Variant #0000281490 (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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
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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