Variant #0000615545 (NC_000015.9:g.78398175C>T, NM_006383.3:c.448G>A (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.78398175C>T
DNA change (hg38) g.78105833C>T
Published as CIB2(NM_001301224.1):c.463G>A (p.D155N)
ISCN -
DB-ID SH2D7_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) 0.002 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 2019-12-04 15:24:38 +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.*2318C>T r.(=) p.(=)
CIB2 NM_006383.3 ?/. - c.448G>A r.(?) p.(Asp150Asn)


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