rs11230559

Variant names:

• chr11-61002062-T-C
• rs11230559
• NM_006725.5:c.50-4512T>C

Variant summary

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

The NM_006725.5(CD6):​c.50-4512T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.164 in 152,218 control chromosomes in the GnomAD database, including 2,848 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 0.16 (2848 hom., cov: 32)
• Consequence: CD6 NM_006725.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.104
• Publications: 9 publications found

Genes affected

CD6 (HGNC:1691): (CD6 molecule) This gene encodes a protein found on the outer membrane of T-lymphocytes as well as some other immune cells. The encoded protein contains three scavenger receptor cysteine-rich (SRCR) domains and a binding site for an activated leukocyte cell adhesion molecule. The gene product is important for continuation of T cell activation. This gene may be associated with susceptibility to multiple sclerosis (PMID: 19525953, 21849685). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.234 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_006725.5. 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
	CD6	NM_006725.5	MANE Select	c.50-4512T>C		intron	N/A	NP_006716.3
	CD6	NM_001254750.2		c.50-4512T>C		intron	N/A	NP_001241679.1
	CD6	NM_001254751.2		c.50-4512T>C		intron	N/A	NP_001241680.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CD6	ENST00000313421.11	TSL:1 MANE Select	c.50-4512T>C		intron	N/A	ENSP00000323280.7
	CD6	ENST00000352009.9	TSL:1	c.50-4512T>C		intron	N/A	ENSP00000340628.5
	CD6	ENST00000452451.6	TSL:1	c.50-4512T>C		intron	N/A	ENSP00000390676.2

Frequencies

GnomAD3 genomes AF: 0.165 AC: 25034 AN: 152100 Hom.: 2848 Cov.: 32

Gnomad AFR AF: 0.0475

Gnomad AMI AF: 0.258

Gnomad AMR AF: 0.157

Gnomad ASJ AF: 0.445

Gnomad EAS AF: 0.0225

Gnomad SAS AF: 0.0701

Gnomad FIN AF: 0.167

Gnomad MID AF: 0.320

Gnomad NFE AF: 0.237

Gnomad OTH AF: 0.207

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

GnomAD4 genome AF: 0.164 AC: 25022 AN: 152218 Hom.: 2848 Cov.: 32 AF XY: 0.160 AC XY: 11908 AN XY: 74410

African (AFR) AF: 0.0475 AC: 1974 AN: 41556

American (AMR) AF: 0.157 AC: 2397 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.445 AC: 1542 AN: 3468

East Asian (EAS) AF: 0.0224 AC: 116 AN: 5186

South Asian (SAS) AF: 0.0706 AC: 341 AN: 4830

European-Finnish (FIN) AF: 0.167 AC: 1764 AN: 10582

Middle Eastern (MID) AF: 0.310 AC: 91 AN: 294

European-Non Finnish (NFE) AF: 0.237 AC: 16132 AN: 68002

Other (OTH) AF: 0.204 AC: 430 AN: 2112

Alfa AF: 0.197 Hom.: 622

Bravo AF: 0.163

Asia WGS AF: 0.0570 AC: 199 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	3.4
DANN	Benign	0.68
PhyloP100		0.10
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs11230559; hg19: chr11-60769534;