Variant #0000324962 (NC_000016.9:g.87637930_87637935dup, NC_000016.9(NM_020655.2):c.382+796_382+801dup (JPH3))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.87637930_87637935dup |
DNA change (hg38) |
g.87604324_87604329dup |
Published as |
JPH3(NM_001271604.2):c.431_436dup (p.(Ala145_Ala146dup)), JPH3(NM_001271604.2):c.467_472dupCTGCTG (p.A156_A157dup), JPH3(NM_001271604.4):c.467_472d... |
ISCN |
- |
DB-ID |
JPH3_000006 |
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) |
Retrieve |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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