NM_001374828.1(ARID1B):c.3089+4_3089+5insCTAC AND ARID1B-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004543955.1
Allele description
NM_001374828.1(ARID1B):c.3089+4_3089+5insCTAC
Condition(s)
- Name:
- ARID1B-related disorder
- Identifiers:
-
Homo sapiens CD2 molecule (CD2), transcript variant 2, mRNA
Homo sapiens CD2 molecule (CD2), transcript variant 2, mRNAgi|1519314580|ref|NM_001767.5|Nucleotide
-
Profile neighbors for GEO Profiles (Select 131940335) (65)
GEO Profiles
-
EFCAB11 EF-hand calcium binding domain 11 [Homo sapiens]
EFCAB11 EF-hand calcium binding domain 11 [Homo sapiens]Gene ID:90141Gene
-
Gene Links for GEO Profiles (Select 131947115) (1)
Gene
-
SLC1A2 solute carrier family 1 member 2 [Homo sapiens]
SLC1A2 solute carrier family 1 member 2 [Homo sapiens]Gene ID:6506Gene
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Last Updated: Sep 29, 2024