20-46724875-C-CGGATGGATGGAT

Position:

• chr20-46724875-C-CGGATGGATGGAT

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP6_Moderate BA1

The NM_030777.4(SLC2A10):​c.5-147_5-136dupATGGATGGATGG variant causes a intron change involving the alteration of a non-conserved nucleotide. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.11 (2195 hom., cov: 0)
• Consequence: SLC2A10 NM_030777.4 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 0.234

Genes affected

SLC2A10 (HGNC:13444): (solute carrier family 2 member 10) This gene encodes a member of the class III facilitative glucose transporter family. The encoded protein plays a role in regulation of glucose homeostasis. Mutations in this gene have been associated with arterial tortuosity syndrome.[provided by RefSeq, Dec 2009]

ACMG classification

Verdict is Benign. Variant got -10 ACMG points.

• BP6: Variant 20-46724875-C-CGGATGGATGGAT is Benign according to our data. Variant chr20-46724875-C-CGGATGGATGGAT is described in ClinVar as [Benign]. Clinvar id is 1237574.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.309 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SLC2A10	NM_030777.4	c.5-147_5-136dupATGGATGGATGG		intron_variant		ENST00000359271.4	NP_110404.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SLC2A10	ENST00000359271.4	c.5-166_5-165insGGATGGATGGAT		intron_variant		1	NM_030777.4	ENSP00000352216.2
SLC2A10	ENST00000611837.1	n.157-166_157-165insGGATGGATGGAT		intron_variant		2

Frequencies

GnomAD3 genomes AF: 0.112 AC: 15622 AN: 139580 Hom.: 2187 Cov.: 0

Gnomad AFR AF: 0.314

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.143

Gnomad ASJ AF: 0.0266

Gnomad EAS AF: 0.0410

Gnomad SAS AF: 0.0286

Gnomad FIN AF: 0.0367

Gnomad MID AF: 0.0655

Gnomad NFE AF: 0.0204

Gnomad OTH AF: 0.0929

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.112 AC: 15648 AN: 139694 Hom.: 2195 Cov.: 0 AF XY: 0.113 AC XY: 7676 AN XY: 67732

Gnomad4 AFR AF: 0.313

Gnomad4 AMR AF: 0.144

Gnomad4 ASJ AF: 0.0266

Gnomad4 EAS AF: 0.0409

Gnomad4 SAS AF: 0.0282

Gnomad4 FIN AF: 0.0367

Gnomad4 NFE AF: 0.0204

Gnomad4 OTH AF: 0.0925

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Nov 14, 2019

- -

Computational scores

Source: dbNSFP v4.3

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs3092014; hg19: chr20-45353514;