?/. - n.1061dup r.(?) -


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