Variant #0001040771 (NC_000016.9:g.1398002G>A, NM_032520.4:c.-3965G>A (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.1398002G>A
DNA change (hg38) -
Published as BAIAP3(NM_001199097.2):c.3133G>A (p.(Asp1045Asn))
ISCN -
DB-ID BAIAP3_000024
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 2025-05-05 21:14:00 +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.*1436C>T r.(=) p.(=)
BAIAP3 NM_001199096.1 ?/. - c.3025G>A r.(?) p.(Asp1009Asn)
GNPTG NM_032520.4 ?/. - c.-3965G>A r.(?) p.(=)


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