Variant #0000557807 (NC_000016.9:g.29821438_29821452del, NM_145239.2:c.-2272_-2258del (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.29821438_29821452del
DNA change (hg38) g.29810117_29810131del
Published as MAZ(NM_001042539.1):c.*46_*60del (p.(=))
ISCN -
DB-ID PRRT2_000054
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAZ NM_002383.2 -?/. - c.1320_1334del r.(?) p.(Ala444_Ala448del)
KIF22 NM_007317.2 -?/. - c.*4807_*4821del r.(=) p.(=)
PRRT2 NM_145239.2 -?/. - c.-2272_-2258del r.(?) p.(=)


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