Variant #0001055314 (NC_000016.9:g.1402251_1402267del, NM_032520.4:c.122_138del (GNPTG))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1402251_1402267del
DNA change (hg38) -
Published as GNPTG(NM_032520.5):c.122_138del (p.(Pro41Glnfs*36))
ISCN -
DB-ID GNPTG_000039 See all 2 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) 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 2025-11-01 13:22:20 +01:00 (CET)
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.-460_-444del r.(?) p.(=)
BAIAP3 NM_001199096.1 +?/. - c.*3768_*3784del r.(=) p.(=)
GNPTG NM_032520.4 +?/. - c.122_138del r.(?) p.(Pro41Glnfs*36)


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