Variant #0000802185 (NC_000005.9:g.79924975A>C, NM_002439.4:c.-25572A>C (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.79924975A>C
DNA change (hg38) -
Published as DHFR(NM_000791.4):c.495T>G (p.G165=)
ISCN -
DB-ID DHFR_000075
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +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.495T>G r.(?) p.(Gly165=)
MTRNR2L2 NM_001190470.1 -?/. - c.*20844T>G r.(=) p.(=)
MSH3 NM_002439.4 -?/. - c.-25572A>C r.(?) p.(=)


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