Variant #0000401452 (NC_000016.9:g.2546265C>T, NM_001199107.1:c.116C>T (TBC1D24))
Chromosome |
16 |
Allele |
Paternal (confirmed) |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2546265C>T |
DNA change (hg38) |
g.2496264C>T |
Published as |
- |
ISCN |
- |
DB-ID |
TBC1D24_000070 See all 7 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Somatic |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
Owner |
Jing Zhang |
Database submission license |
No license selected |
Created by |
Jing Zhang |
Date created |
2018-08-19 13:03:10 +02:00 (CEST) |
Date last edited |
2018-08-22 18:28:21 +02:00 (CEST) |

Variant on transcripts
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