Variant #0000510556 (NC_000002.11:g.179399576C>G, NM_001267550.1:c.101766G>C (TTN))
Chromosome |
2 |
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.179399576C>G |
DNA change (hg38) |
g.178534849C>G |
Published as |
TTN(NM_001256850.1):c.96843G>C (p.(Gln32281His)), TTN(NM_001267550.1):c.101766G>C (p.Q33922H), TTN(NM_001267550.2):c.101766G>C (p.Q33922H), TTN(NM...) |
ISCN |
- |
DB-ID |
TTN_000454 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) |
0.00718 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
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
|