Variant #0000886032 (NC_000003.11:g.9972602G>A, NM_015513.4:c.-3521G>A (CRELD1))
Chromosome |
3 |
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.9972602G>A |
DNA change (hg38) |
- |
Published as |
IL17RC(NM_153461.3):c.1575G>A (p.A525=), IL17RC(NM_153461.4):c.1575G>A (p.A525=) |
ISCN |
- |
DB-ID |
IL17RC_000048 See all 2 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) |
0.00113 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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