NM_014638.4(PLCH2):c.1639T>C (p.Ser547Pro) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004513903.1
Allele description [Variation Report for NM_014638.4(PLCH2):c.1639T>C (p.Ser547Pro)]
NM_014638.4(PLCH2):c.1639T>C (p.Ser547Pro)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
MAG: hypothetical protein COV13_00705 [Candidatus Woesearchaeota archaeon CG10_b...
MAG: hypothetical protein COV13_00705 [Candidatus Woesearchaeota archaeon CG10_big_fil_rev_8_21_14_0_10_32_9]gi|1276411658|gb|PIN81611.1||gnl|WG F|COV13_00705Protein
-
unique_partial_genomes
unique_partial_genomesbiosample
-
BioSample links for Nucleotide (Select 931475144) (1)
BioSample
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Last Updated: May 7, 2024