Variant #0001001902 (NC_000016.9:g.15068803C>G, NM_173474.3:c.*63085G>C (NTAN1))

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.15068803C>G
DNA change (hg38) -
Published as PDXDC1(NM_001285448.1):c.-192C>G (p.?)
ISCN -
DB-ID NTAN1_000003
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) 2.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDXDC1 NM_015027.2 -?/. - c.-254C>G r.(?) p.(=)
RRN3 NM_018427.3 -?/. - c.*86798G>C r.(=) p.(=)
NTAN1 NM_173474.3 -?/. - c.*63085G>C r.(=) p.(=)


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