Genomic variant #0000577788

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.92964837A>C
DNA change (hg38) -
Published as FAM133A(NM_001171109.1):c.419A>C (p.(Lys140Thr))
ISCN -
DB-ID FAM133A_000006
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     
FAM133A NM_173698.2 -?/. - c.419A>C likely benign r.(?) p.(Lys140Thr)