Full database search - CCHMC Molecular Genetics Laboratory Mutation Database

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The variants below are all in the PSIP1 database, matching your query. All fields are shown, including patient and pathogenicity information. A '+' in the DNA change field indicates that more variants were found in this patient. Variants reported in a gene database other than PSIP1, are reported as the gene symbol with the number of reported variants between parenthesis.
Selecting and clicking a specific line will open a detailed view showing all details per patient.
At the bottom of this page a legend is provided with a short explanation of what each field contains.
For a more detailed description of each field, please see the PSIP1 full legend here.

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Path.

Technique

Template

DNA change

Protein

dbSNP ID

Race

Reference

Ethnic origin


?/?	SEQ	DNA	c.1312C>G + STK10 (1)	p.Gln438Glu	-	-	-	Unknown

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Sequence variations are described basically as recommended by the Ad-Hoc Committee for Mutation Nomenclature (AHCMN), with the recently suggested additions (den Dunnen JT and Antonarakis SE [2000], Hum.Mut. 15:7-12); for a summary see Nomenclature. Coding DNA Reference Sequence, with the first base of the Met-codon counted as position 1.
Path.: Variant pathogenicity, in the format Reported/Concluded; '+' indicating the variant is pathogenic, '+?' probably pathogenic, '-' no known pathogenicity, '-?' probably no pathogenicity, '?' effect unknown. Technique: Technique used to detect the variation. Template: Variant detected in DNA, RNA and/or Protein. DNA change: Variation at DNA-level to coding DNA Reference Sequence. ex: c.7C>T, c.-15T>A, c.77+1G>A, 78-1G>A, c.*2T>A Protein: Variation at protein level. dbSNP ID: rs# Race: Reference: Reference describing the variation, "Submitted:" indicating that the mutation was submitted directly to this database. Ethnic origin: Ethnic origin of patient

CCHMC Molecular Genetics Laboratory Mutation Database

PC4 and SFRS1 interacting protein 1 (PSIP1)