Variant #0000577094 (NC_000023.10:g.68749609G>A, FAM155B(NM_015686.2):c.1229G>A)

Chromosome X
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.68749609G>A
DNA change (hg38) g.69529766G>A
Published as FAM155B(NM_015686.2):c.1229G>A (p.R410H)
ISCN -
DB-ID FAM155B_000018
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) 0.00019 View details
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM155B NM_015686.2 -?/. - c.1229G>A r.(?) p.(Arg410His)