Variant #0000512540 (NC_000002.11:g.179554624C>T, NC_000002.11(NM_001267550.1):c.31763-1G>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.179554624C>T |
DNA change (hg38) |
g.178689897C>T |
Published as |
TTN(NM_001256850.1):c.30812-1G>A (p.(=)), TTN(NM_001267550.1):c.31763-1G>A, TTN(NM_001267550.2):c.31763-1G>A, TTN(NM_133432.3):c.13658-47580G>A |
ISCN |
- |
DB-ID |
TTN_000691 See all 14 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) |
0.00033 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 |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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