Genomic variant #0000322201

Chromosome 11
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.44135818C>T
DNA change (hg38) -
Published as EXT2:NM_000401.3:c.809C>T, NM_001178083.1:c.710C>T, …
ISCN -
DB-ID EXT2_000126 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland; correct HGVS to be checked
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00223 View details
Owner VKGL-NL_Leiden




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
EXT2 NM_000401.3 -?/. - c.809C>T likely benign r.(?) p.(Ser270Leu)
EXT2 NM_207122.1 -?/. - c.710C>T likely benign r.(?) p.(Ser237Leu)