NM_000142.5(FGFR3):c.1619A>G (p.Asn540Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 25, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000623459.2
Allele description [Variation Report for NM_000142.5(FGFR3):c.1619A>G (p.Asn540Ser)]
NM_000142.5(FGFR3):c.1619A>G (p.Asn540Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens cDNA FLJ13024 fis, clone NT2RP3000865
Homo sapiens cDNA FLJ13024 fis, clone NT2RP3000865gi|10434843|dbj|AK023086.1|Nucleotide
-
UNVERIFIED: Isotomurus palustris isolate OG6076 succinate dehydrogenase mRNA, co...
UNVERIFIED: Isotomurus palustris isolate OG6076 succinate dehydrogenase mRNA, complete cdsgi|1584436917|gb|MH799995.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 26, 2024