Variant #0000804049 (NC_000009.11:g.15466799G>A, NM_033222.3:c.1479C>T (PSIP1))

Chromosome 9
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.15466799G>A
DNA change (hg38) -
Published as PSIP1(NM_001128217.2):c.1479C>T (p.N493=)
ISCN -
DB-ID PSIP1_000002
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) 0.0003 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 2021-09-17 14:40:49 +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     
SNAPC3 NM_001039697.1 -?/. - c.*6935G>A r.(=) p.(=)
PSIP1 NM_033222.3 -?/. - c.1479C>T r.(?) p.(Asn493=)


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