Variant #0000911386 (NC_000002.11:g.179556748G>T, NM_001267550.1:c.31757C>A (TTN))
Chromosome |
2 |
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.179556748G>T |
DNA change (hg38) |
- |
Published as |
TTN(NM_001267550.1):c.31757C>A (p.P10586Q), TTN(NM_001267550.2):c.31757C>A (p.P10586Q, p.(Pro10586Gln)) |
ISCN |
- |
DB-ID |
TTN_002672 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) |
0.00046 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2023-01-11 15:44:22 +01:00 (CET) |
Date last edited |
2024-04-19 20:20:39 +02:00 (CEST) |

Variant on transcripts
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