Variant #0000657667 (NC_000015.9:g.78398150A>C, NM_006383.3:c.473T>G (CIB2))

Chromosome 15
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.78398150A>C
DNA change (hg38) g.78105808A>C
Published as CIB2(NM_001301224.1):c.488T>G (p.L163W)
ISCN -
DB-ID SH2D7_000007
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) 0.00011 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SH2D7 NM_001101404.1 ?/. - c.*2293A>C r.(=) p.(=)
CIB2 NM_006383.3 ?/. - c.473T>G r.(?) p.(Leu158Trp)


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