GRCh37/hg19 17p11.2(chr17:19247504-19395911)x3 AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 7, 2011
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000751954.2
Allele description
GRCh37/hg19 17p11.2(chr17:19247504-19395911)x3
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
Homo sapiens GRIP and coiled-coil domain containing 2 (GCC2), transcript variant...
Homo sapiens GRIP and coiled-coil domain containing 2 (GCC2), transcript variant 2, non-coding RNAgi|254039637|ref|NR_028063.1|Nucleotide
-
Nuclear receptor subfamily 1, group H, member 2 [Homo sapiens]
Nuclear receptor subfamily 1, group H, member 2 [Homo sapiens]gi|57169200|gb|AAH33500.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Mar 4, 2023