Variant #0001057126 (NC_000022.10:g.30163542G>C, NM_182527.2:c.*37984G>C (CABP7))

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.30163542G>C
DNA change (hg38) -
Published as UQCR10(NM_001003684.2):c.155G>C (p.(Arg52Thr))
ISCN -
DB-ID CABP7_000002
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UQCR10 NM_013387.3 ?/. - c.150+5G>C r.spl? p.?
ZMAT5 NM_019103.2 ?/. - c.-824C>G r.(?) p.(=)
CABP7 NM_182527.2 ?/. - c.*37984G>C r.(=) p.(=)


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