NM_000249.4(MLH1):c.214G>A (p.Asp72Asn) AND Colorectal cancer, hereditary nonpolyposis, type 2
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003473574.1
Allele description [Variation Report for NM_000249.4(MLH1):c.214G>A (p.Asp72Asn)]
NM_000249.4(MLH1):c.214G>A (p.Asp72Asn)
Condition(s)
- Name:
- Colorectal cancer, hereditary nonpolyposis, type 2 (LYNCH2)
- Synonyms:
- COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 2; Lynch syndrome II; MLH1-Related Lynch Syndrome; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0012249; MedGen: C1333991; Orphanet: 144; OMIM: 609310
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UDP-glycosyltransferase family 37 member C1 [Drosophila melanogaster]
UDP-glycosyltransferase family 37 member C1 [Drosophila melanogaster]gi|2329048337|ref|NP_525007.2|Protein
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Homo sapiens olfactory receptor, family 2, subfamily AT, member 4, mRNA (cDNA cl...
Homo sapiens olfactory receptor, family 2, subfamily AT, member 4, mRNA (cDNA clone MGC:168573 IMAGE:9020950), complete cdsgi|223462747|gb|BC136958.1|Nucleotide
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Last Updated: May 1, 2024