Variant #0000507727 (NC_000001.10:g.46532657G>T, NM_005727.3:c.-108566G>T (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.46532657G>T
DNA change (hg38) g.46066985G>T
Published as PIK3R3(NM_001114172.1):c.421C>A (p.(His141Asn))
ISCN -
DB-ID PIK3R3_000011
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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIK3R3 NM_003629.3 -?/. - c.421C>A r.(?) p.(His141Asn)
TSPAN1 NM_005727.3 -?/. - c.-108566G>T r.(?) p.(=)


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