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Mutations on the Protein: P69905 From Positions: 85 To 92

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19




Swiss-Prot Polymorphism: VAR_002810
p.ALA89SER
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002806
p.ASP86TYR
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002805
p.ASP86VAL
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002809
p.HIS88ARG
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002808
p.HIS88ASN
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002807
p.LEU87ARG
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_049272
p.LEU92PHE
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002812
p.LEU92PRO
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_002811
p.LYS91MET
N/A
N/A
N/A


OMIM Disease: 141800.0090
p.ALA88SER
N/A
N/A
HEMOGLOBIN LOIRE


OMIM Disease: 141800.0063
p.ARG92GLN
N/A
N/A
HEMOGLOBIN J (CAPE TOWN)


OMIM Disease: 141800.0018
p.ARG92LEU
N/A
N/A
HEMOGLOBIN CHESAPEAKE


OMIM Disease: 141800.0185
p.ARG92TRP
N/A
N/A
HEMOGLOBIN CEMENELUM


OMIM Disease: 141800.0057
p.HIS87ARG
N/A
N/A
HEMOGLOBIN IWATA


OMIM Disease: 141800.0215
p.HIS89ARG
N/A
N/A
HEMOGLOBIN TAMANO


OMIM Disease: 141800.0220
p.HIS87ASN
N/A
N/A
HEMOGLOBIN AUCKLAND


OMIM Disease: 141800.0212
p.HIS89GLN
N/A
N/A
HEMOGLOBIN BUFFALO


OMIM Disease: 141800.0172
p.HIS89LEU
N/A
N/A
HEMOGLOBIN LUTON


OMIM Disease: 141800.0214
p.HIS89PRO
N/A
N/A
HEMOGLOBIN TOKYO


OMIM Disease: 141800.0093
p.HIS87TYR
N/A
N/A
HEMOGLOBIN M (IWATE)||HEMOGLOBIN M (KANKAKEE);;||HEMOGLOBIN M (OLDENBURG);;||HEMOGLOBIN M (SENDAI)


OMIM Disease: 141800.0213
p.HIS89TYR
N/A
N/A
HEMOGLOBIN VILLEURBANNE


OMIM Disease: 141800.0101
p.LEU86ARG
N/A
N/A
HEMOGLOBIN MOABIT


OMIM Disease: 141800.0119
p.LEU91PRO
N/A
N/A
HEMOGLOBIN PORT PHILLIP


OMIM Disease: 141800.0014
p.LYS90ASN
N/A
N/A
HEMOGLOBIN BROUSSAIS||HEMOGLOBIN J (BROUSSAIS);;||HEMOGLOBIN TAGAWA I


OMIM Disease: 141800.0048
p.LYS90MET
N/A
N/A
HEMOGLOBIN HANDA||HEMOGLOBIN MUNAKATA


OMIM Disease: 141800.0071
p.LYS90THR
N/A
N/A
HEMOGLOBIN J (RAJAPPEN)


OMIM Disease: 141850.0016
p.ALA88VAL
N/A
N/A
HEMOGLOBIN COLUMBIA MISSOURI


OMIM Disease: 141850.0043
p.LYS90ARG
N/A
N/A
HEMOGLOBIN CLINICO-MADRID






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