Variant 6-159785684-T-C details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP4_ModerateBA1

The NM_030752.3(TCP1):c.378-188A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.205 in 791,580 control chromosomes in the GnomAD database, including 17,942 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 0.20 ( 3170 hom., cov: 33)

Exomes 𝑓: 0.21 ( 14772 hom. )

Consequence

TCP1
NM_030752.3 intron

Scores

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 1.80

Variant links:

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]

TCP1 links:

SNORA29 (HGNC:32619): (small nucleolar RNA, H/ACA box 29)

SNORA29 links:

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ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -10 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.25).

BA1

GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.388 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	Effect	#exon/exons	MANE
TCP1	NM_030752.3 linkuse as main transcript	c.378-188A>G	intron_variant		ENST00000321394.12
SNORA29	NR_002965.1 linkuse as main transcript	n.50A>G	non_coding_transcript_exon_variant	1/1
TCP1	NM_001008897.2 linkuse as main transcript	c.-88-188A>G	intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TCP1	ENST00000321394.12 linkuse as main transcript	c.378-188A>G		intron_variant		1	NM_030752.3	P1
SNORA29	ENST00000384183.1 linkuse as main transcript	n.50A>G		non_coding_transcript_exon_variant	1/1

Frequencies

GnomAD3 genomes

AF:

0.199

AC:

30206

AN:

151978

Hom.:

3169

Cov.:

show subpopulations

Gnomad AFR

AF:

0.181

Gnomad AMI

AF:

0.124

Gnomad AMR

AF:

0.205

Gnomad ASJ

AF:

0.118

Gnomad EAS

AF:

0.403

Gnomad SAS

AF:

0.280

Gnomad FIN

AF:

0.253

Gnomad MID

AF:

0.161

Gnomad NFE

AF:

0.183

Gnomad OTH

AF:

0.210

GnomAD3 exomes

AF:

0.210

AC:

49131

AN:

233618

Hom.:

5795

AF XY:

0.214

AC XY:

27382

AN XY:

128112

show subpopulations

Gnomad AFR exome

AF:

0.177

Gnomad AMR exome

AF:

0.174

Gnomad ASJ exome

AF:

0.121

Gnomad EAS exome

AF:

0.394

Gnomad SAS exome

AF:

0.268

Gnomad FIN exome

AF:

0.247

Gnomad NFE exome

AF:

0.185

Gnomad OTH exome

AF:

0.200

GnomAD4 exome

AF:

0.207

AC:

132349

AN:

639484

Hom.:

14772

Cov.:

AF XY:

0.210

AC XY:

73104

AN XY:

347824

show subpopulations

Gnomad4 AFR exome

AF:

0.176

Gnomad4 AMR exome

AF:

0.179

Gnomad4 ASJ exome

AF:

0.125

Gnomad4 EAS exome

AF:

0.380

Gnomad4 SAS exome

AF:

0.267

Gnomad4 FIN exome

AF:

0.241

Gnomad4 NFE exome

AF:

0.186

Gnomad4 OTH exome

AF:

0.198

GnomAD4 genome

AF:

0.199

AC:

30217

AN:

152096

Hom.:

3170

Cov.:

AF XY:

0.205

AC XY:

15235

AN XY:

74346

show subpopulations

Gnomad4 AFR

AF:

0.181

Gnomad4 AMR

AF:

0.204

Gnomad4 ASJ

AF:

0.118

Gnomad4 EAS

AF:

0.403

Gnomad4 SAS

AF:

0.281

Gnomad4 FIN

AF:

0.253

Gnomad4 NFE

AF:

0.183

Gnomad4 OTH

AF:

0.210

Alfa

AF:

0.178

Hom.:

843

Bravo

AF:

0.192

Asia WGS

AF:

0.300

AC:

1040

AN:

3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.25

CADD

Benign

DANN

Benign

0.91

RBP_binding_hub_radar

0.0

RBP_regulation_power_radar

1.1

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

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Computational scores

Splicing

Publications

LitVar

Other links and lift over