NM_000179.3(MSH6):c.1472T>C (p.Met491Thr) AND Lynch syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004007323.2
Allele description [Variation Report for NM_000179.3(MSH6):c.1472T>C (p.Met491Thr)]
NM_000179.3(MSH6):c.1472T>C (p.Met491Thr)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
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Variovorax paradoxus ZNC0006 L980_288, whole genome shotgun sequence
Variovorax paradoxus ZNC0006 L980_288, whole genome shotgun sequencegi|736492388|gb|JROV01000282.1||gnl JROV01|L980_288Nucleotide
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Variovorax paradoxus ZNC0006 L980_306, whole genome shotgun sequence
Variovorax paradoxus ZNC0006 L980_306, whole genome shotgun sequencegi|736492350|gb|JROV01000300.1||gnl JROV01|L980_306Nucleotide
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Variovorax paradoxus ZNC0006 L980_289, whole genome shotgun sequence
Variovorax paradoxus ZNC0006 L980_289, whole genome shotgun sequencegi|736492385|gb|JROV01000283.1||gnl JROV01|L980_289Nucleotide
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Variovorax paradoxus ZNC0006 L980_350, whole genome shotgun sequence
Variovorax paradoxus ZNC0006 L980_350, whole genome shotgun sequencegi|736492224|gb|JROV01000343.1||gnl JROV01|L980_350Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024