Variant #0000992498 (NC_000002.11:g.219204581_219204585del, NM_001077399.2:c.*67096_*67100del (PNKD))

Chromosome 2
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.219204581_219204585del
DNA change (hg38) -
Published as PNKD(NM_015488.4):c.312_316delCCCTA (p.(Tyr104fs))
ISCN -
DB-ID PNKD_000024
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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PNKD NM_001077399.2 ?/. - c.*67096_*67100del r.(=) p.(=)
TMBIM1 NM_022152.4 ?/. - c.-47434_-47430del r.(?) p.(=)


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