Variant #0000926123 (NC_000016.9:g.1397757C>T, NM_032520.4:c.-4210C>T (GNPTG))

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.1397757C>T
DNA change (hg38) -
Published as BAIAP3(NM_001199096.1):c.2852C>T (p.(Ala951Val))
ISCN -
DB-ID BAIAP3_000015
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) 0.00015 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 2023-04-16 21:50:28 +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     
TSR3 NM_001001410.2 -?/. - c.*1681G>A r.(=) p.(=)
BAIAP3 NM_001199096.1 -?/. - c.2852C>T r.(?) p.(Ala951Val)
GNPTG NM_032520.4 -?/. - c.-4210C>T r.(?) p.(=)


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