chr6-14122849-A-G

Variant names:

• chr6-14122849-A-G
• rs12205252
• NM_004233.4:c.153+4784A>G

Variant summary

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

The NM_004233.4(CD83):​c.153+4784A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.161 in 152,286 control chromosomes in the GnomAD database, including 2,446 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 (2446 hom., cov: 32)
• Consequence: CD83 NM_004233.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0130
• Publications: 5 publications found

Genes affected

CD83 (HGNC:1703): (CD83 molecule) The protein encoded by this gene is a single-pass type I membrane protein and member of the immunoglobulin superfamily of receptors. The encoded protein may be involved in the regulation of antigen presentation. A soluble form of this protein can bind to dendritic cells and inhibit their maturation. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.83).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.219 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CD83	NM_004233.4	c.153+4784A>G		intron_variant	Intron 2 of 4	ENST00000379153.4	NP_004224.1
CD83	NM_001040280.3	c.153+4784A>G		intron_variant	Intron 2 of 4		NP_001035370.1
CD83	NM_001251901.1	c.-25+4784A>G		intron_variant	Intron 2 of 4		NP_001238830.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CD83	ENST00000379153.4	c.153+4784A>G		intron_variant	Intron 2 of 4	1	NM_004233.4	ENSP00000368450.3
CD83	ENST00000612003.5	c.-25+4784A>G		intron_variant	Intron 2 of 4	4		ENSP00000480760.1

Frequencies

GnomAD3 genomes AF: 0.161 AC: 24501 AN: 152168 Hom.: 2448 Cov.: 32

Gnomad AFR AF: 0.0601

Gnomad AMI AF: 0.394

Gnomad AMR AF: 0.164

Gnomad ASJ AF: 0.191

Gnomad EAS AF: 0.00231

Gnomad SAS AF: 0.123

Gnomad FIN AF: 0.220

Gnomad MID AF: 0.253

Gnomad NFE AF: 0.222

Gnomad OTH AF: 0.176

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

GnomAD4 genome AF: 0.161 AC: 24504 AN: 152286 Hom.: 2446 Cov.: 32 AF XY: 0.160 AC XY: 11879 AN XY: 74460

African (AFR) AF: 0.0602 AC: 2501 AN: 41576

American (AMR) AF: 0.164 AC: 2503 AN: 15308

Ashkenazi Jewish (ASJ) AF: 0.191 AC: 664 AN: 3470

East Asian (EAS) AF: 0.00231 AC: 12 AN: 5186

South Asian (SAS) AF: 0.124 AC: 598 AN: 4824

European-Finnish (FIN) AF: 0.220 AC: 2330 AN: 10598

Middle Eastern (MID) AF: 0.245 AC: 72 AN: 294

European-Non Finnish (NFE) AF: 0.222 AC: 15096 AN: 68008

Other (OTH) AF: 0.175 AC: 370 AN: 2114

Alfa AF: 0.179 Hom.: 425

Bravo AF: 0.153

Asia WGS AF: 0.0610 AC: 211 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
CADD	Benign	2.1
DANN	Benign	0.50
PhyloP100		-0.013
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: rs12205252; hg19: chr6-14123080;