Variant #0000886921 (NC_000005.9:g.80150127A>G, NM_002439.4:c.2992A>G (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.80150127A>G
DNA change (hg38) -
Published as MSH3(NM_002439.5):c.2992A>G (p.I998V)
ISCN -
DB-ID DHFR_000084
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) 0.0002 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +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.-199819T>C r.(?) p.(=)
MSH3 NM_002439.4 ?/. - c.2992A>G r.(?) p.(Ile998Val)


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