GRCh37/hg19 4q28.1-35.1(chr4:124873497-185278662)x3 AND not provided
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Mar 14, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000849686.2
Allele description [Variation Report for GRCh37/hg19 4q28.1-35.1(chr4:124873497-185278662)x3]
GRCh37/hg19 4q28.1-35.1(chr4:124873497-185278662)x3
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PREDICTED: Homo sapiens TBC1 domain family member 12 (TBC1D12), transcript varia...
PREDICTED: Homo sapiens TBC1 domain family member 12 (TBC1D12), transcript variant X4, misc_RNAgi|2462518116|ref|XR_008488185.1|Nucleotide
-
H.sapiens mRNA for prolactin-inducible protein
H.sapiens mRNA for prolactin-inducible proteingi|2292895|emb|Y10179.1|Nucleotide
-
TBC1 domain family member 12 [Homo sapiens]
TBC1 domain family member 12 [Homo sapiens]gi|148806902|ref|NP_056003.1|Protein
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Last Updated: Sep 1, 2024