NM_138927.4(SON):c.5964T>C (p.Pro1988=) AND not provided
- Germline classification:
- Benign/Likely benign (4 submissions)
- Last evaluated:
- Jan 17, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000913277.18
Allele description [Variation Report for NM_138927.4(SON):c.5964T>C (p.Pro1988=)]
NM_138927.4(SON):c.5964T>C (p.Pro1988=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
wb43d10.x1 NCI_CGAP_GC6 Homo sapiens cDNA clone IMAGE:2308435 3' similar to TR:O...
wb43d10.x1 NCI_CGAP_GC6 Homo sapiens cDNA clone IMAGE:2308435 3' similar to TR:O60875 O60875 APOPTOSIS SPECIFIC PROTEIN, mRNA sequencegi|4737119|gnl|dbEST|2481784|gb|AI6 .1|Nucleotide
-
MHC class II antigen, partial [Homo sapiens]
MHC class II antigen, partial [Homo sapiens]gi|5381295|gb|AAD42928.1|Protein
-
SULZ_RS05455 [Saccharolobus solfataricus]
SULZ_RS05455 [Saccharolobus solfataricus]Gene ID:44129008Gene
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See more...Assertion and evidence details
Last Updated: Aug 4, 2024