NM_000240.4(MAOA):c.891G>T (p.Arg297=) AND not specified
Clinical significance:Benign (Last evaluated: Jul 16, 2015)
Review status:
- Based on:
- 2 submissions [Details]
- Record status:
- current
- Accession:
- RCV000078415.16
Allele description [Variation Report for NM_000240.4(MAOA):c.891G>T (p.Arg297=)]
NM_000240.4(MAOA):c.891G>T (p.Arg297=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Moloney murine leukemia virus, complete genome
Moloney murine leukemia virus, complete genomegi|331934|gb|J02255.1|MLMCGNucleotide
-
Xenotropic MuLV-related virus VP62, complete genome
Xenotropic MuLV-related virus VP62, complete genomegi|121104176|gb|EF185282.1|Nucleotide
-
Friend murine leukemia virus FB29 complete genome
Friend murine leukemia virus FB29 complete genomegi|61547|emb|Z11128.1|Nucleotide
-
mlv-related virus cfs (15)
Nucleotide
-
AIFM1 apoptosis inducing factor mitochondria associated 1 [Homo sapiens]
AIFM1 apoptosis inducing factor mitochondria associated 1 [Homo sapiens]Gene ID:9131Gene
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See more...Assertion and evidence details
Last Updated: Aug 23, 2022