NM_020848.4(JCAD):c.1451C>T (p.Ser484Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004635743.1
Allele description [Variation Report for NM_020848.4(JCAD):c.1451C>T (p.Ser484Leu)]
NM_020848.4(JCAD):c.1451C>T (p.Ser484Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens full length insert cDNA YQ04C07
Homo sapiens full length insert cDNA YQ04C07gi|3377609|gb|AF075068.1|HUMYQ04C07Nucleotide
-
LOC111776202 [Equus caballus]
LOC111776202 [Equus caballus]Gene ID:111776202Gene
-
OR7A221P [Equus caballus]
OR7A221P [Equus caballus]Gene ID:119645827Gene
-
TRNAI-UAU [Equus caballus]
TRNAI-UAU [Equus caballus]Gene ID:111768269Gene
-
LOC111776199 [Equus caballus]
LOC111776199 [Equus caballus]Gene ID:111776199Gene
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024