Variant #0000555448 (NC_000015.9:g.73660154T>C, NM_005477.2:c.458A>G (HCN4))

Chromosome 15
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.73660154T>C
DNA change (hg38) g.73367813T>C
Published as HCN4(NM_005477.2):c.458A>G (p.E153G), HCN4(NM_005477.3):c.458A>G (p.E153G)
ISCN -
DB-ID HCN4_000141 See all 4 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) 0.00206 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
HCN4 NM_005477.2 -?/. - c.458A>G r.(?) p.(Glu153Gly)


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