Genomic variant #0000331332

Chromosome 6
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.158579334G>A
DNA change (hg38) g.158158302G>A
Published as SERAC1(NM_032861.3):c.62C>T (p.P21L, p.(Pro21Leu))
ISCN -
DB-ID SERAC1_000032 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00323 View details
Owner VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERAC1 NM_032861.3 -?/. - c.62C>T r.(?) p.(Pro21Leu)