Variant #0001046620 (NC_000017.10:g.37884176C>A, NM_033419.3:c.-39909G>T (PGAP3))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.37884176C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ERBB2_000005 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) 0.00584 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-07-08 13:22:38 +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     
ERBB2 NM_001005862.1 -/. - c.3557C>A r.(?) p.(Ala1186Asp)
MIEN1 NM_032339.3 -/. - c.*1599G>T r.(=) p.(=)
PGAP3 NM_033419.3 -/. - c.-39909G>T r.(?) p.(=)


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