Variant #0000328914 (NC_000022.10:g.21982916C>G, NM_001128633.1:c.-77651G>C (RIMBP3C))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.21982916C>G
DNA change (hg38) g.21628627C>G
Published as YDJC(NM_001017964.1):c.763G>C (p.(Gly255Arg))
ISCN -
DB-ID YDJC_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YDJC NM_001017964.1 ?/. - c.763G>C r.(?) p.(Gly255Arg)
RIMBP3C NM_001128633.1 ?/. - c.-77651G>C r.(?) p.(=)
UBE2L3 NM_001256355.1 ?/. - c.*6958C>G r.(=) p.(=)
SDF2L1 NM_022044.2 ?/. - c.-13710C>G r.(?) p.(=)
CCDC116 NM_152612.2 ?/. - c.-4263C>G r.(?) p.(=)


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