Variant position: 419 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 615 The length of the canonical sequence.
Location on the sequence:
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human SQGTQSQGSALQDPECFAHL LRFYDGICKWEEGSPTPVLHV
Mouse AQGTQGQGSALQDPECFAHL LRFYDGICKWEEGSPTPVLHV
Rat AQGTQGQGSALQDPECFAHL LRFYDGICKWEEGSPTPVLHV
Bovine TQGTQSQGSALQDPECFAHL LRFYDGICKWEEGSPTPVLHV
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1.
Toledo R.A.; Lourenco D.M.; Coutinho F.L.; Quedas E.; Mackowiack I.; Machado M.C.; Montenegro F.; Cunha-Neto M.B.; Liberman B.; Pereira M.A.; Correa P.H.; Toledo S.P.;
Clin. Endocrinol. (Oxf.) 67:377-384(2007)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] (ISOFORM 2); VARIANTS MEN1 89-LEU--ALA-95 DEL; PHE-147; ARG-418; PRO-419 AND CYS-476; VARIANT ALA-546;
Identification of three novel menin mutations (c.741delGTCA, c.1348T>C, c.1785delA) in unrelated Italian families affected with multiple endocrine neoplasia type 1: additional information for mutational screening.
Asteria C.; Faglia G.; Roncoroni R.; Borretta G.; Ribotto P.; Beck-Peccoz P.;
Hum. Mutat. 17:237-237(2001)
Cited for: VARIANT MEN1 PRO-419;
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