Variant #0000526155 (NC_000005.9:g.79950745_79950753del, NM_002439.4:c.199_207del (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.79950745_79950753del
DNA change (hg38) g.80654926_80654934del
Published as MSH3(NM_002439.5):c.199_207delCCAGCTCCC (p.P67_P69del)
ISCN -
DB-ID DHFR_000030
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_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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHFR NM_000791.3 -/. - c.-442_-434del r.(?) p.(=)
MTRNR2L2 NM_001190470.1 -/. - c.-4845_-4837del r.(?) p.(=)
MSH3 NM_002439.4 -/. - c.199_207del r.(?) p.(Pro67_Pro69del)


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