Variant #0000297398 (NC_000016.9:g.29825242T>A, NM_145239.2:c.867T>A (PRRT2))

Chromosome 16
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.29825242T>A
DNA change (hg38) g.29813921T>A
Published as PRRT2(NM_001256443.2):c.867T>A (p.A289=)
ISCN -
DB-ID PRRT2_000037
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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.*3690T>A r.(=) p.(=)
MVP NM_005115.4 -?/. - c.-6625T>A r.(?) p.(=)
PAGR1 NM_024516.3 -?/. - c.-2605T>A r.(?) p.(=)
PRRT2 NM_145239.2 -?/. - c.867T>A r.(?) p.(Ala289=)


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