Variant #0000512510 (NC_000002.11:g.179549407G>A, NM_001267550.1:c.32624C>T (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.179549407G>A |
| DNA change (hg38) |
g.178684680G>A |
| Published as |
TTN(NM_001256850.1):c.31673C>T (p.(Pro10558Leu)), TTN(NM_001267550.1):c.32624C>T (p.P10875L), TTN(NM_001267550.2):c.32624C>T (p.P10875L) |
| ISCN |
- |
| DB-ID |
TTN_000931 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) |
0.00543 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 |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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