Variant #0000516273 (NC_000002.11:g.48025785A>C, NM_000179.2:c.663A>C (MSH6))

Chromosome 2
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.48025785A>C
DNA change (hg38) g.47798646A>C
Published as MSH6(NM_000179.2):c.663A>C (p.E221D, p.(Glu221Asp)), MSH6(NM_000179.3):c.663A>C (p.E221D)
ISCN -
DB-ID MSH6_000929 See all 24 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) 0.0007 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 -?/. - c.663A>C r.(?) p.(Glu221Asp)
FBXO11 NM_001190274.1 -?/. - c.*9472T>G r.(=) p.(=)


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