GRCh37/hg19 5q15-22.3(chr5:93650000-114969108) AND not specified
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Mar 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002053511.3
Allele description [Variation Report for GRCh37/hg19 5q15-22.3(chr5:93650000-114969108)]
GRCh37/hg19 5q15-22.3(chr5:93650000-114969108)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens EMI domain containing 1 (EMID1), transcript variant 2, mRNA
Homo sapiens EMI domain containing 1 (EMID1), transcript variant 2, mRNAgi|1676439650|ref|NM_001267895.2|Nucleotide
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Chromosome neighbors for GEO Profiles (Select 69899664) (20)
GEO Profiles
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Chromosome neighbors for GEO Profiles (Select 69892951) (20)
GEO Profiles
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CYP2B6 cytochrome P450 family 2 subfamily B member 6 [Homo sapiens]
CYP2B6 cytochrome P450 family 2 subfamily B member 6 [Homo sapiens]Gene ID:1555Gene
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Gene Links for GEO Profiles (Select 69884828) (1)
Gene
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Last Updated: Oct 14, 2023