5-685633-G-A

Position:

• chr5-685633-G-A

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_007030.3(TPPP):​c.-4-7569C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.387 in 152,140 control chromosomes in the GnomAD database, including 11,526 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.39 (11526 hom., cov: 34)
• Consequence: TPPP NM_007030.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.88

Genes affected

TPPP (HGNC:24164): (tubulin polymerization promoting protein) Enables several functions, including GTPase activity; magnesium ion binding activity; and protein homodimerization activity. Involved in several processes, including microtubule cytoskeleton organization; negative regulation of tubulin deacetylation; and positive regulation of protein polymerization. Located in several cellular components, including mitochondrion; mitotic spindle; and perinuclear region of cytoplasm. Colocalizes with microtubule and microtubule bundle. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.544 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
TPPP	NM_007030.3	c.-4-7569C>T		intron_variant		ENST00000360578.7	NP_008961.1
TPPP	XM_024454346.1	c.-4-7569C>T		intron_variant			XP_024310114.1
TPPP	XM_047416674.1	c.-5+6928C>T		intron_variant			XP_047272630.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
TPPP	ENST00000360578.7	c.-4-7569C>T		intron_variant		1	NM_007030.3	ENSP00000353785	P1

Frequencies

GnomAD3 genomes AF: 0.387 AC: 58842 AN: 152022 Hom.: 11516 Cov.: 34

Gnomad AFR AF: 0.361

Gnomad AMI AF: 0.375

Gnomad AMR AF: 0.436

Gnomad ASJ AF: 0.391

Gnomad EAS AF: 0.561

Gnomad SAS AF: 0.392

Gnomad FIN AF: 0.370

Gnomad MID AF: 0.481

Gnomad NFE AF: 0.379

Gnomad OTH AF: 0.420

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

GnomAD4 genome AF: 0.387 AC: 58895 AN: 152140 Hom.: 11526 Cov.: 34 AF XY: 0.388 AC XY: 28886 AN XY: 74384

Gnomad4 AFR AF: 0.361

Gnomad4 AMR AF: 0.436

Gnomad4 ASJ AF: 0.391

Gnomad4 EAS AF: 0.561

Gnomad4 SAS AF: 0.392

Gnomad4 FIN AF: 0.370

Gnomad4 NFE AF: 0.379

Gnomad4 OTH AF: 0.420

Alfa AF: 0.385 Hom.: 14342

Bravo AF: 0.396

Asia WGS AF: 0.466 AC: 1619 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.56
DANN	Benign	0.36

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: rs386057; hg19: chr5-685748;