Variant #0000689286 (NC_000004.11:g.20731737G>A, NM_025221.5:c.721C>T (KCNIP4))

Chromosome 4
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.20731737G>A
DNA change (hg38) -
Published as KCNIP4(NM_001035003.1):c.646C>T (p.R216C)
ISCN -
DB-ID KCNIP4_000002
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) 3.0E-5 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 2020-09-15 15:50:26 +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     
KCNIP4 NM_025221.5 -?/. - c.721C>T r.(?) p.(Arg241Cys)
PACRGL NM_145048.3 -?/. - c.*2773G>A r.(=) p.(=)


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