Variant #0000680787 (NC_000017.10:g.15930801_15930805del, TTC19(NM_017775.3):c.1108_1112del)
Chromosome |
17 |
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.15930801_15930805del |
DNA change (hg38) |
- |
Published as |
TTC19(NM_001271420.1):c.787_791delAAAAG (p.K263*) |
ISCN |
- |
DB-ID |
NCOR1_000014 |
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) |
Variant not found in online data sets |
Owner |
VKGL-NL_Rotterdam |

Variant on transcripts
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