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NM_001371596.2(MFSD8):c.935T>C (p.Ile312Thr) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 24, 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:
RCV002517099.2

Allele description [Variation Report for NM_001371596.2(MFSD8):c.935T>C (p.Ile312Thr)]

NM_001371596.2(MFSD8):c.935T>C (p.Ile312Thr)

Gene:
MFSD8:major facilitator superfamily domain containing 8 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
4q28.2
Genomic location:
Preferred name:
NM_001371596.2(MFSD8):c.935T>C (p.Ile312Thr)
HGVS:
  • NC_000004.12:g.127930746A>G
  • NG_008657.1:g.40239T>C
  • NM_001363520.3:c.734T>C
  • NM_001363521.3:c.620T>C
  • NM_001371590.2:c.800T>C
  • NM_001371591.2:c.935T>C
  • NM_001371592.2:c.941T>C
  • NM_001371593.2:c.821T>C
  • NM_001371594.2:c.788T>C
  • NM_001371595.1:c.653T>C
  • NM_001371596.2:c.935T>CMANE SELECT
  • NM_001410765.1:c.485T>C
  • NM_001410766.1:c.821T>C
  • NM_152778.4:c.935T>C
  • NP_001350449.1:p.Ile245Thr
  • NP_001350449.1:p.Ile245Thr
  • NP_001350450.1:p.Ile207Thr
  • NP_001350450.1:p.Ile207Thr
  • NP_001358519.1:p.Ile267Thr
  • NP_001358519.1:p.Ile267Thr
  • NP_001358520.1:p.Ile312Thr
  • NP_001358520.1:p.Ile312Thr
  • NP_001358521.1:p.Ile314Thr
  • NP_001358521.1:p.Ile314Thr
  • NP_001358522.1:p.Ile274Thr
  • NP_001358522.1:p.Ile274Thr
  • NP_001358523.1:p.Ile263Thr
  • NP_001358523.1:p.Ile263Thr
  • NP_001358524.1:p.Ile218Thr
  • NP_001358525.1:p.Ile312Thr
  • NP_001397694.1:p.Ile162Thr
  • NP_001397695.1:p.Ile274Thr
  • NP_689991.1:p.Ile312Thr
  • LRG_833t1:c.935T>C
  • LRG_833t2:c.935T>C
  • LRG_833:g.40239T>C
  • LRG_833p1:p.Ile312Thr
  • LRG_833p2:p.Ile312Thr
  • NC_000004.11:g.128851901A>G
  • NM_001363520.2:c.734T>C
  • NM_001363521.2:c.620T>C
  • NM_001371590.1:c.800T>C
  • NM_001371591.1:c.935T>C
  • NM_001371592.1:c.941T>C
  • NM_001371593.1:c.821T>C
  • NM_001371594.1:c.788T>C
  • NM_152778.2:c.935T>C
Protein change:
I162T
Links:
dbSNP: rs556875684
NCBI 1000 Genomes Browser:
rs556875684
Molecular consequence:
  • NM_001363520.3:c.734T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001363521.3:c.620T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371590.2:c.800T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371591.2:c.935T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371592.2:c.941T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371593.2:c.821T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371594.2:c.788T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371595.1:c.653T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371596.2:c.935T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001410765.1:c.485T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001410766.1:c.821T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_152778.4:c.935T>C - missense variant - [Sequence Ontology: SO:0001583]
Functional consequence:
Unknown function

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV003633128Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)
Uncertain significance
(Jun 24, 2022)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV003633128.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The c.935T>C (p.I312T) alteration is located in exon 10 (coding exon 9) of the MFSD8 gene. This alteration results from a T to C substitution at nucleotide position 935, causing the isoleucine (I) at amino acid position 312 to be replaced by a threonine (T). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: May 1, 2024