Variant #0000513005 (NC_000002.11:g.179598553T>G, NM_001267550.1:c.15563A>C (TTN))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.179598553T>G |
DNA change (hg38) |
g.178733826T>G |
Published as |
TTN(NM_001256850.1):c.14612A>C (p.(Gln4871Pro)), TTN(NM_001267550.1):c.15563A>C (p.Q5188P), TTN(NM_001267550.2):c.15563A>C (p.Q5188P) |
ISCN |
- |
DB-ID |
TTN_000776 See all 9 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) |
0.00101 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

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