Full data view for gene ICAM1

Information The variants shown are described using the NM_000201.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/. - c.1405A>G r.(?) p.(Lys469Glu) Unknown - benign g.10395683A>G g.10285007A>G ICAM1(NM_000201.2):c.1405A>G (p.K469E) - ICAM1_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
./. - c.1405A>G r.(?) p.(Lys469Glu) Unknown - VUS g.10395683A>G g.10285007A>G - - ICAM1_000003 for details see the Uveogene database PubMed: Park 2003 - rs5498 Germline - 160/394 cases - 0 - DNA arraySNP Blood - Behcet - PubMed: Park 2003 Korean cohortcohort F;M - Korea Korean - 0 for details see the Uveogene database - 160 Peizeng Yang
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