Variant #0000565173 (NC_000018.9:g.57115306_57115307insA, NM_133459.3:c.683_684insT (CCBE1))
Chromosome |
18 |
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.57115306_57115307insA |
DNA change (hg38) |
g.59448074_59448075insA |
Published as |
CCBE1(NM_133459.3):c.683_684insT (p.(Leu229fs)), CCBE1(NM_133459.4):c.683_684insT (p.L229Pfs*8) |
ISCN |
- |
DB-ID |
CCBE1_000014 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) |
5.0E-5 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 |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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