Variant #0000247417 (NC_000016.9:g.1402290A>T, NM_032520.4:c.161A>T (GNPTG))

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.1402290A>T
DNA change (hg38) g.1352289A>T
Published as GNPTG(NM_032520.4):c.161A>T (p.(Asp54Val)), GNPTG(NM_032520.5):c.161A>T (p.D54V)
ISCN -
DB-ID GNPTG_000011 See all 3 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) 0.00016 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSR3 NM_001001410.2 ?/. - c.-485T>A r.(?) p.(=)
BAIAP3 NM_001199096.1 ?/. - c.*3807A>T r.(=) p.(=)
GNPTG NM_032520.4 ?/. 3 c.161A>T r.(?) p.(Asp54Val)


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