Variant #0000507733 (NC_000001.10:g.46655645C>T, NM_001243766.1:c.1666G>A (POMGNT1))
| Chromosome |
1 |
| 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.46655645C>T |
| DNA change (hg38) |
g.46189973C>T |
| Published as |
POMGNT1(NM_001243766.1):c.1666G>A (p.(Asp556Asn), p.D556N), POMGNT1(NM_001243766.2):c.1666G>A (p.D556N), POMGNT1(NM_017739.3):c.1666G>A (p.D556N) |
| ISCN |
- |
| DB-ID |
POMGNT1_000035 See all 10 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) |
0.00991 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 |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|