Variant #0000618491 (NC_000022.10:g.21902067_21902072dup, NM_001128633.1:c.3196_3201dup (RIMBP3C))
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.21902067_21902072dup |
DNA change (hg38) |
g.21547778_21547783dup |
Published as |
RIMBP3C(NM_001128633.1):c.3196_3201dupCAGGTG (p.Q1066_V1067dup), RIMBP3C(NM_001128633.1):c.3201_3202insCAGGTG (p.(Gln1066_Val1067dup)) |
ISCN |
- |
DB-ID |
RIMBP3C_000004 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 |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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