[Term]
id: PR:000044559
name: presenilin-1 sequence variant S169del (human)
def: "A presenilin-1 sequence variant (human) that has a single-residue deletion at the position equivalent to Ser-169 of the amino acid sequence represented by UniProtKB:P49768-1. Example: UniProtKB:P49768-1, 1-168, 170-467." [PRO:DAN, Alzforum:KD]
comment: Category=organism-sequence. Requested by=Alzforum.
synonym: "hPSEN1/var:S169del" EXACT PRO-short-label [PRO:DAN]
synonym: "UniProtKB:P49768, 1-168, 171-467" EXACT PRO-proteoform-std [PRO:DAN]
synonym: "UniProtKB:P49768-1, 1-168, 171-467" NARROW PRO-proteoform-std [PRO:DAN]
xref: Alzforum_mut:psen1-s169del-%CE%B4s169
is_a: PR:000036285 ! presenilin-1 sequence variant (human)
relationship: only_in_taxon NCBITaxon:9606 ! Homo sapiens