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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RIMBP3C NM_001128633.1 -/. - c.3196_3201dup r.(?) p.(Gln1066_Val1067dup)
UBE2L3 NM_001256355.1 -/. - c.-1672_-1667dup r.(?) p.(=)


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