NM_014975.3(MAST1):c.3602A>G (p.Asn1201Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004416573.1
Allele description [Variation Report for NM_014975.3(MAST1):c.3602A>G (p.Asn1201Ser)]
NM_014975.3(MAST1):c.3602A>G (p.Asn1201Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
JGI_CAAR467.rev NIH_XGC_tropLiv1 Xenopus tropicalis cDNA clone IMAGE:7733375 3',...
JGI_CAAR467.rev NIH_XGC_tropLiv1 Xenopus tropicalis cDNA clone IMAGE:7733375 3', mRNA sequencegi|58860954|gnl|dbEST|27727551|gb|D 18.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024