Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 4:186196007 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041497

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_207352.3:c.332T>C, 15843

This variation has 3 HGVS names - click the plus to show

4:g.186196007T>C
ENST00000378802.4:c.332T>C
ENSP00000368079.4:p.Ile111Thr

Variation displays