Variant #0000948584 (NC_000005.9:g.80021325A>G, NM_002439.4:c.1394A>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.80021325A>G
DNA change (hg38) -
Published as MSH3(NM_002439.4):c.1394A>G (p.(Tyr465Cys)), MSH3(NM_002439.5):c.1394A>G (p.Y465C)
ISCN -
DB-ID MSH3_000014 See all 6 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHFR NM_000791.3 ?/. - c.-71017T>C r.(?) p.(=)
MSH3 NM_002439.4 ?/. - c.1394A>G r.(?) p.(Tyr465Cys)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.