Variant #0000306568 (NC_000015.9:g.77310807G>A, NM_003978.3:c.147G>A (PSTPIP1))

Chromosome 15
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.77310807G>A
DNA change (hg38) g.77018466G>A
Published as PSTPIP1(NM_001321136.1):c.120G>A (p.A40=), PSTPIP1(NM_003978.3):c.147G>A (p.A49=)
ISCN -
DB-ID PSTPIP1_000002 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) 0.00244 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-06 17:18:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSTPIP1 NM_003978.3 -?/. - c.147G>A r.(?) p.(Ala49=)


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