Variant #0000725736 (NC_000016.9:g.29825199C>T, NM_145239.2:c.824C>T (PRRT2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.29825199C>T
DNA change (hg38) -
Published as PRRT2(NM_001256443.2):c.824C>T (p.S275F)
ISCN -
DB-ID PRRT2_000044 See all 2 reported entries
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAZ NM_002383.2 +?/. - c.*3647C>T r.(=) p.(=)
MVP NM_005115.4 +?/. - c.-6668C>T r.(?) p.(=)
PAGR1 NM_024516.3 +?/. - c.-2648C>T r.(?) p.(=)
PRRT2 NM_145239.2 +?/. - c.824C>T r.(?) p.(Ser275Phe)


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