Variant #0000854276 (NC_000016.9:g.1402124C>A, NM_032520.4:c.74C>A (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.1402124C>A
DNA change (hg38) -
Published as GNPTG(NM_032520.4):c.74C>A (p.(Ala25Glu))
ISCN -
DB-ID GNPTG_000008 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 2022-05-09 15:47:41 +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.-319G>T r.(?) p.(=)
BAIAP3 NM_001199096.1 -?/. - c.*3641C>A r.(=) p.(=)
GNPTG NM_032520.4 -?/. - c.74C>A r.(?) p.(Ala25Glu)


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