NM_001164277.2(SLC37A4):c.357C>G (p.Pro119=) AND Glucose-6-phosphate transport defect

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Jan 22, 2023
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000667842.6

Allele description [Variation Report for NM_001164277.2(SLC37A4):c.357C>G (p.Pro119=)]

NM_001164277.2(SLC37A4):c.357C>G (p.Pro119=)

Gene:

SLC37A4:solute carrier family 37 member 4 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q23.3

Genomic location:

Preferred name:

NM_001164277.2(SLC37A4):c.357C>G (p.Pro119=)

HGVS:

NC_000011.10:g.119028218G>C
NG_013331.1:g.7689C>G
NM_001164277.2:c.357C>GMANE SELECT
NM_001164278.2:c.357C>G
NM_001164279.2:c.138C>G
NM_001164280.2:c.357C>G
NM_001467.6:c.357C>G
NP_001157749.1:p.Pro119=
NP_001157749.1:p.Pro119=
NP_001157750.1:p.Pro119=
NP_001157751.1:p.Pro46=
NP_001157752.1:p.Pro119=
NP_001458.1:p.Pro119=
LRG_187t1:c.357C>G
LRG_187:g.7689C>G
LRG_187p1:p.Pro119=
NC_000011.9:g.118898928G>C
NM_001164277.1:c.357C>G

Links:

dbSNP: rs782358834

NCBI 1000 Genomes Browser:

rs782358834

Molecular consequence:

NM_001164277.2:c.357C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001164278.2:c.357C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001164279.2:c.138C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001164280.2:c.357C>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001467.6:c.357C>G - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Glucose-6-phosphate transport defect (GSD1B)
Synonyms:: Glycogen storage disease type 1B; GSD Ib
Identifiers:: MONDO: MONDO:0009288; MedGen: C0268146; Orphanet: 364; Orphanet: 79259; OMIM: 232220

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
SCV000792351	Counsyl	criteria provided, single submitter (Counsyl Autosomal Recessive and X-Linked Classification Criteria (2018))	Likely benign (Jun 14, 2017)	unknown	clinical testing	Citation Link,
SCV002450253	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Jan 22, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000792351

Counsyl

criteria provided, single submitter

(Counsyl Autosomal Recessive and X-Linked Classification Criteria (2018))

Likely benign
(Jun 14, 2017)

unknown

clinical testing

Citation Link,

SCV002450253

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Jan 22, 2023)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

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
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240-242.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Counsyl, SCV000792351.1

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

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

From Invitae, SCV002450253.3

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

#	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: Apr 15, 2024

ClinVar

Relating variation to medicine