Variant #0000997785 (NC_000009.11:g.15423106G>C, NM_033222.3:c.*42412C>G (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.15423106G>C
DNA change (hg38) -
Published as SNAPC3(NM_001039697.1):c.229G>C (p.(Ala77Pro))
ISCN -
DB-ID PSIP1_000006
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 2024-08-28 13:16:32 +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.229G>C r.(?) p.(Ala77Pro)
PSIP1 NM_033222.3 -?/. - c.*42412C>G r.(=) p.(=)


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