Variant #0000508364 (NC_000001.10:g.76346921_76346922insAT, NC_000001.10(NM_002440.3):c.1782-10_1782-9insAT (MSH4))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76346921_76346922insAT
DNA change (hg38) g.75881236_75881237insAT
Published as MSH4(NM_002440.4):c.1782-10_1782-9insAT
ISCN -
DB-ID MSH4_000003
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH4 NM_002440.3 -?/. - c.1782-10_1782-9insAT r.(=) p.(=)


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