Variant #0000526143 (NC_000005.9:g.79950724_79950732del, NM_002439.4:c.178_186del (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.79950724_79950732del
DNA change (hg38) g.80654905_80654913del
Published as DHFR(NM_000791.3):c.-409_-401del (p.(=)), DHFR(NM_000791.4):c.-409_-401delGGCCGCTGC, MSH3(NM_002439.4):c.178_186delGCCGCAGCG (p.A60_A62del), MSH3...)
ISCN -
DB-ID DHFR_000022 See all 5 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) 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 2024-02-26 20:06:56 +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.-409_-401del r.(?) p.(=)
MTRNR2L2 NM_001190470.1 -/. - c.-4812_-4804del r.(?) p.(=)
MSH3 NM_002439.4 -/. - c.178_186del r.(?) p.(Ala60_Ala62del)


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