Variant #0000289471 (NC_000002.11:g.27693802G>C, NM_015662.1:c.1685C>G (IFT172))
| 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.27693802G>C |
| DNA change (hg38) |
g.27470935G>C |
| Published as |
IFT172(NM_015662.1):c.1685C>G (p.(Thr562Ser)), IFT172(NM_015662.2):c.1685C>G (p.T562S), IFT172(NM_015662.3):c.1685C>G (p.T562S) |
| ISCN |
- |
| DB-ID |
IFT172_000018 See all 5 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) |
0.00652 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2022-05-09 15:51:19 +02:00 (CEST) |

Variant on transcripts
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