Variant #0000537858 (NC_000009.11:g.27062666G>A, NM_001031689.2:c.-115623C>T (PLAA))
| Chromosome |
9 |
| 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.27062666G>A |
| DNA change (hg38) |
g.27062668G>A |
| Published as |
IFT74(NM_001099222.2):c.1735G>A (p.V579M), IFT74(NM_001099222.3):c.1735G>A (p.V579M), IFT74(NM_025103.3):c.1735G>A (p.V579M), IFT74(NM_025103.4):c.... |
| ISCN |
- |
| DB-ID |
IFT74_000007 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) |
0.00548 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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