NM_018834.6(MATR3):c.1130-14C>G AND Amyotrophic lateral sclerosis type 21
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003844704.1
Allele description [Variation Report for NM_018834.6(MATR3):c.1130-14C>G]
NM_018834.6(MATR3):c.1130-14C>G
Condition(s)
-
SNX18P25 sorting nexin 18 pseudogene 25 [Homo sapiens]
SNX18P25 sorting nexin 18 pseudogene 25 [Homo sapiens]Gene ID:100419005Gene
-
SNX18P25 AND (alive[prop]) (1)
Gene
-
PDZ and LIM domain protein 7 isoform 4 [Homo sapiens]
PDZ and LIM domain protein 7 isoform 4 [Homo sapiens]gi|47157328|ref|NP_998801.1|Protein
-
PREDICTED: Morus notabilis uncharacterized LOC21409753 (LOC21409753), mRNA
PREDICTED: Morus notabilis uncharacterized LOC21409753 (LOC21409753), mRNAgi|1350188291|ref|XM_010110629.2|Nucleotide
-
adenine nucleotide translocase lysine N-methyltransferase isoform 2 [Mus musculu...
adenine nucleotide translocase lysine N-methyltransferase isoform 2 [Mus musculus]gi|553726989|ref|NP_001272911.1|Protein
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See more...Assertion and evidence details
Last Updated: Mar 5, 2024