Variant #0000805559 (NC_000012.11:g.120878250_120878254del, NC_000012.11(NM_004373.3):c.247-7_247-3del (COX6A1))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.120878250_120878254del
DNA change (hg38) -
Published as COX6A1(NM_004373.4):c.247-7_247-3delTCCAC
ISCN -
DB-ID COX6A1_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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX6A1 NM_004373.3 +?/. - c.247-7_247-3del r.spl? p.?
TRIAP1 NM_016399.2 +?/. - c.*4424_*4428del r.(=) p.(=)


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