Variant #0000607479 (NC_000002.11:g.219204562G>T, NM_001077399.2:c.*67077G>T (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.219204562G>T
DNA change (hg38) g.218339839G>T
Published as PNKD(NM_015488.4):c.293G>T (p.(Arg98Leu))
ISCN -
DB-ID PNKD_000014
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) 0.0001 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
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     
PNKD NM_001077399.2 ?/. - c.*67077G>T r.(=) p.(=)
TMBIM1 NM_022152.4 ?/. - c.-47414C>A r.(?) p.(=)


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