NM_004278.4(PIGL):c.660+68C>A AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- May 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001609508.4
Allele description [Variation Report for NM_004278.4(PIGL):c.660+68C>A]
NM_004278.4(PIGL):c.660+68C>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens SNF8 subunit of ESCRT-II (SNF8), transcript variant 5, non-coding R...
Homo sapiens SNF8 subunit of ESCRT-II (SNF8), transcript variant 5, non-coding RNAgi|1701970469|ref|NR_133679.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024