Variant #0000250146 (NC_000009.11:g.26978168A>T, NM_001031689.2:c.-31125T>A (PLAA))
| Chromosome |
9 |
| 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.26978168A>T |
| DNA change (hg38) |
g.26978170A>T |
| Published as |
IFT74(NM_001099222.2):c.163A>T (p.I55L), IFT74(NM_001099222.3):c.163A>T (p.I55L), IFT74(NM_001349928.2):c.163A>T (p.I55L), IFT74(NM_025103.4):c.163... |
| ISCN |
- |
| DB-ID |
IFT74_000001 See all 4 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) |
0.00104 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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