Variant #0000546140 (NC_000011.9:g.95578325_95578326insTAATATGTTCTAGCCAATGAGTAGATTCCAAGTTAGACAACCAGTGGGTTTCCTCAATGTTGG, NC_000011.9(NM_016156.5):c.1180-3_1180-2insCCAACATTGAGGAAACCCACTGGTTGTCTAACTTGGAATCTACTCATTGGCTAGAACATATTA (MTMR2))
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.95578325_95578326insTAATATGTTCTAGCCAATGAGTAGATTCCAAGTTAGACAACCAGTGGGTTTCCTCAATGTTGG |
DNA change (hg38) |
g.95845161_95845162insTAATATGTTCTAGCCAATGAGTAGATTCCAAGTTAGACAACCAGTGGGTTTCCTCAATGTTGG |
Published as |
MTMR2(NM_001243571.2):c.964-2_964-1ins63 |
ISCN |
- |
DB-ID |
MTMR2_000046 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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