Variant #0000323239 (NC_000012.11:g.132625438C>T, NM_175066.3:c.1378G>A (DDX51))

Chromosome 12
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.132625438C>T
DNA change (hg38) g.132140893C>T
Published as DDX51(NM_175066.3):c.1378G>A (p.(Gly460Ser)), DDX51(NM_175066.4):c.1378G>A (p.G460S)
ISCN -
DB-ID DDX51_000002 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) 0.00028 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
NOC4L NM_024078.1 -?/. - c.-3596C>T r.(?) p.(=)
DDX51 NM_175066.3 -?/. - c.1378G>A r.(?) p.(Gly460Ser)


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