NucleaRDB: Mutation data extracted by MuteXt

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This data was extracted from medline abstracts and full text papers (when available) in an automated manner.
This page litst all the point mutations extracted from the selected article.

Each point mutation is linked to the entry specific to the residue position and each sequence name to the list of mutations available for the corresponding protein.


Point mutations extracted from Melo KF et al., J Clin Endocrinol Metab 2003 [Medline]

MutationLocationGeneral numberingSwiss-Prot ID
S119XN-term-ANDR_HUMAN
L172XN-term-ANDR_HUMAN
L547FN-term-ANDR_HUMAN
T602PDNA_BINDD044ANDR_HUMAN
N705SLBD HELIX 3336ANDR_HUMAN
W741CLBD HELIX 5548ANDR_HUMAN
M742VLBD HELIX 5549ANDR_HUMAN
R752XLBD HELIX 5559ANDR_HUMAN
Y763CLoop 5-6-ANDR_HUMAN
L768PLoop 5-6-ANDR_HUMAN
L768VLoop 5-6-ANDR_HUMAN
R779WLoop 6-7-ANDR_HUMAN
M807VLBD HELIX 8854ANDR_HUMAN
R840SLBD HELIX 9952ANDR_HUMAN
R855CLBD HELIX 10-111039ANDR_HUMAN
R855HLBD HELIX 10-111039ANDR_HUMAN
I898FLBD HELIX 121251ANDR_HUMAN
I898TLBD HELIX 121251ANDR_HUMAN
P904HC-term-ANDR_HUMAN
P904RC-term-ANDR_HUMAN
P904SC-term-ANDR_HUMAN
P904VC-term-ANDR_HUMAN

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F.Horn (nucleardbcmbi.kun.nl), 21-Apr-2005