NM_015702.3(MMADHC):c.-53+18C>T AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 28, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000434153.2
Allele description [Variation Report for NM_015702.3(MMADHC):c.-53+18C>T]
NM_015702.3(MMADHC):c.-53+18C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens eukaryotic translation initiation factor 3 subunit C (EIF3C), trans...
Homo sapiens eukaryotic translation initiation factor 3 subunit C (EIF3C), transcript variant 2, mRNAgi|557128985|ref|NM_001037808.2|Nucleotide
-
Component(Core) Links for Nucleotide (Select 163954925) (9)
Nucleotide
-
Gene neighbors for Gene (Select 135229097) (0)
Gene
-
Gene Links for Nucleotide (Select 163954925) (8)
Gene
-
Fungal sp. PTFL004 internal transcribed spacer 1, partial sequence; 5.8S ribosom...
Fungal sp. PTFL004 internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequencegi|574961222|gb|KF911105.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023