Variant #0000278577 (NC_000001.10:g.10363487T>C, NC_000001.10(NM_015074.3):c.1977+6183T>C (KIF1B))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.10363487T>C |
DNA change (hg38) |
g.10303429T>C |
Published as |
KIF1B(NM_001365953.1):c.2244T>C (p.A748=), KIF1B(NM_183416.4):c.2244T>C (p.A748=) |
ISCN |
- |
DB-ID |
KIF1B_000028 See all 3 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) |
0.00348 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
|