NM_017780.4(CHD7):c.1565G>T (p.Gly522Val) AND not specified
- Germline classification:
- Benign/Likely benign (4 submissions)
- Last evaluated:
- Apr 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000243125.22
Allele description [Variation Report for NM_017780.4(CHD7):c.1565G>T (p.Gly522Val)]
NM_017780.4(CHD7):c.1565G>T (p.Gly522Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
kdsA [Rickettsia conorii str. Malish 7]
kdsA [Rickettsia conorii str. Malish 7]Gene ID:928110Gene
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024