Variant #0000308023 (NC_000012.11:g.111872810_111872812del, NC_000012.11(NM_005475.2):c.733-11747_733-11745del (SH2B3))

Chromosome 12
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.111872810_111872812del
DNA change (hg38) g.111435006_111435008del
Published as SH2B3(NM_001291424.1):c.105_107delTCT (p.L36del)
ISCN -
DB-ID SH2B3_000004
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
SH2B3 NM_005475.2 ?/. - c.733-11747_733-11745del r.(=) p.(=)


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