Variant #0000323088 (NC_000012.11:g.111856571G>C, NM_005475.2:c.622G>C (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.111856571G>C
DNA change (hg38) g.111418767G>C
Published as SH2B3(NM_005475.2):c.622G>C (p.E208Q, p.(Glu208Gln)), SH2B3(NM_005475.3):c.622G>C (p.E208Q)
ISCN -
DB-ID SH2B3_000003 See all 5 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) 0.00103 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.622G>C r.(?) p.(Glu208Gln)


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