NM_001079802.2(FKTN):c.444C>T (p.Asp148=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 9, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002233016.1
Allele description [Variation Report for NM_001079802.2(FKTN):c.444C>T (p.Asp148=)]
NM_001079802.2(FKTN):c.444C>T (p.Asp148=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens DEAD-box helicase 49 (DDX49), transcript variant 1, mRNA
Homo sapiens DEAD-box helicase 49 (DDX49), transcript variant 1, mRNAgi|1519244084|ref|NM_019070.5|Nucleotide
-
Microbe sample from Paenibacillus sp. nov. IHBB 9951
Microbe sample from Paenibacillus sp. nov. IHBB 9951biosample
-
hypothetical protein [Sulfolobus sp. S-194]
hypothetical protein [Sulfolobus sp. S-194]gi|2752240076|ref|WP_353616886.1|Protein
-
IS6 family transposase [Sulfolobus sp. S-194]
IS6 family transposase [Sulfolobus sp. S-194]gi|2523706127|ref|WP_286189101.1|Protein
-
ACYP2 [Bos indicus]
ACYP2 [Bos indicus]Gene ID:109566075Gene
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Last Updated: Sep 29, 2024