Variant #0001001903 (NC_000016.9:g.15122854C>T, NM_173474.3:c.*9034G>A (NTAN1))

Chromosome 16
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.15122854C>T
DNA change (hg38) -
Published as PDXDC1(NM_001285450.1):c.1255C>T (p.(Gln419*))
ISCN -
DB-ID NTAN1_000004
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_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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDXDC1 NM_015027.2 ?/. - c.1293+31C>T r.(=) p.(=)
RRN3 NM_018427.3 ?/. - c.*32747G>A r.(=) p.(=)
NTAN1 NM_173474.3 ?/. - c.*9034G>A r.(=) p.(=)


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