NM_018401.3(STK32B):c.1191C>G (p.Asp397Glu) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 16, 2021
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV004186775.1

Allele description [Variation Report for NM_018401.3(STK32B):c.1191C>G (p.Asp397Glu)]

NM_018401.3(STK32B):c.1191C>G (p.Asp397Glu)

Gene:

STK32B:serine/threonine kinase 32B [Gene - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

4p16.2

Genomic location:

Preferred name:

NM_018401.3(STK32B):c.1191C>G (p.Asp397Glu)

HGVS:

NC_000004.12:g.5499029C>G
NG_051593.1:g.452707C>G
NG_051593.2:g.484645C>G
NM_001306082.2:c.1050C>G
NM_001345969.2:c.1101C>G
NM_018401.3:c.1191C>GMANE SELECT
NP_001293011.1:p.Asp350Glu
NP_001332898.1:p.Asp367Glu
NP_060871.1:p.Asp397Glu
NC_000004.11:g.5500756C>G
NM_018401.1:c.1191C>G

Protein change:

D350E

Molecular consequence:

NM_001306082.2:c.1050C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001345969.2:c.1101C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_018401.3:c.1191C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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protein CIP2A isoform X2 [Homo sapiens]
protein CIP2A isoform X2 [Homo sapiens]
gi|2462591649|ref|XP_054203383.1|

Protein
Homo sapiens heterochromatin protein 1 binding protein 3 (HP1BP3), transcript va...
Homo sapiens heterochromatin protein 1 binding protein 3 (HP1BP3), transcript variant 16, mRNA
gi|2178610414|ref|NM_001399820.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003685493	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Sep 16, 2021)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003685493

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Sep 16, 2021)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV003685493.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The c.1191C>G (p.D397E) alteration is located in exon 12 (coding exon 12) of the STK32B gene. This alteration results from a C to G substitution at nucleotide position 1191, causing the aspartic acid (D) at amino acid position 397 to be replaced by a glutamic acid (E). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 10, 2024

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