NM_006218.4(PIK3CA):c.288A>G (p.Gln96=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002437889.2
Allele description [Variation Report for NM_006218.4(PIK3CA):c.288A>G (p.Gln96=)]
NM_006218.4(PIK3CA):c.288A>G (p.Gln96=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
tt26g04.x1 NCI_CGAP_GC6 Homo sapiens cDNA clone IMAGE:2241942 3', mRNA sequence
tt26g04.x1 NCI_CGAP_GC6 Homo sapiens cDNA clone IMAGE:2241942 3', mRNA sequencegi|4690182|gnl|dbEST|2456753|gb|AI6 .1|Nucleotide
-
602034235F2 NCI_CGAP_Brn64 Homo sapiens cDNA clone IMAGE:4182153 5', mRNA sequen...
602034235F2 NCI_CGAP_Brn64 Homo sapiens cDNA clone IMAGE:4182153 5', mRNA sequencegi|11284963|gnl|dbEST|6785588|gb|BF 0.1|Nucleotide
-
Microbe sample from Verrucomicrobiales bacterium VVV1
Microbe sample from Verrucomicrobiales bacterium VVV1biosample
-
MAG: Flavobacterium sp. BFFFF2, whole genome shotgun sequencing project
MAG: Flavobacterium sp. BFFFF2, whole genome shotgun sequencing projectgi|1232152876|gb|NKJD00000000.1|NKJ 0000Nucleotide
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Last Updated: May 1, 2024