Variant #0000356969 (NC_000002.11:g.48032098A>T, NM_000179.2:c.3488A>T (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48032098A>T
DNA change (hg38) g.47804959A>T
Published as -
ISCN -
DB-ID MSH6_000511 See all 25 reported entries
Variant remarks Insight class: 2
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00099 View details
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2018-03-08 19:39:55 +01:00 (CET)
Date last edited 2018-11-09 16:06:39 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 -?/-? 6 c.3488A>T r.(?) p.(Glu1163Val)


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