NM_015094.3(HIC2):c.1229C>T (p.Ala410Val) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 3, 2022
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:: RCV004163128.1

Allele description [Variation Report for NM_015094.3(HIC2):c.1229C>T (p.Ala410Val)]

NM_015094.3(HIC2):c.1229C>T (p.Ala410Val)

Gene:

HIC2:HIC ZBTB transcriptional repressor 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

22q11.21

Genomic location:

Preferred name:

NM_015094.3(HIC2):c.1229C>T (p.Ala410Val)

HGVS:

NC_000022.11:g.21446124C>T
NM_015094.3:c.1229C>TMANE SELECT
NP_055909.2:p.Ala410Val
NC_000022.10:g.21800413C>T
NM_015094.2:c.1229C>T

Protein change:

A410V

Molecular consequence:

NM_015094.3:c.1229C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

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Mus musculus adult male cerebellum cDNA, RIKEN full-length enriched library, clo...
Mus musculus adult male cerebellum cDNA, RIKEN full-length enriched library, clone:1500035D08 product:vesicle-associated membrane protein 1, full insert sequence
gi|12858677|dbj|AK018783.1|

Nucleotide
Mus musculus 12 days embryo head cDNA, RIKEN full-length enriched library, clone...
Mus musculus 12 days embryo head cDNA, RIKEN full-length enriched library, clone:3010005E14 product:vesicle-associated membrane protein 1, full insert sequence
gi|12851437|dbj|AK013893.1|

Nucleotide
RecName: Full=Glycerol kinase; Short=Glycerokinase; AltName: Full=ATP:glycerol 3...
RecName: Full=Glycerol kinase; Short=Glycerokinase; AltName: Full=ATP:glycerol 3-phosphotransferase
gi|205830912|sp|Q64516.2|GLPK_MOUSE

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003650710	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Oct 3, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003650710

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Oct 3, 2022)

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, SCV003650710.2

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

Description

The c.1229C>T (p.A410V) alteration is located in exon 2 (coding exon 2) of the HIC2 gene. This alteration results from a C to T substitution at nucleotide position 1229, causing the alanine (A) at amino acid position 410 to be replaced by a valine (V). 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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