Variant #0000617283 (NC_000019.9:g.10395948del, ICAM1(NM_000201.2):c.1584del)

Chromosome 19
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.10395948del
DNA change (hg38) g.10285272del
Published as ICAM1(NM_000201.2):c.1584del (p.(Ala529ProfsTer26))
ISCN -
DB-ID ICAM1_000006
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) Variant not found in online data sets
Owner VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ICAM1 NM_000201.2 ?/. - c.1584del r.(?) p.(Ala529ProfsTer26)
ICAM4 NM_001544.4 ?/. - c.-1741del r.(?) p.(=)
ICAM5 NM_003259.3 ?/. - c.-4772del r.(?) p.(=)