Variant #0001037670 (NC_000010.10:g.101486911G>C, NM_078470.4:c.396C>G (COX15))

Chromosome 10
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.101486911G>C
DNA change (hg38) -
Published as COX15(NM_078470.6):c.396C>G (p.(Ile132Met))
ISCN -
DB-ID COX15_000026
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) 1.0E-5 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     
COX15 NM_004376.5 ?/. - c.396C>G r.(?) p.(Ile132Met)
CUTC NM_015960.2 ?/. - c.-5195G>C r.(?) p.(=)
ENTPD7 NM_020354.3 ?/. - c.*22471G>C r.(=) p.(=)
COX15 NM_078470.4 ?/. - c.396C>G r.(?) p.(Ile132Met)


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