NM_002016.2(FLG):c.4184T>C (p.Val1395Ala) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003365825.2
Allele description [Variation Report for NM_002016.2(FLG):c.4184T>C (p.Val1395Ala)]
NM_002016.2(FLG):c.4184T>C (p.Val1395Ala)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
HS3ST5 [Piliocolobus tephrosceles]
HS3ST5 [Piliocolobus tephrosceles]Gene ID:111547312Gene
-
PPP1R3D [Oenanthe melanoleuca]
PPP1R3D [Oenanthe melanoleuca]Gene ID:130261426Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024