NM_006939.4(SOS2):c.3256C>T (p.Pro1086Ser) AND Noonan syndrome 9
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003755644.1
Allele description [Variation Report for NM_006939.4(SOS2):c.3256C>T (p.Pro1086Ser)]
NM_006939.4(SOS2):c.3256C>T (p.Pro1086Ser)
Condition(s)
-
RecName: Full=Transcription factor MYC2; Short=AtMYC2; AltName: Full=Basic helix...
RecName: Full=Transcription factor MYC2; Short=AtMYC2; AltName: Full=Basic helix-loop-helix protein 6; Short=AtbHLH6; Short=bHLH 6; AltName: Full=Protein JASMONATE INSENSITIVE 1; AltName: Full=R-homologous Arabidopsis protein 1; Short=RAP-1; AltName: Full=Transcription factor EN 38; AltName: Full=Z-box binding factor 1 protein; AltName: Full=bHLH transcription factor bHLH006; AltName: Full=rd22BP1gi|34222779|sp|Q39204.2|MYC2_ARATHProtein
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See more...Assertion and evidence details
Last Updated: Jul 15, 2024