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Mutations on the Protein: P69905 From Positions: 21 To 28

27
11
0
16




Swiss-Prot Polymorphism: VAR_002741
p.ALA22ASP
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002747
p.ALA27GLU
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002742
p.ALA22PRO
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_025387
p.ALA27VAL
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002748
p.GLU28ASP
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002744
p.GLU24GLY
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002749
p.GLU28GLY
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002745
p.GLU24LYS
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002750
p.GLU28VAL
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002743
p.GLY23ASP
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002746
p.TYR25HIS
N/A
N/A
N/A


OMIM Disease: 141800.0132
p.ALA26GLU
N/A
N/A
HEMOGLOBIN SHENYANG


OMIM Disease: 141800.0188
p.GLU23ASP
N/A
N/A
HEMOGLOBIN LISBON


OMIM Disease: 141800.0051
p.GLU27ASP
N/A
N/A
HEMOGLOBIN HEKINAN


OMIM Disease: 141800.0096
p.GLU23GLN
N/A
N/A
HEMOGLOBIN MEMPHIS


OMIM Disease: 141800.0124
p.GLU23GLY
N/A
N/A
HEMOGLOBIN REIMS


OMIM Disease: 141800.0037
p.GLU27GLY
N/A
N/A
HEMOGLOBIN G (FORT WORTH)||HEMOGLOBIN FORT WORTH


OMIM Disease: 141800.0016
p.GLU23LYS
N/A
N/A
HEMOGLOBIN CHAD


OMIM Disease: 141800.0134
p.GLU27LYS
N/A
N/A
HEMOGLOBIN SHUANGFENG


OMIM Disease: 141800.0035
p.GLU23VAL
N/A
N/A
HEMOGLOBIN G (AUDHALI)


OMIM Disease: 141800.0067
p.GLY22ASP
N/A
N/A
HEMOGLOBIN J (MEDELLIN)


OMIM Disease: 141800.0186
p.TYR24CYS
N/A
N/A
HEMOGLOBIN RAMONA


OMIM Disease: 141800.0091
p.TYR24HIS
N/A
N/A
HEMOGLOBIN LUXEMBOURG


OMIM Disease: 141850.0041
p.ALA26VAL
N/A
N/A
HEMOGLOBIN CAMPINAS


OMIM Disease: 141850.0063
p.GLU23TER
N/A
N/A
ALPHA-THALASSEMIA


OMIM Disease: 141850.0009
p.GLU27VAL
N/A
N/A
HEMOGLOBIN SPANISH TOWN


OMIM Disease: 141850.0064
p.GLY22GLY
N/A
N/A
ALPHA-PLUS-THALASSEMIA






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