Variant #0000332578 (NC_000009.11:g.15465565_15465566del, NM_033222.3:c.1554_1555del (PSIP1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.15465565_15465566del
DNA change (hg38) g.15465567_15465568del
Published as PSIP1(NM_033222.5):c.1554_1555del (p.(Glu518Aspfs*2))
ISCN -
DB-ID PSIP1_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNAPC3 NM_001039697.1 ?/. - c.*5701_*5702del r.(=) p.(=)
PSIP1 NM_033222.3 ?/. - c.1554_1555del r.(?) p.(Glu518AspfsTer2)


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