Variant #0000966883 (NC_000012.11:g.39726207G>A, NM_001173464.1:c.2860C>T (KIF21A))
Chromosome |
12 |
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.39726207G>A |
DNA change (hg38) |
- |
Published as |
KIF21A(NM_001173464.2):c.2860C>T (p.(Arg954Trp)), KIF21A(NM_017641.4):c.2821C>T (p.R941W) |
ISCN |
- |
DB-ID |
KIF21A_000016 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) |
Retrieve |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2024-02-26 20:06:56 +01:00 (CET) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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