NM_024711.6(GIMAP6):c.199G>A (p.Glu67Lys) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 20, 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:: RCV004075749.1

Allele description [Variation Report for NM_024711.6(GIMAP6):c.199G>A (p.Glu67Lys)]

NM_024711.6(GIMAP6):c.199G>A (p.Glu67Lys)

Gene:

GIMAP6:GTPase, IMAP family member 6 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q36.1

Genomic location:

Preferred name:

NM_024711.6(GIMAP6):c.199G>A (p.Glu67Lys)

HGVS:

NC_000007.14:g.150628399C>T
NM_001244071.2:c.86-111G>A
NM_001244072.2:c.409G>A
NM_024711.6:c.199G>AMANE SELECT
NP_001231001.1:p.Glu137Lys
NP_078987.3:p.Glu67Lys
NC_000007.13:g.150325487C>T
NM_024711.5:c.199G>A

Protein change:

E137K

Molecular consequence:

NM_001244071.2:c.86-111G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001244072.2:c.409G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_024711.6:c.199G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Human sample from Homo sapiens
Human sample from Homo sapiens

biosample
Caenorhabditis elegans NR LBD domain-containing protein (nhr-21), mRNA
Caenorhabditis elegans NR LBD domain-containing protein (nhr-21), mRNA
gi|1845972396|ref|NM_001026930.4|

Nucleotide
Cichlasoma pearsei bio-material Chiapas microphthalmia-related transcription fac...
Cichlasoma pearsei bio-material Chiapas microphthalmia-related transcription factor b (Mitfb) gene, partial cds
gi|298353621|gb|GU946408.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003537471	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jul 20, 2021)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003537471

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jul 20, 2021)

germline

clinical testing

Citation Link

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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, SCV003537471.2

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

Description

The c.199G>A (p.E67K) alteration is located in exon 3 (coding exon 2) of the GIMAP6 gene. This alteration results from a G to A substitution at nucleotide position 199, causing the glutamic acid (E) at amino acid position 67 to be replaced by a lysine (K). 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 3, 2024

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