NM_001378189.1(CFAP57):c.-56T>C AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004106679.1
Allele description [Variation Report for NM_001378189.1(CFAP57):c.-56T>C]
NM_001378189.1(CFAP57):c.-56T>C
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens cDNA FLJ36681 fis, clone UTERU2006547
Homo sapiens cDNA FLJ36681 fis, clone UTERU2006547gi|21752972|dbj|AK094000.1|Nucleotide
-
PMC Links for GEO Profiles (Select 98547295) (2)
PMC
-
hypothetical protein J1G47_11555 (plasmid) [Glaesserella parasuis]
hypothetical protein J1G47_11555 (plasmid) [Glaesserella parasuis]gi|2006089171|gnl|PRJNA707125|J1G47 5|gb|QSX11817.1|Protein
-
POFUT1 [Pan paniscus]
POFUT1 [Pan paniscus]Gene ID:100974304Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024