Variant #0000963700 (NC_000005.9:g.80168918C>T, NC_000005.9(NM_002439.4):c.3131-17C>T (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.80168918C>T
DNA change (hg38) -
Published as MSH3(NM_002439.4):c.3131-17C>T (p.(=))
ISCN -
DB-ID DHFR_000098
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) 8.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-02-26 20:06:56 +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.-218610G>A r.(?) p.(=)
MSH3 NM_002439.4 ?/. - c.3131-17C>T r.(=) p.(=)


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