NM_000614.4(CNTF):c.565C>T (p.Arg189Cys) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003395810.8
Allele description
NM_000614.4(CNTF):c.565C>T (p.Arg189Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 2, ...
Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 2, mRNAgi|1889577743|ref|NM_134425.4|Nucleotide
-
Homo sapiens sulfate/anion transporter SAT-1 protein (SLC26A1) mRNA, complete cd...
Homo sapiens sulfate/anion transporter SAT-1 protein (SLC26A1) mRNA, complete cdsgi|10835917|gb|AF297659.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Aug 4, 2024