11-66713635-G-A

Variant names:

Variant summary

Our verdict is Benign. The variant received -14 ACMG points: 0P and 14B. BP4_StrongBP6_Very_StrongBP7BS2_Supporting

The NM_006946.4(SPTBN2):c.768C>T(p.Pro256Pro) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000165 in 1,613,228 control chromosomes in the GnomAD database, including 2 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).

Frequency

Genomes: 𝑓 0.00018 ( 0 hom., cov: 31)

Exomes 𝑓: 0.00016 ( 2 hom. )

Consequence

SPTBN2
NM_006946.4 synonymous

Scores

Clinical Significance

Benign/Likely benign criteria provided, multiple submitters, no conflicts B:3

Conservation

PhyloP100: -3.45

Publications

0 publications found

Variant links:

Genes affected

SPTBN2 (HGNC:11276): (spectrin beta, non-erythrocytic 2) Spectrins are principle components of a cell's membrane-cytoskeleton and are composed of two alpha and two beta spectrin subunits. The protein encoded by this gene (SPTBN2), is called spectrin beta non-erythrocytic 2 or beta-III spectrin. It is related to, but distinct from, the beta-II spectrin gene which is also known as spectrin beta non-erythrocytic 1 (SPTBN1). SPTBN2 regulates the glutamate signaling pathway by stabilizing the glutamate transporter EAAT4 at the surface of the plasma membrane. Mutations in this gene cause a form of spinocerebellar ataxia, SCA5, that is characterized by neurodegeneration, progressive locomotor incoordination, dysarthria, and uncoordinated eye movements. [provided by RefSeq, Dec 2009]

SPTBN2 Gene-Disease associations (from GenCC):

autosomal recessive spinocerebellar ataxia 14
Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: PanelApp Australia, Labcorp Genetics (formerly Invitae), G2P, Orphanet
spinocerebellar ataxia type 5
Inheritance: AD Classification: STRONG, SUPPORTIVE Submitted by: Orphanet, Labcorp Genetics (formerly Invitae), Illumina, G2P

SPTBN2 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -14 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.85).

BP6

Variant 11-66713635-G-A is Benign according to our data. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr11-66713635-G-A is described in CliVar as Benign/Likely_benign. Clinvar id is 586492.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BP7

Synonymous conserved (PhyloP=-3.45 with no splicing effect.

BS2

High Homozygotes in GnomAdExome4 at 2 AD,AR geneVariant has number of homozygotes lower than other variant known as pathogenic in the gene, so the strength is limited to Supporting.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SPTBN2	NM_006946.4 link	c.768C>T	p.Pro256Pro	synonymous_variant	Exon 8 of 38	ENST00000533211.6	NP_008877.2	O15020-1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SPTBN2	ENST00000533211.6 link	c.768C>T	p.Pro256Pro	synonymous_variant	Exon 8 of 38	5	NM_006946.4	ENSP00000432568.1		O15020-1

Frequencies

GnomAD3 genomes

AF:

0.000178

AC:

AN:

152050

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.000169

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.00

Gnomad ASJ

AF:

0.00259

Gnomad EAS

AF:

0.000192

Gnomad SAS

AF:

0.00

Gnomad FIN

AF:

0.00

Gnomad MID

AF:

0.00

Gnomad NFE

AF:

0.000132

Gnomad OTH

AF:

0.000478

GnomAD2 exomes

AF:

0.000255

AC:

AN:

251316

AF XY:

0.000258

show subpopulations

Gnomad AFR exome

AF:

0.0000615

Gnomad AMR exome

AF:

0.0000867

Gnomad ASJ exome

AF:

0.00427

Gnomad EAS exome

AF:

0.000272

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.000105

Gnomad OTH exome

AF:

0.00

GnomAD4 exome

AF:

0.000164

AC:

239

AN:

1461060

Hom.:

Cov.:

AF XY:

0.000166

AC XY:

121

AN XY:

726916

show subpopulations

African (AFR)

AF:

0.0000598

AC:

AN:

33464

American (AMR)

AF:

0.000134

AC:

AN:

44724

Ashkenazi Jewish (ASJ)

AF:

0.00386

AC:

101

AN:

26134

East Asian (EAS)

AF:

0.000101

AC:

AN:

39698

South Asian (SAS)

AF:

0.00

AC:

AN:

86238

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53162

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5734

European-Non Finnish (NFE)

AF:

0.0000990

AC:

110

AN:

1111526

Other (OTH)

AF:

0.000265

AC:

AN:

60380

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.476

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

AF:

0.000177

AC:

AN:

152168

Hom.:

Cov.:

AF XY:

0.000148

AC XY:

AN XY:

74398

show subpopulations

African (AFR)

AF:

0.000169

AC:

AN:

41482

American (AMR)

AF:

0.00

AC:

AN:

15274

Ashkenazi Jewish (ASJ)

AF:

0.00259

AC:

AN:

3470

East Asian (EAS)

AF:

0.000193

AC:

AN:

5186

South Asian (SAS)

AF:

0.00

AC:

AN:

4826

European-Finnish (FIN)

AF:

0.00

AC:

AN:

10588

Middle Eastern (MID)

AF:

0.00

AC:

AN:

294

European-Non Finnish (NFE)

AF:

0.000132

AC:

AN:

68022

Other (OTH)

AF:

0.000473

AC:

AN:

2114

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.523

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

Alfa

AF:

0.000394

Hom.:

Bravo

AF:

0.000196

EpiCase

AF:

0.000218

EpiControl

AF:

0.000178

ClinVar

Significance: Benign/Likely benign

Submissions summary: Benign:3

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:3

Dec 11, 2023

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Jun 05, 2018

Athena Diagnostics

Significance:Benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Sep 01, 2024

CeGaT Center for Human Genetics Tuebingen

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

SPTBN2: BP4, BP7 -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.85

CADD

Benign

0.43

(source)

DANN

Benign

0.64

PhyloP100

-3.4

Mutation Taster

=78/22

polymorphism

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.0

Details are displayed if max score is > 0.2

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

Publications

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over