Variant #0001013523 (NC_000002.11:g.179514069A>C, NC_000002.11(NM_001267550.1):c.39974-11T>G (TTN))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.179514069A>C |
DNA change (hg38) |
- |
Published as |
TTN(NM_001267550.2):c.39974-11T>G |
ISCN |
- |
DB-ID |
TTN_003625 See all 16 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) |
5.0E-5 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2024-10-29 20:49:11 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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