NM_001184.4(ATR):c.2776T>C (p.Phe926Leu) AND Seckel syndrome 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000264411.6
Allele description [Variation Report for NM_001184.4(ATR):c.2776T>C (p.Phe926Leu)]
NM_001184.4(ATR):c.2776T>C (p.Phe926Leu)
Condition(s)
-
Arabidopsis thaliana ubiquitin E2 variant 1D-4 (UEV1D-4), mRNA
Arabidopsis thaliana ubiquitin E2 variant 1D-4 (UEV1D-4), mRNAgi|1063716390|ref|NM_115116.4|Nucleotide
-
qq18b05.x1 Soares_NhHMPu_S1 Homo sapiens cDNA clone IMAGE:1932849 3', mRNA seque...
qq18b05.x1 Soares_NhHMPu_S1 Homo sapiens cDNA clone IMAGE:1932849 3', mRNA sequencegi|4070574|gnl|dbEST|2117757|gb|AI3 .1|Nucleotide
-
Stt3B [Vespa crabro]
Stt3B [Vespa crabro]Gene ID:124431040Gene
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Last Updated: Sep 29, 2024