Variant #0000526165 (NC_000005.9:g.80024689dup, NM_002439.4:c.1473dup (MSH3))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.80024689dup
DNA change (hg38) g.80728870dup
Published as MSH3(NM_002439.4):c.1473dupC (p.I492Hfs*3)
ISCN -
DB-ID DHFR_000039
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-17 11:44:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHFR NM_000791.3 +/. - c.-74381dup r.(?) p.(=)
MSH3 NM_002439.4 +/. - c.1473dup r.(?) p.(Ile492HisfsTer3)


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