Variant #0000982481 (NC_000017.10:g.40336520_40336522dup, NM_012285.2:c.-3540_-3538dup (KCNH4))

Chromosome 17
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.40336520_40336522dup
DNA change (hg38) -
Published as HCRT(NM_001524.1):c.65_67dup (p.(Leu22dup))
ISCN -
DB-ID GHDC_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HCRT NM_001524.1 -?/. - c.65_67dup r.(?) p.(Leu22dup)
KCNH4 NM_012285.2 -?/. - c.-3540_-3538dup r.(?) p.(=)
GHDC NM_032484.4 -?/. - c.*5218_*5220dup r.(=) p.(=)


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