Variant #0000526171 (NC_000005.9:g.80063896C>T, NM_002439.4:c.2041C>T (MSH3))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.80063896C>T
DNA change (hg38) g.80768077C>T
Published as MSH3(NM_002439.4):c.2041C>T (p.P681S, p.(Pro681Ser)), MSH3(NM_002439.5):c.2041C>T (p.P681S)
ISCN -
DB-ID DHFR_000045 See all 7 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) 0.00076 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +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.-113588G>A r.(?) p.(=)
MSH3 NM_002439.4 -?/. - c.2041C>T r.(?) p.(Pro681Ser)


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