Variant #0000883483 (NC_000001.10:g.46546396T>C, NM_005727.3:c.-94827T>C (TSPAN1))

Chromosome 1
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.46546396T>C
DNA change (hg38) -
Published as PIK3R3(NM_001114172.1):c.133A>G (p.(Met45Val))
ISCN -
DB-ID PIK3R3_000016
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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIK3R3 NM_003629.3 -?/. - c.133A>G r.(?) p.(Met45Val)
TSPAN1 NM_005727.3 -?/. - c.-94827T>C r.(?) p.(=)


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