Variant #0000516968 (NC_000002.11:g.74648929G>A, NM_001015055.1:c.*4441C>T (RTKN))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74648929G>A
DNA change (hg38) g.74421802G>A
Published as WDR54(NM_001320825.1):c.52G>A (p.D18N)
ISCN -
DB-ID C2orf81_000001
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) 0.00036 View details
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 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RTKN NM_001015055.1 -/. - c.*4441C>T r.(=) p.(=)
C2orf81 NM_001145054.1 -/. - c.-4394C>T r.(?) p.(=)
WDR54 NM_032118.2 -/. - c.-16G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.