NM_000168.6(GLI3):c.501G>A (p.Thr167=) AND Greig cephalopolysyndactyly syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000367232.13
Allele description [Variation Report for NM_000168.6(GLI3):c.501G>A (p.Thr167=)]
NM_000168.6(GLI3):c.501G>A (p.Thr167=)
Condition(s)
-
PREDICTED: Homo sapiens Rho GTPase activating protein 28 (ARHGAP28), transcript ...
PREDICTED: Homo sapiens Rho GTPase activating protein 28 (ARHGAP28), transcript variant X4, mRNAgi|2217317635|ref|XM_047437796.1|Nucleotide
-
PREDICTED: Homo sapiens Rho GTPase activating protein 28 (ARHGAP28), transcript ...
PREDICTED: Homo sapiens Rho GTPase activating protein 28 (ARHGAP28), transcript variant X7, mRNAgi|2217317641|ref|XM_047437799.1|Nucleotide
-
poly [ADP-ribose] polymerase 2 isoform X2 [Homo sapiens]
poly [ADP-ribose] polymerase 2 isoform X2 [Homo sapiens]gi|1034585925|ref|XP_016876401.1|Protein
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Last Updated: Jul 23, 2024