Variant #0000074656 (NC_000007.13:g.6035323_6035324insJN866832.1, NC_000007.13(NM_000535.6):c.804-60_804-59insJN866832.1 (PMS2))
Chromosome |
7 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6035323_6035324insJN866832.1 |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
PMS2_000242 See all 2 reported entries |
Variant remarks |
Insight class: 5 Variant Error [ESYNTAX]: This genomic variant has an error (char 33: Syntax error). Please fix this entry and then remove this message. |
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 International |
Created by |
Julia Lopez |
Date created |
2015-07-20 15:58:19 +02:00 (CEST) |
Date last edited |
2019-02-22 12:22:30 +01:00 (CET) |

Variant on transcripts
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