Variant #0000357453 (NC_000002.11:g.48033551C>G, NC_000002.11(NM_000179.2):c.3802-40C>G (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48033551C>G
DNA change (hg38) g.47806412C>G
Published as -
ISCN -
DB-ID MSH6_000270 See all 47 reported entries
Variant remarks Insight class: 1
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.73326 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 -/- 8i c.3802-40C>G r.(=) p.(=)


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