Variant #0000417776 (NC_000002.11:g.48026022_48026023insTC, NM_000179.2:c.900_901insTC (MSH6))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48026022_48026023insTC |
DNA change (hg38) |
g.47798883_47798884insTC |
Published as |
- |
ISCN |
- |
DB-ID |
MSH6_000006 See all 8 reported entries |
Variant remarks |
Frameshift |
Reference |
Sjursen, W., McPhillips, M., Scott, R. J. and Talseth-Palmer, B. A. (2016), Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations. Mol Genet Genomic Med. doi:10.1002/mgg3.198 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
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-NonCommercial-ShareAlike 4.0 International |
Created by |
InSiGHT - John-Paul Plazzer |
Date created |
2016-02-01 06:28:37 +01:00 (CET) |
Date last edited |
2018-11-09 16:06:39 +01:00 (CET) |

Variant on transcripts
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