Variant #0000356963 (NC_000002.11:g.48018275A>G, NC_000002.11(NM_000179.2):c.457+13A>G (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.48018275A>G
DNA change (hg38) g.47791136A>G
Published as -
ISCN -
DB-ID MSH6_000030 See all 29 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) Retrieve
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 -?/-? 2i c.457+13A>G r.(=) p.(=)


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