Variant #0000267095 (NC_000001.10:g.245006496_245006497insAAGAA, NM_198076.4:c.*18_*19insAAGAA (COX20))

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.245006496_245006497insAAGAA
DNA change (hg38) g.244843194_244843195insAAGAA
Published as COX20(NM_198076.6):c.*18_*19insAAGAA, COX20(NM_198076.6):c.*19delGinsAAGAAG
ISCN -
DB-ID COX20_000005
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
COX20 NM_198076.4 -?/. - c.*18_*19insAAGAA r.(=) p.(=)
HNRNPU-AS1 NR_026778.1 -?/. - n.2492_2493insTTTCT r.(?) -


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