Variant #0001046035 (NC_000005.9:g.79950724_79950732dup, NM_002439.4:c.178_186dup (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.79950724_79950732dup
DNA change (hg38) -
Published as DHFR(NM_000791.3):c.-409_-401dup (p.(=))
ISCN -
DB-ID DHFR_000113
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 2025-07-08 13:22:38 +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.-409_-401dup r.(?) p.(=)
MTRNR2L2 NM_001190470.1 ?/. - c.-4812_-4804dup r.(?) p.(=)
MSH3 NM_002439.4 ?/. - c.178_186dup r.(?) p.(Ala60_Ala62dup)


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