Variant #0000615633 (NC_000015.9:g.90196146G>A, NM_198525.2:c.16C>T (KIF7))
Chromosome |
15 |
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.90196146G>A |
DNA change (hg38) |
g.89652915G>A |
Published as |
KIF7(NM_198525.2):c.16C>T (p.Q6*) |
ISCN |
- |
DB-ID |
KIF7_000152 |
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) |
1.0E-5 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2020-07-07 09:38:02 +02:00 (CEST) |

Variant on transcripts
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