chr12-71925061-A-G

Variant names:

• chr12-71925061-A-G
• rs17110432
• ENST00000550746.5:c.*1857A>G

Variant summary

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

The ENST00000550746.5(TBC1D15):​c.*1857A>G variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0964 in 151,688 control chromosomes in the GnomAD database, including 845 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 0.096 (845 hom., cov: 31)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: TBC1D15 ENST00000550746.5 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.31

Genes affected

TBC1D15 (HGNC:25694): (TBC1 domain family member 15) This gene encodes a member of the Ras-like proteins in brain-GTPase activating protein superfamily that share a conserved Tre-2/Bub2/Cdc16 domain. The encoded protein interacts with Ras-like protein in brain 5A and may function as a regulator of intracellular trafficking. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.78).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.154 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TBC1D15	ENST00000550746.5	c.*1857A>G		3_prime_UTR_variant	Exon 18 of 18	1		ENSP00000448182.1

Frequencies

GnomAD3 genomes AF: 0.0961 AC: 14572 AN: 151574 Hom.: 839 Cov.: 31

Gnomad AFR AF: 0.153

Gnomad AMI AF: 0.0407

Gnomad AMR AF: 0.0830

Gnomad ASJ AF: 0.0334

Gnomad EAS AF: 0.162

Gnomad SAS AF: 0.109

Gnomad FIN AF: 0.0698

Gnomad MID AF: 0.0728

Gnomad NFE AF: 0.0672

Gnomad OTH AF: 0.0849

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 6 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 6

Gnomad4 NFE exome AF: 0.00

GnomAD4 genome AF: 0.0964 AC: 14619 AN: 151688 Hom.: 845 Cov.: 31 AF XY: 0.0970 AC XY: 7193 AN XY: 74122

Gnomad4 AFR AF: 0.153

Gnomad4 AMR AF: 0.0839

Gnomad4 ASJ AF: 0.0334

Gnomad4 EAS AF: 0.163

Gnomad4 SAS AF: 0.109

Gnomad4 FIN AF: 0.0698

Gnomad4 NFE AF: 0.0672

Gnomad4 OTH AF: 0.0882

Alfa AF: 0.0821 Hom.: 76

Bravo AF: 0.101

Asia WGS AF: 0.162 AC: 560 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	9.5
DANN	Benign	0.76

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs17110432; hg19: chr12-72318841;