NM_001099646.3(SLC47A2):c.1199A>C (p.Lys400Thr) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 19, 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:: RCV004148466.1

Allele description [Variation Report for NM_001099646.3(SLC47A2):c.1199A>C (p.Lys400Thr)]

NM_001099646.3(SLC47A2):c.1199A>C (p.Lys400Thr)

Gene:

SLC47A2:solute carrier family 47 member 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17p11.2

Genomic location:

Preferred name:

NM_001099646.3(SLC47A2):c.1199A>C (p.Lys400Thr)

HGVS:

NC_000017.11:g.19681636T>G
NG_052805.1:g.42344A>C
NM_001099646.3:c.1199A>CMANE SELECT
NM_001256663.3:c.1241A>C
NM_152908.5:c.1307A>C
NP_001093116.1:p.Lys400Thr
NP_001243592.1:p.Lys414Thr
NP_690872.2:p.Lys436Thr
NC_000017.10:g.19584949T>G
NM_152908.3:c.1307A>C
NR_135624.2:n.1869A>C
NR_135625.3:n.1306A>C

Protein change:

K400T

Molecular consequence:

NM_001099646.3:c.1199A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001256663.3:c.1241A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_152908.5:c.1307A>C - missense variant - [Sequence Ontology: SO:0001583]
NR_135624.2:n.1869A>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_135625.3:n.1306A>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003633029	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jul 19, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003633029

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jul 19, 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, SCV003633029.2

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

Description

The c.1307A>C (p.K436T) alteration is located in exon 14 (coding exon 14) of the SLC47A2 gene. This alteration results from a A to C substitution at nucleotide position 1307, causing the lysine (K) at amino acid position 436 to be replaced by a threonine (T). 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 24, 2024

ClinVar

Relating variation to medicine