Variant #0000292030 (NC_000005.9:g.79950741_79950749del, NM_002439.4:c.195_203del (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.79950741_79950749del
DNA change (hg38) g.80654922_80654930del
Published as DHFR(NM_000791.4):c.-428_-420delGGGGCGCTG, MSH3(NM_002439.4):c.195_203delGCCCCCAGC (p.P67_P69del), MSH3(NM_002439.5):c.195_203delGCCCCCAGC (p.P67_...)
ISCN -
DB-ID MSH3_000011
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.-428_-420del r.(?) p.(=)
MTRNR2L2 NM_001190470.1 -/. - c.-4831_-4823del r.(?) p.(=)
MSH3 NM_002439.4 -/. - c.195_203del r.(?) p.(Pro67_Pro69del)


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