Variant #0000289339 (NC_000019.9:g.10394725C>G, ICAM1(NM_000201.2):c.654C>G)

Chromosome 19
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.10394725C>G
DNA change (hg38) g.10284049C>G
Published as ICAM1(NM_000201.2):c.654C>G (p.P218=)
ISCN -
DB-ID ICAM1_000002
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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ICAM1 NM_000201.2 -?/. - c.654C>G r.(?) p.(Pro218=)
ICAM4 NM_001544.4 -?/. - c.-2964C>G r.(?) p.(=)