Variant position: 617 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 640 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 RSPNTGPYPSEQALPIPGTP PPNYDSLRLQPLDVIESDSEG
Chimpanzee RSPNTGPYPNEQALPIPGTP PPNYDSLRLQPLDVIESDSEG
Mouse CRPHGEVYPDQQTLPIPGTP PPNYDSLRLQPLDTMESDSEV
Rat CRPNAEVYPDQQTLPIPGTP PPNYDSLRLQPLDTMESDSEV
Bovine PGPDVEAYPHEQNPPIPGTP PPNYDSLRLQPLDVIESDSEG
Rabbit RSPDAEAYPDEQALPIPGTP PPNYDSLRLQPLDVVESDSEG
Sheep PGPDAGAYRREQNPPIPGTP PPNYDSLRLQPLDVIESDSEG
Xenopus laevis HVP----------VDIPGTP PPNYDSLRVNTAEPVSSDEEN
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.
Type Positions Description
1 – 640 Amiloride-sensitive sodium channel subunit beta
554 – 640 Cytoplasmic
590 – 640 Disordered
633 – 633 Phosphoserine
635 – 635 Phosphoserine
A family with Liddle's syndrome caused by a new missense mutation in the beta subunit of the epithelial sodium channel.
Inoue J.; Iwaoka T.; Tokunaga H.; Takamune K.; Naomi S.; Araki M.; Takahama K.; Yamaguchi K.; Tomita K.;
J. Clin. Endocrinol. Metab. 83:2210-2213(1998)
Cited for: VARIANT LIDLS1 SER-617;
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