Variant #0000690602 (NC_000009.11:g.91616917G>T, NM_016848.5:c.*11445C>A (SHC3))

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.91616917G>T
DNA change (hg38) -
Published as S1PR3(NM_005226.4):c.802G>T (p.A268S)
ISCN -
DB-ID C9orf47_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) 4.0E-5 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 2020-09-15 15:50:26 +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     
C9orf47 NM_001001938.3 ?/. - c.*10014G>T r.(=) p.(=)
S1PR3 NM_005226.3 ?/. - c.802G>T r.(?) p.(Ala268Ser)
SHC3 NM_016848.5 ?/. - c.*11445C>A r.(=) p.(=)


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