Variant #0000975135 (NC_000002.11:g.241679488G>A, NM_001244008.1:c.3888C>T (KIF1A))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2024-04-19 20:20:39 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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