Variant #0000523919 (NC_000005.9:g.122425871_122425876dup, NM_001136239.1:c.162_167dup (PRDM6))

Chromosome 5
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.122425871_122425876dup
DNA change (hg38) g.123090176_123090181dup
Published as PRDM6(NM_001136239.1):c.152_153insGCCGCC (p.(Gln51_Pro52insProPro)), PRDM6(NM_001136239.3):c.162_167dupGCCGCC (p.P58_P59dup), PRDM6(NM_001136239.4)...
ISCN -
DB-ID PRDM6_000002 See all 3 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_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 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRDM6 NM_001136239.1 ?/. - c.162_167dup r.(?) p.(Pro58_Pro59dup)


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