rs6667434

Variant names:

• chr1-154436624-A-G
• rs6667434
• NM_000565.4:c.949+514A>G

Your query was ambiguous. Multiple possible variants found:

• chr1-154436624-A-G
• chr1-154436624-A-T

Variant summary

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

The NM_000565.4(IL6R):​c.949+514A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.595 in 152,076 control chromosomes in the GnomAD database, including 27,368 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 0.60 (27368 hom., cov: 32)
• Consequence: IL6R NM_000565.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0640
• Publications: 24 publications found

Genes affected

IL6R (HGNC:6019): (interleukin 6 receptor) This gene encodes a subunit of the interleukin 6 (IL6) receptor complex. Interleukin 6 is a potent pleiotropic cytokine that regulates cell growth and differentiation and plays an important role in the immune response. The IL6 receptor is a protein complex consisting of this protein and interleukin 6 signal transducer (IL6ST/GP130/IL6-beta), a receptor subunit also shared by many other cytokines. Dysregulated production of IL6 and this receptor are implicated in the pathogenesis of many diseases, such as multiple myeloma, autoimmune diseases and prostate cancer. Alternatively spliced transcript variants encoding distinct isoforms have been identified in this gene. A pseudogene of this gene is found on chromosome 9. [provided by RefSeq, Aug 2020]

IL6R Gene-Disease associations (from GenCC):

• hyper-IgE recurrent infection syndrome 5, autosomal recessive

  Inheritance: AR Classification: STRONG, MODERATE, LIMITED Submitted by: Labcorp Genetics (formerly Invitae), ClinGen, Ambry Genetics

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 (AFR) allele frequency at 95% confidence interval = 0.659 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_000565.4. 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
	IL6R	NM_000565.4	MANE Select	c.949+514A>G		intron	N/A	NP_000556.1	P08887-1
	IL6R	NM_001382769.1		c.949+514A>G		intron	N/A	NP_001369698.1
	IL6R	NM_001382770.1		c.949+514A>G		intron	N/A	NP_001369699.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	IL6R	ENST00000368485.8	TSL:1 MANE Select	c.949+514A>G		intron	N/A	ENSP00000357470.3	P08887-1
	IL6R	ENST00000344086.8	TSL:1	c.949+514A>G		intron	N/A	ENSP00000340589.4	P08887-2
	IL6R	ENST00000622330.5	TSL:1	c.949+514A>G		intron	N/A	ENSP00000477739.1	A0A087WTB5

Frequencies

GnomAD3 genomes AF: 0.595 AC: 90411 AN: 151958 Hom.: 27322 Cov.: 32

Gnomad AFR AF: 0.665

Gnomad AMI AF: 0.723

Gnomad AMR AF: 0.659

Gnomad ASJ AF: 0.583

Gnomad EAS AF: 0.473

Gnomad SAS AF: 0.482

Gnomad FIN AF: 0.459

Gnomad MID AF: 0.566

Gnomad NFE AF: 0.576

Gnomad OTH AF: 0.583

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

GnomAD4 genome AF: 0.595 AC: 90512 AN: 152076 Hom.: 27368 Cov.: 32 AF XY: 0.586 AC XY: 43589 AN XY: 74344

African (AFR) AF: 0.666 AC: 27606 AN: 41480

American (AMR) AF: 0.659 AC: 10072 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.583 AC: 2020 AN: 3464

East Asian (EAS) AF: 0.474 AC: 2445 AN: 5162

South Asian (SAS) AF: 0.483 AC: 2331 AN: 4828

European-Finnish (FIN) AF: 0.459 AC: 4849 AN: 10572

Middle Eastern (MID) AF: 0.568 AC: 167 AN: 294

European-Non Finnish (NFE) AF: 0.576 AC: 39139 AN: 67972

Other (OTH) AF: 0.581 AC: 1224 AN: 2108

Alfa AF: 0.580 Hom.: 6271

Bravo AF: 0.618

Asia WGS AF: 0.489 AC: 1702 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	0.21
DANN	Benign	0.52
PhyloP100		-0.064
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: rs6667434; hg19: chr1-154409100;