Variant #0000526135 (NC_000005.9:g.79950567G>A, NM_002439.4:c.21G>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.79950567G>A
DNA change (hg38) g.80654748G>A
Published as DHFR(NM_000791.3):c.-259C>T (p.(=)), MSH3(NM_002439.5):c.21G>A (p.A7=)
ISCN -
DB-ID DHFR_000016 See all 4 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) 0.00783 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHFR NM_000791.3 -/. - c.-259C>T r.(?) p.(=)
MTRNR2L2 NM_001190470.1 -/. - c.-4662C>T r.(?) p.(=)
MSH3 NM_002439.4 -/. - c.21G>A r.(?) p.(Ala7=)


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