NM_000168.6(GLI3):c.1800G>A (p.Thr600=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 16, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000975287.3
Allele description [Variation Report for NM_000168.6(GLI3):c.1800G>A (p.Thr600=)]
NM_000168.6(GLI3):c.1800G>A (p.Thr600=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
Homo sapiens placenta associated 8 (PLAC8), transcript variant 2, mRNA
Homo sapiens placenta associated 8 (PLAC8), transcript variant 2, mRNAgi|1677531156|ref|NM_016619.3|Nucleotide
-
A disintegrin and metalloproteinase with thrombospondin motifs 10 isoform X3 [Ho...
A disintegrin and metalloproteinase with thrombospondin motifs 10 isoform X3 [Homo sapiens]gi|2217323285|ref|XP_047295438.1|Protein
-
PREDICTED: Homo sapiens ADAM metallopeptidase with thrombospondin type 1 motif 1...
PREDICTED: Homo sapiens ADAM metallopeptidase with thrombospondin type 1 motif 10 (ADAMTS10), transcript variant X3, mRNAgi|2462567948|ref|XM_054322261.1|Nucleotide
-
equilibrative nucleoside transporter 2 isoform b [Homo sapiens]
equilibrative nucleoside transporter 2 isoform b [Homo sapiens]gi|664805964|ref|NP_001287798.1|Protein
-
equilibrative nucleoside transporter 2 isoform X3 [Homo sapiens]
equilibrative nucleoside transporter 2 isoform X3 [Homo sapiens]gi|2217282601|ref|XP_047282819.1|Protein
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Last Updated: Jul 29, 2023