Variant #0000570534 (NC_000021.8:g.34648907G>A, NM_000628.4:c.180G>A (IL10RB))
Chromosome |
21 |
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.34648907G>A |
DNA change (hg38) |
g.33276602G>A |
Published as |
IL10RB(NM_000628.3):c.180G>A (p.R60=) |
ISCN |
- |
DB-ID |
IL10RB_000003 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) |
Retrieve |
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 |
2020-07-16 22:06:32 +02:00 (CEST) |

Variant on transcripts
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