Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 10:123040605 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM052824

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 24241

This variation has 11 HGVS names - click the plus to show

10:g.123040605C>T
ENST00000411816.1:c.460C>T
ENSP00000407744.1:p.Thr154Ile
ENST00000358776.6:c.443C>T
ENSP00000357873.3:p.Thr148Ile
ENST00000496730.2:n.402C>T
ENST00000368869.6:c.137C>T
ENSP00000357862.4:p.Thr46Ile
LRG_451:g.36693C>T
LRG_451t1:c.443C>T
LRG_451p1:p.Thr148Ile

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Variation displays