NM_007313.3(ABL1):c.20A>G (p.Lys7Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 6, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002636938.9
Allele description [Variation Report for NM_007313.3(ABL1):c.20A>G (p.Lys7Arg)]
NM_007313.3(ABL1):c.20A>G (p.Lys7Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens coiled-coil domain containing 77 (CCDC77), transcript variant 2, mR...
Homo sapiens coiled-coil domain containing 77 (CCDC77), transcript variant 2, mRNAgi|1674986106|ref|NM_001130146.2|Nucleotide
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PREDICTED: Homo sapiens trafficking protein particle complex subunit 10 (TRAPPC1...
PREDICTED: Homo sapiens trafficking protein particle complex subunit 10 (TRAPPC10), transcript variant X19, mRNAgi|2217338175|ref|XM_011529727.3|Nucleotide
-
eukaryotic translation initiation factor 4 gamma 3 isoform X1 [Danio rerio]
eukaryotic translation initiation factor 4 gamma 3 isoform X1 [Danio rerio]gi|688577519|ref|XP_009304364.1|Protein
-
Homo sapiens cDNA: FLJ22669 fis, clone HSI08594
Homo sapiens cDNA: FLJ22669 fis, clone HSI08594gi|10439147|dbj|AK026322.1|Nucleotide
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Last Updated: Oct 8, 2024