Variant #0000525794 (NC_000005.9:g.45695986_45695994del, NM_021072.3:c.215_223del (HCN1))

Chromosome 5
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.45695986_45695994del
DNA change (hg38) g.45695884_45695892del
Published as HCN1(NM_021072.3):c.215_223delGCGGCGGCG (p.G72_G74del), HCN1(NM_021072.4):c.215_223delGCGGCGGCG (p.G72_G74del)
ISCN -
DB-ID HCN1_000034 See all 3 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
HCN1 NM_021072.3 -?/. - c.215_223del r.(?) p.(Gly72_Gly74del)


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