Variant #0001025133 (NC_000005.9:g.79951030G>A, NC_000005.9(NM_002439.4):c.237+247G>A (MSH3))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.79951030G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID DHFR_000108
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-02-07 18:57:27 +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.-722C>T r.(?) p.(=)
MTRNR2L2 NM_001190470.1 -/. - c.-5125C>T r.(?) p.(=)
MSH3 NM_002439.4 -/. - c.237+247G>A r.(=) p.(=)


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