Variant #0000555562 (NC_000015.9:g.78398100T>G, NM_006383.3:c.523A>C (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.78398100T>G
DNA change (hg38) g.78105758T>G
Published as CIB2(NM_006383.3):c.523A>C (p.K175Q)
ISCN -
DB-ID SH2D7_000003 See all 2 reported entries
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) 0.00078 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.*2243T>G r.(=) p.(=)
CIB2 NM_006383.3 ?/. - c.523A>C r.(?) p.(Lys175Gln)


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