NM_018518.5(MCM10):c.1867A>G (p.Met623Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004285191.1
Allele description [Variation Report for NM_018518.5(MCM10):c.1867A>G (p.Met623Val)]
NM_018518.5(MCM10):c.1867A>G (p.Met623Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens consortin, connexin sorting protein (CNST), transcript v...
PREDICTED: Homo sapiens consortin, connexin sorting protein (CNST), transcript variant X4, mRNAgi|2217264552|ref|XM_047447903.1|Nucleotide
-
PREDICTED: Homo sapiens protein disulfide isomerase like, testis expressed (PDIL...
PREDICTED: Homo sapiens protein disulfide isomerase like, testis expressed (PDILT), transcript variant X3, mRNAgi|2462547949|ref|XM_054379808.1|Nucleotide
-
Amytornis textilis carteri voucher NMV<AUS>:HLW6602 NADH dehydrogenase subunit 2...
Amytornis textilis carteri voucher NMV<AUS>:HLW6602 NADH dehydrogenase subunit 2 (ND2) gene, partial cds; mitochondrialgi|543906145|gb|KF053523.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024