Variant #0000324608 (NC_000016.9:g.15112742C>T, NM_173474.3:c.*19146G>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.15112742C>T
DNA change (hg38) g.15018885C>T
Published as PDXDC1(NM_015027.2):c.1009C>T (p.(Arg337Cys))
ISCN -
DB-ID PDXDC1_000002
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) 0.00024 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDXDC1 NM_015027.2 ?/. - c.1009C>T r.(?) p.(Arg337Cys)
RRN3 NM_018427.3 ?/. - c.*42859G>A r.(=) p.(=)
NTAN1 NM_173474.3 ?/. - c.*19146G>A r.(=) p.(=)


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