Variant #0000514572 (NC_000002.11:g.219204497G>A, NM_001077399.2:c.*67012G>A (PNKD))

Chromosome 2
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.219204497G>A
DNA change (hg38) g.218339774G>A
Published as PNKD(NM_015488.4):c.237-9G>A
ISCN -
DB-ID PNKD_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) 0.00048 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 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     
PNKD NM_001077399.2 -?/. - c.*67012G>A r.(=) p.(=)
TMBIM1 NM_022152.4 -?/. - c.-47349C>T r.(?) p.(=)


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