NM_001395207.1(SORBS2):c.674A>G (p.Asn225Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004336866.1
Allele description [Variation Report for NM_001395207.1(SORBS2):c.674A>G (p.Asn225Ser)]
NM_001395207.1(SORBS2):c.674A>G (p.Asn225Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens solute carrier family 12 member 6 (SLC12A6), transcript variant 2, ...
Homo sapiens solute carrier family 12 member 6 (SLC12A6), transcript variant 2, mRNAgi|110224450|ref|NM_005135.2|Nucleotide
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Taxonomy Links for Protein (Select 2023175277) (1)
Taxonomy
-
af85h09.s1 Soares_testis_NHT Homo sapiens cDNA clone 1048865 3', mRNA sequence
af85h09.s1 Soares_testis_NHT Homo sapiens cDNA clone 1048865 3', mRNA sequencegi|2837861|gnl|dbEST|1500205|gb|AA7 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Nov 24, 2024