NM_024680.4(E2F8):c.635A>G (p.Lys212Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004290464.1
Allele description [Variation Report for NM_024680.4(E2F8):c.635A>G (p.Lys212Arg)]
NM_024680.4(E2F8):c.635A>G (p.Lys212Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
voltage-gated hydrogen channel 1 isoform X2 [Homo sapiens]
voltage-gated hydrogen channel 1 isoform X2 [Homo sapiens]gi|2217291449|ref|XP_047285626.1|Protein
-
PREDICTED: Homo sapiens ATP binding cassette subfamily G member 4 (ABCG4), trans...
PREDICTED: Homo sapiens ATP binding cassette subfamily G member 4 (ABCG4), transcript variant X1, mRNAgi|2462526931|ref|XM_054369630.1|Nucleotide
-
Streptococcus pyogenes ABC020054353
Streptococcus pyogenes ABC020054353Group A StreptococcusBioProject
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Last Updated: Oct 8, 2024