Variant #0000536340 (NC_000009.11:g.130588091C>T, NM_000118.3:c.572G>A (ENG))
Chromosome |
9 |
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.130588091C>T |
DNA change (hg38) |
g.127825812C>T |
Published as |
ENG(NM_000118.3):c.572G>A (p.G191D), ENG(NM_000118.4):c.572G>A (p.G191D), ENG(NM_001114753.2):c.572G>A (p.(Gly191Asp), p.G191D) |
ISCN |
- |
DB-ID |
ENG_000008 See all 7 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) |
0.00874 View details |
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 |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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