Variant #0000518362 (NC_000003.11:g.15676984_15676990delinsTCC, BTD(NM_000060.2):c.98_104delinsTCC)
Chromosome |
3 |
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.15676984_15676990delinsTCC |
DNA change (hg38) |
g.15635477_15635483delinsTCC |
Published as |
BTD(NM_000060.4):c.98_104delGCGGCTGinsTCC (p.C33Ffs*36) |
ISCN |
- |
DB-ID |
BTD_000109 See all 5 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) |
Variant not found in online data sets |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |

Variant on transcripts
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