NM_172166.4(MSH5):c.2104C>T (p.His702Tyr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004283086.1
Allele description [Variation Report for NM_172166.4(MSH5):c.2104C>T (p.His702Tyr)]
NM_172166.4(MSH5):c.2104C>T (p.His702Tyr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens NIR1 mRNA, complete cds
Homo sapiens NIR1 mRNA, complete cdsgi|12667439|gb|AF334586.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024