Variant #0001064348 (NC_000005.9:g.79950708_79950717del, NM_002439.4:c.162_171del (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.79950708_79950717del
DNA change (hg38) -
Published as -
ISCN -
DB-ID DHFR_000118
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
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.-408_-399del r.(?) p.(=)
MTRNR2L2 NM_001190470.1 -?/. - c.-4811_-4802del r.(?) p.(=)
MSH3 NM_002439.4 -?/. - c.162_171del r.(?) p.(Ala55Glnfs*22)


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