Variant #0000551254 (NC_000014.8:g.102900798T>G, NM_014844.3:c.1644T>G (TECPR2))
Chromosome |
14 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.102900798T>G |
DNA change (hg38) |
g.102434461T>G |
Published as |
TECPR2(NM_001172631.1):c.1644T>G (p.(Asn548Lys)), TECPR2(NM_014844.4):c.1644T>G (p.N548K) |
ISCN |
- |
DB-ID |
TECPR2_000035 See all 3 reported entries |
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) |
0.00096 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-11-30 11:21:54 +01:00 (CET) |

Variant on transcripts
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