Variant #0000248816 (NC_000019.9:g.10395683A>G, ICAM1(NM_000201.2):c.1405A>G)

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.10395683A>G
DNA change (hg38) g.10285007A>G
Published as ICAM1(NM_000201.2):c.1405A>G (p.K469E)
ISCN -
DB-ID ICAM1_000003 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.43895 View details
Owner VKGL-NL_Groningen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ICAM1 NM_000201.2 -/. - c.1405A>G r.(?) p.(Lys469Glu)
ICAM4 NM_001544.4 -/. - c.-2006A>G r.(?) p.(=)
ICAM5 NM_003259.3 -/. - c.-5037A>G r.(?) p.(=)