Sequence information
Variant position: 1624 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 2725 The length of the canonical sequence.
Location on the sequence:
PDMSGRYTITIKYGGDEIPY
S PFRIHALPTGDASKCLVTVS
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 PDMSGRYTITIKYGGDEIPYS PFRIHALPTGDASKCLVTVS
Mouse PDMSGRYTITIKYGGDEIPYS PFRIHALPTGDASKCLVTVS
Rat PDMSGRYTITIKYGGDEIPYS PFRIHALPTGDASKCLVTVS
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.
Literature citations
Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy.
Brodehl A.; Ferrier R.A.; Hamilton S.J.; Greenway S.C.; Brundler M.A.; Yu W.; Gibson W.T.; McKinnon M.L.; McGillivray B.; Alvarez N.; Giuffre M.; Schwartzentruber J.; Gerull B.;
Hum. Mutat. 37:269-279(2016)
Cited for: INVOLVEMENT IN RCM5; VARIANTS RCM5 LEU-1624 AND PHE-2160; CHARACTERIZATION OF VARIANT RCM5 LEU-1624;
Disclaimer:
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.