NM_030752.3:c.*390A>G

Variant names:

• chr6-159778655-T-C
• rs15982
• NM_030752.3:c.*390A>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_030752.3(TCP1):​c.*390A>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 0.752 in 1,612,640 control chromosomes in the GnomAD database, including 458,906 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 0.70 (38340 hom., cov: 31)
  • Exomes 𝑓: 0.76 (420566 hom.)
• Consequence: TCP1 NM_030752.3 3_prime_UTR
• Scores: Splicing: ADA: 0.00006833
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.209
• Publications: 29 publications found

Genes affected

TCP1 (HGNC:11655): (t-complex 1) The protein encoded by this gene is a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Alternate transcriptional splice variants of this gene, encoding different isoforms, have been characterized. In addition, three pseudogenes that appear to be derived from this gene have been found. [provided by RefSeq, Jun 2010]

ACAT2 (HGNC:94): (acetyl-CoA acetyltransferase 2) The product of this gene is an enzyme involved in lipid metabolism, and it encodes cytosolic acetoacetyl-CoA thiolase. This gene shows complementary overlapping with the 3-prime region of the TCP1 gene in both mouse and human. These genes are encoded on opposite strands of DNA, as well as in opposite transcriptional orientation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2014]

ACAT2 Gene-Disease associations (from GenCC):

• acetyl-CoA acetyltransferase-2 deficiency

  Inheritance: AR, Unknown Classification: LIMITED, NO_KNOWN Submitted by: Ambry Genetics, ClinGen

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.74).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.757 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_030752.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TCP1	NM_030752.3	MANE Select	c.*390A>G		3_prime_UTR	Exon 12 of 12	NP_110379.2	P17987
	ACAT2	NM_005891.3	MANE Select	c.1024-4T>C		splice_region intron	N/A	NP_005882.2	Q9BWD1-1
	TCP1	NM_001008897.2		c.*390A>G		3_prime_UTR	Exon 11 of 11	NP_001008897.1	E7EQR6

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TCP1	ENST00000321394.12	TSL:1 MANE Select	c.*390A>G		3_prime_UTR	Exon 12 of 12	ENSP00000317334.7	P17987
	ACAT2	ENST00000367048.5	TSL:1 MANE Select	c.1024-4T>C		splice_region intron	N/A	ENSP00000356015.4	Q9BWD1-1
	TCP1	ENST00000934596.1		c.*390A>G		3_prime_UTR	Exon 12 of 12	ENSP00000604655.1

Frequencies

GnomAD3 genomes AF: 0.702 AC: 106631 AN: 151898 Hom.: 38334 Cov.: 31

Gnomad AFR AF: 0.559

Gnomad AMI AF: 0.621

Gnomad AMR AF: 0.766

Gnomad ASJ AF: 0.681

Gnomad EAS AF: 0.586

Gnomad SAS AF: 0.780

Gnomad FIN AF: 0.824

Gnomad MID AF: 0.665

Gnomad NFE AF: 0.761

Gnomad OTH AF: 0.709

GnomAD2 exomes AF: 0.746 AC: 186772 AN: 250410 AF XY: 0.748

Gnomad AFR exome AF: 0.548

Gnomad AMR exome AF: 0.823

Gnomad ASJ exome AF: 0.678

Gnomad EAS exome AF: 0.578

Gnomad FIN exome AF: 0.822

Gnomad NFE exome AF: 0.763

Gnomad OTH exome AF: 0.751

GnomAD4 exome AF: 0.757 AC: 1105470 AN: 1460624 Hom.: 420566 Cov.: 41 AF XY: 0.757 AC XY: 549931 AN XY: 726636

African (AFR) AF: 0.553 AC: 18484 AN: 33448

American (AMR) AF: 0.820 AC: 36637 AN: 44690

Ashkenazi Jewish (ASJ) AF: 0.677 AC: 17677 AN: 26106

East Asian (EAS) AF: 0.564 AC: 22361 AN: 39674

South Asian (SAS) AF: 0.769 AC: 66310 AN: 86180

European-Finnish (FIN) AF: 0.823 AC: 43950 AN: 53408

Middle Eastern (MID) AF: 0.701 AC: 4044 AN: 5768

European-Non Finnish (NFE) AF: 0.767 AC: 852162 AN: 1111004

Other (OTH) AF: 0.727 AC: 43845 AN: 60346

GnomAD4 genome AF: 0.702 AC: 106672 AN: 152016 Hom.: 38340 Cov.: 31 AF XY: 0.706 AC XY: 52456 AN XY: 74276

African (AFR) AF: 0.559 AC: 23164 AN: 41426

American (AMR) AF: 0.766 AC: 11707 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.681 AC: 2359 AN: 3466

East Asian (EAS) AF: 0.585 AC: 3016 AN: 5154

South Asian (SAS) AF: 0.778 AC: 3754 AN: 4824

European-Finnish (FIN) AF: 0.824 AC: 8707 AN: 10566

Middle Eastern (MID) AF: 0.653 AC: 192 AN: 294

European-Non Finnish (NFE) AF: 0.761 AC: 51729 AN: 67992

Other (OTH) AF: 0.703 AC: 1481 AN: 2108

Alfa AF: 0.739 Hom.: 77664

Bravo AF: 0.688

Asia WGS AF: 0.662 AC: 2299 AN: 3478

EpiCase AF: 0.750

EpiControl AF: 0.759

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.74
CADD	Benign	7.0
DANN	Benign	0.79
PhyloP100		0.21
Mutation Taster		=99/1	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
dbscSNV1_ADA	Benign	0.000068
dbscSNV1_RF	Benign	0.0020
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

Other links and lift over

dbSNP: rs15982; hg19: chr6-160199687; COSMIC: COSV58458980; COSMIC: COSV58458980;