Variant #0000809244 (NC_000020.10:g.3903933A>G, NM_153638.2:c.1705A>G (PANK2))

Chromosome 20
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.3903933A>G
DNA change (hg38) -
Published as PANK2(NM_001324191.1):c.832A>G (p.I278V)
ISCN -
DB-ID RNF24_000002
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF24 NM_001134337.1 ?/. - c.*10777T>C r.(=) p.(=)
PANK2 NM_153638.2 ?/. - c.1705A>G r.(?) p.(Ile569Val)


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