NM_007348.4(ATF6):c.1532A>G (p.Gln511Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001911114.6
Allele description [Variation Report for NM_007348.4(ATF6):c.1532A>G (p.Gln511Arg)]
NM_007348.4(ATF6):c.1532A>G (p.Gln511Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens leukocyte specific transcript 1 (LST1), transcript variant 5, mRNA
Homo sapiens leukocyte specific transcript 1 (LST1), transcript variant 5, mRNAgi|45580735|ref|NM_205840.1|Nucleotide
-
Homo sapiens leukocyte specific transcript 1 (LST1), mRNA
Homo sapiens leukocyte specific transcript 1 (LST1), mRNAgi|6005740|ref|NM_007161.1|Nucleotide
-
U exon, partial [Human adenovirus 2]
U exon, partial [Human adenovirus 2]gi|56160508|ref|AP_000189.1|Protein
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Last Updated: Sep 29, 2024