Variant #0000968312 (NC_000016.9:g.28884062G>A, NC_000016.9(NM_015503.2):c.1897+36G>A (SH2B1))

Chromosome 16
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.28884062G>A
DNA change (hg38) -
Published as SH2B1(NM_001145797.2):c.1933G>A (p.V645M)
ISCN -
DB-ID SH2B1_000041
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) 8.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SH2B1 NM_001387430.1 -?/. - c.1897+36G>A r.(=) p.(=)
SH2B1 NM_015503.2 -?/. - c.1897+36G>A r.(=) p.(=)


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