Variant #0000692326 (NC_000017.10:g.37883696C>T, PGAP3(NM_033419.3):c.-39429G>A)

Chromosome 17
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.37883696C>T
DNA change (hg38) -
Published as ERBB2(NM_001289936.1):c.3263C>T (p.T1088I)
ISCN -
DB-ID ERBB2_000017
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERBB2 NM_001005862.1 -?/. - c.3218C>T r.(?) p.(Thr1073Ile)
MIEN1 NM_032339.3 -?/. - c.*2079G>A r.(=) p.(=)
PGAP3 NM_033419.3 -?/. - c.-39429G>A r.(?) p.(=)