NM_001171.6(ABCC6):c.2959C>A (p.Arg987Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001531233.19
Allele description [Variation Report for NM_001171.6(ABCC6):c.2959C>A (p.Arg987Ser)]
NM_001171.6(ABCC6):c.2959C>A (p.Arg987Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
OMIM Links for Nucleotide (Select 1934804105) (4)
OMIM
-
ral GTPase-activating protein subunit alpha-2 isoform X4 [Homo sapiens]
ral GTPase-activating protein subunit alpha-2 isoform X4 [Homo sapiens]gi|2217335686|ref|XP_047296276.1|Protein
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024