Variant #0000992731 (NC_000002.11:g.241679488G>A, NM_004321.6:c.3585C>T (KIF1A))
Chromosome |
2 |
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.241679488G>A |
DNA change (hg38) |
- |
Published as |
KIF1A(NM_001244008.1):c.3888C>T (p.R1296=), KIF1A(NM_001244008.2):c.3888C>T (p.(Arg1296=), p.R1296=), KIF1A(NM_001379631.1):c.3963C>T (p.R1321=) |
ISCN |
- |
DB-ID |
KIF1A_000041 See all 7 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) |
0.00229 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2024-08-28 13:07:21 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|