Variant #0000555546 (NC_000015.9:g.77327859C>T, NM_003978.3:c.940C>T (PSTPIP1))

Chromosome 15
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.77327859C>T
DNA change (hg38) g.77035518C>T
Published as PSTPIP1(NM_003978.3):c.940C>T (p.L314=)
ISCN -
DB-ID PSTPIP1_000049
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) 0.00095 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-06 17:22:09 +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.940C>T r.(?) p.(Leu314=)


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