Variant #0000995180 (NC_000005.9:g.79950737dup, NM_002439.4:c.191dup (MSH3))

Chromosome 5
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.79950737dup
DNA change (hg38) -
Published as MSH3(NM_002439.4):c.191dup (p.(Ala65SerfsTer20))
ISCN -
DB-ID DHFR_000102
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 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     
DHFR NM_000791.3 ?/. - c.-425dup r.(?) p.(=)
MTRNR2L2 NM_001190470.1 ?/. - c.-4828dup r.(?) p.(=)
MSH3 NM_002439.4 ?/. - c.191dup r.(?) p.(Ala65Serfs*20)


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