Variant #0000558781 (NC_000016.9:g.67976734G>A, LCAT(NM_000229.1):c.427+30C>T)

Chromosome 16
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.67976734G>A
DNA change (hg38) g.67942831G>A
Published as LCAT(NM_000229.1):c.427+30C>T
ISCN -
DB-ID LCAT_000155
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) 0.00192 View details
Owner VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LCAT NM_000229.1 -/. - c.427+30C>T r.(=) p.(=)
SLC12A4 NM_005072.4 -/. - c.*2009C>T r.(=) p.(=)