Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 7:75933160 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041374 ; PhenCode IPNMDB_402 (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10823, 2010_April_001_036_HSPB1_602195_0005

This variation has 8 HGVS names - click the plus to show

7:g.75933160C>T
ENST00000248553.6:c.406C>T
ENSP00000248553.6:p.Arg136Trp
ENST00000447574.1:c.*570C>T
ENST00000429938.1:c.-99C>T
LRG_248:g.6286C>T
LRG_248t1.1:c.406C>T
LRG_248p1.1:p.Arg136Trp

Variation displays