Variant #0000558719 (NC_000016.9:g.67314075T>C, NM_001100915.1:c.*9397A>G (KCTD19))

Chromosome 16
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.67314075T>C
DNA change (hg38) g.67280172T>C
Published as PLEKHG4(NM_001129727.2):c.128T>C (p.V43A)
ISCN -
DB-ID KCTD19_000004
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_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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCTD19 NM_001100915.1 -?/. - c.*9397A>G r.(=) p.(=)
PLEKHG4 NM_015432.3 -?/. - c.128T>C r.(?) p.(Val43Ala)


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