NM_001287.6(CLCN7):c.394C>T (p.Leu132Phe) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003016994.3
Allele description [Variation Report for NM_001287.6(CLCN7):c.394C>T (p.Leu132Phe)]
NM_001287.6(CLCN7):c.394C>T (p.Leu132Phe)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Human DNA sequence from clone RP11-349N19 on chromosome X, complete sequence
Human DNA sequence from clone RP11-349N19 on chromosome X, complete sequencegi|15384946|emb|AL590139.11|Nucleotide
-
Human DNA sequence from clone RP5-1171F9 on chromosome Xq23-25, complete sequenc...
Human DNA sequence from clone RP5-1171F9 on chromosome Xq23-25, complete sequencegi|10045418|emb|AL356213.10|Nucleotide
-
SRP100110 (172)
SRA
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024