chr12-6444664-T-TG

Position:

• chr12-6444664-T-TG

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP6_Moderate BA1

The NM_001413266.1(CD27):​c.-315+554dupG variant causes a intron change involving the alteration of a non-conserved nucleotide. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.28 (1866 hom., cov: 0)
• Consequence: CD27 NM_001413266.1 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -2.06

Genes affected

CD27-AS1 (HGNC:):

CD27 (HGNC:11922): (CD27 molecule) The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is required for generation and long-term maintenance of T cell immunity. It binds to ligand CD70, and plays a key role in regulating B-cell activation and immunoglobulin synthesis. This receptor transduces signals that lead to the activation of NF-kappaB and MAPK8/JNK. Adaptor proteins TRAF2 and TRAF5 have been shown to mediate the signaling process of this receptor. CD27-binding protein (SIVA), a proapoptotic protein, can bind to this receptor and is thought to play an important role in the apoptosis induced by this receptor. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -10 ACMG points.

• BP6: Variant 12-6444664-T-TG is Benign according to our data. Variant chr12-6444664-T-TG is described in ClinVar as [Benign]. Clinvar id is 1260079.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.399 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
CD27	NM_001413266.1	c.-315+554dupG		intron_variant			NP_001400195.1
CD27	NM_001413267.1	c.-403+554dupG		intron_variant			NP_001400196.1
CD27	NM_001413268.1	c.-315+66dupG		intron_variant			NP_001400197.1
CD27-AS1	NR_015382.2	n.1517-948dupC		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
CD27-AS1	ENST00000399492.6	n.485-948dupC		intron_variant		1
CD27-AS1	ENST00000417058.6	n.814-948dupC		intron_variant		1
CD27-AS1	ENST00000537003.2	n.1980-948dupC		intron_variant		1

Frequencies

GnomAD3 genomes AF: 0.275 AC: 19469 AN: 70710 Hom.: 1861 Cov.: 0

Gnomad AFR AF: 0.177

Gnomad AMI AF: 0.471

Gnomad AMR AF: 0.338

Gnomad ASJ AF: 0.376

Gnomad EAS AF: 0.423

Gnomad SAS AF: 0.195

Gnomad FIN AF: 0.307

Gnomad MID AF: 0.307

Gnomad NFE AF: 0.289

Gnomad OTH AF: 0.300

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

GnomAD4 genome AF: 0.275 AC: 19474 AN: 70720 Hom.: 1866 Cov.: 0 AF XY: 0.272 AC XY: 8793 AN XY: 32270

Gnomad4 AFR AF: 0.177

Gnomad4 AMR AF: 0.340

Gnomad4 ASJ AF: 0.376

Gnomad4 EAS AF: 0.423

Gnomad4 SAS AF: 0.194

Gnomad4 FIN AF: 0.307

Gnomad4 NFE AF: 0.289

Gnomad4 OTH AF: 0.302

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Jun 19, 2021

- -

Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs57782770; hg19: chr12-6553830;