NM_000230.3(LEP):c.21C>T (p.Cys7=) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (3 submissions)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000733683.21
Allele description [Variation Report for NM_000230.3(LEP):c.21C>T (p.Cys7=)]
NM_000230.3(LEP):c.21C>T (p.Cys7=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens MUC1 isoform M1 (MUC1) mRNA, complete cds
Homo sapiens MUC1 isoform M1 (MUC1) mRNA, complete cdsgi|151347330|gb|EF670706.1|Nucleotide
-
cytochrome oxidase subunit II, partial (mitochondrion) [Apis mellifera mellifera...
cytochrome oxidase subunit II, partial (mitochondrion) [Apis mellifera mellifera]gi|1390049687|gb|AWK84786.1|Protein
-
SAMD00565434 (1)
SRA
-
Homo sapiens MUC1 isoform M2 (MUC1) mRNA, complete cds
Homo sapiens MUC1 isoform M2 (MUC1) mRNA, complete cdsgi|151347332|gb|EF670707.1|Nucleotide
-
basic immunoglobulin-like variable motif-containing protein isoform X1 [Mus musc...
basic immunoglobulin-like variable motif-containing protein isoform X1 [Mus musculus]gi|1907069028|ref|XP_006496061.3|Protein
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See more...Assertion and evidence details
Last Updated: Oct 20, 2024