Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001779.3
p.S170P
c.508T>C
Surrounding Variants
NM_001779.3
p.S170*
c.509C>G
NM_001779.3
p.S170*
c.509C>A
NM_001779.3
p.R168R
c.504T>C
NM_001779.3
p.R168C
c.502C>T
NM_001779.3
p.S172R
c.514A>C
NM_001779.3
p.S172R
c.516T>G
NM_001779.3
p.S172R
c.516T>A
NM_001779.3
p.C166*
c.498T>A
NM_001779.3
p.Y174fs
c.520_521fs
NM_001779.3
p.Q165*
c.493C>T
NM_001779.3
p.D160_M163del4
c.478_488del12
NM_001779.3
p.F175insFs
c.525dupT