NM_152721.6(DOK6):c.962A>C (p.Tyr321Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003209673.1
Allele description [Variation Report for NM_152721.6(DOK6):c.962A>C (p.Tyr321Ser)]
NM_152721.6(DOK6):c.962A>C (p.Tyr321Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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two-component response regulator ARR11 isoform X3 [Glycine max]
two-component response regulator ARR11 isoform X3 [Glycine max]gi|2027496269|ref|XP_040862884.1|Protein
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MYB-CC domain-containing transcription factor PHR21 isoform X1 [Glycine max]
MYB-CC domain-containing transcription factor PHR21 isoform X1 [Glycine max]gi|2027497167|ref|XP_040863041.1|Protein
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MYB-CC domain-containing transcription factor PHR14 isoform X3 [Glycine max]
MYB-CC domain-containing transcription factor PHR14 isoform X3 [Glycine max]gi|2027483590|ref|XP_040860723.1|Protein
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AL886253 XGC-egg Xenopus tropicalis cDNA clone TEgg031h13 5', mRNA sequence
AL886253 XGC-egg Xenopus tropicalis cDNA clone TEgg031h13 5', mRNA sequencegi|38677187|gnl|dbEST|20707362|emb| 253.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Apr 15, 2023