Variant #0000526568 (NC_000006.11:g.105300263_105300264insGA, NC_000006.11(NM_020771.3):c.77-17_77-16insCT (HACE1))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.105300263_105300264insGA
DNA change (hg38) g.104852388_104852389insGA
Published as HACE1(NM_020771.4):c.77-17_77-16insCT
ISCN -
DB-ID HACE1_000010
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) 0.66226 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HACE1 NM_020771.3 -/. - c.77-17_77-16insCT r.(=) p.(=)


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