Variant #0000320471 (NC_000001.10:g.2436319_2436322del, NM_018216.1:c.*3966_*3969del (PANK4))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2436319_2436322del
DNA change (hg38) g.2504880_2504883del
Published as PLCH2(NM_014638.2):c.3916_3919del (p.(Thr1307SerfsTer190))
ISCN -
DB-ID PLCH2_000006
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLCH2 NM_014638.2 ?/. - c.3918_3921del r.(?) p.(Thr1307SerfsTer190)
PANK4 NM_018216.1 ?/. - c.*3966_*3969del r.(=) p.(=)


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