Variant #0000526529 (NC_000006.11:g.100061159_100061162dup, NM_021620.3:c.648_651dup (PRDM13))

Chromosome 6
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.100061159_100061162dup
DNA change (hg38) g.99613283_99613286dup
Published as PRDM13(NM_021620.3):c.648_651dupACCA (p.V218Tfs*235)
ISCN -
DB-ID PRDM13_000009
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-19 19:36:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRDM13 NM_021620.3 ?/. - c.648_651dup r.(?) p.(Val218ThrfsTer235)


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