Variant #0000555560 (NC_000015.9:g.78393434C>T, NM_006383.3:c.*4219G>A (CIB2))

Chromosome 15
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.78393434C>T
DNA change (hg38) g.78101092C>T
Published as SH2D7(NM_001101404.1):c.839C>T (p.(Ala280Val))
ISCN -
DB-ID SH2D7_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) 0.00363 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     
SH2D7 NM_001101404.1 -?/. - c.839C>T r.(?) p.(Ala280Val)
CIB2 NM_006383.3 -?/. - c.*4219G>A r.(=) p.(=)


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