NM_017780.4(CHD7):c.1840G>A (p.Gly614Ser) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 9, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002412839.2
Allele description [Variation Report for NM_017780.4(CHD7):c.1840G>A (p.Gly614Ser)]
NM_017780.4(CHD7):c.1840G>A (p.Gly614Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
M130 of smooth muscle myosin phosphatase, partial [Sus scrofa]
M130 of smooth muscle myosin phosphatase, partial [Sus scrofa]gi|1695739|dbj|BAA13969.1|Protein
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Sus scrofa mRNA for M130 of smooth muscle myosin phosphatase, partial cds
Sus scrofa mRNA for M130 of smooth muscle myosin phosphatase, partial cdsgi|1695738|dbj|D89496.1|Nucleotide
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Last Updated: May 1, 2024