Variant #0001032224 (NC_000001.10:g.89427821A>G, NM_001008661.2:c.461T>C (CCBL2))

Chromosome 1
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.89427821A>G
DNA change (hg38) -
Published as KYAT3(NM_001008661.3):c.461T>C (p.(Leu154Pro))
ISCN -
DB-ID CCBL2_000004
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) 0.00089 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCBL2 NM_001008661.2 -?/. - c.461T>C r.(?) p.(Leu154Pro)
RBMXL1 NM_019610.5 -?/. - c.*20516T>C r.(=) p.(=)


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