chr1-235379947-CA-C

Variant names:

• chr1-235379947-CA-C
• rs36068852
• NM_003193.5:c.-31-55delA

Variant summary

Our verdict is Benign. Variant got -8 ACMG points: 0P and 8B. BA1

The NM_003193.5(TBCE):​c.-31-55delA variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0545 in 710,486 control chromosomes in the GnomAD database, with no homozygous occurrence. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.00094 (0 hom., cov: 0)
  • Exomes 𝑓: 0.067 (0 hom.)
• Consequence: TBCE NM_003193.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.566

Genes affected

TBCE (HGNC:11582): (tubulin folding cofactor E) Cofactor E is one of four proteins (cofactors A, D, E, and C) involved in the pathway leading to correctly folded beta-tubulin from folding intermediates. Cofactors A and D are believed to play a role in capturing and stabilizing beta-tubulin intermediates in a quasi-native confirmation. Cofactor E binds to the cofactor D/beta-tubulin complex; interaction with cofactor C then causes the release of beta-tubulin polypeptides that are committed to the native state. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

ENSG00000285053 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -8 ACMG points.

• BA1: GnomAdExome4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.0835 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TBCE	NM_003193.5	c.-31-55delA		intron_variant	Intron 1 of 16	ENST00000642610.2	NP_003184.1
TBCE	NM_001287801.2	c.-31-55delA		intron_variant	Intron 1 of 17		NP_001274730.1
TBCE	NM_001079515.3	c.-31-55delA		intron_variant	Intron 1 of 16		NP_001072983.1
TBCE	NM_001287802.2	c.-341-55delA		intron_variant	Intron 1 of 15		NP_001274731.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TBCE	ENST00000642610.2	c.-31-71delA		intron_variant	Intron 1 of 16		NM_003193.5	ENSP00000494796.1
ENSG00000285053	ENST00000645655.1	c.-31-71delA		intron_variant	Intron 4 of 19			ENSP00000495202.1

Frequencies

GnomAD3 genomes AF: 0.000942 AC: 125 AN: 132706 Hom.: 0 Cov.: 0

Gnomad AFR AF: 0.000334

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.000863

Gnomad ASJ AF: 0.00122

Gnomad EAS AF: 0.000661

Gnomad SAS AF: 0.000251

Gnomad FIN AF: 0.00591

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.000804

Gnomad OTH AF: 0.00111

GnomAD4 exome AF: 0.0668 AC: 38586 AN: 577750 Hom.: 0 AF XY: 0.0680 AC XY: 20623 AN XY: 303258

Gnomad4 AFR exome AF: 0.0294

Gnomad4 AMR exome AF: 0.0769

Gnomad4 ASJ exome AF: 0.0631

Gnomad4 EAS exome AF: 0.0666

Gnomad4 SAS exome AF: 0.0855

Gnomad4 FIN exome AF: 0.0715

Gnomad4 NFE exome AF: 0.0648

Gnomad4 OTH exome AF: 0.0632

GnomAD4 genome AF: 0.000942 AC: 125 AN: 132736 Hom.: 0 Cov.: 0 AF XY: 0.00117 AC XY: 74 AN XY: 63076

Gnomad4 AFR AF: 0.000333

Gnomad4 AMR AF: 0.000862

Gnomad4 ASJ AF: 0.00122

Gnomad4 EAS AF: 0.000663

Gnomad4 SAS AF: 0.000251

Gnomad4 FIN AF: 0.00591

Gnomad4 NFE AF: 0.000805

Gnomad4 OTH AF: 0.00111

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

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

LitVar

Other links and lift over

dbSNP: rs36068852; hg19: chr1-235543262;