Genomic variant #0000624693

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.68749466G>C
DNA change (hg38) -
Published as FAM155B(NM_015686.2):c.1086G>C (p.Q362H)
ISCN -
DB-ID FAM155B_000022
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) Variant not found in online data sets
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
FAM155B NM_015686.2 ?/. - c.1086G>C VUS r.(?) p.(Gln362His)