NM_173582.6(PGM2L1):c.111+146C>T AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- May 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001639667.4
Allele description [Variation Report for NM_173582.6(PGM2L1):c.111+146C>T]
NM_173582.6(PGM2L1):c.111+146C>T
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
rab-like protein 2A isoform X5 [Homo sapiens]
rab-like protein 2A isoform X5 [Homo sapiens]gi|2462569567|ref|XP_054196248.1|Protein
-
PREDICTED: Homo sapiens RAB, member of RAS oncogene family like 2A (RABL2A), tra...
PREDICTED: Homo sapiens RAB, member of RAS oncogene family like 2A (RABL2A), transcript variant X27, mRNAgi|2217325184|ref|XM_047443058.1|Nucleotide
-
rab-like protein 2A isoform 2 [Homo sapiens]
rab-like protein 2A isoform 2 [Homo sapiens]gi|807201143|ref|NP_001293088.1|Protein
-
PREDICTED: Homo sapiens RAB, member of RAS oncogene family like 2A (RABL2A), tra...
PREDICTED: Homo sapiens RAB, member of RAS oncogene family like 2A (RABL2A), transcript variant X18, mRNAgi|2462569574|ref|XM_054340277.1|Nucleotide
-
PREDICTED: Homo sapiens RAB, member of RAS oncogene family like 2A (RABL2A), tra...
PREDICTED: Homo sapiens RAB, member of RAS oncogene family like 2A (RABL2A), transcript variant X26, mRNAgi|2462569590|ref|XM_054340285.1|Nucleotide
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Last Updated: Sep 29, 2024