NM_007360.4:c.214A>G

Variant names:

• chr12-10379727-T-C
• rs2255336
• NM_007360.4:c.214A>G

Variant summary

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

The NM_007360.4(KLRK1):​c.214A>G​(p.Thr72Ala) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.802 in 1,610,626 control chromosomes in the GnomAD database, including 520,524 homozygotes. In-silico tool predicts a benign outcome for this variant. 14/19 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.75 (43298 hom., cov: 31)
  • Exomes 𝑓: 0.81 (477226 hom.)
• Consequence: KLRK1 NM_007360.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.60
• Publications: 73 publications found

Genes affected

KLRK1 (HGNC:18788): (killer cell lectin like receptor K1) Natural killer (NK) cells are lymphocytes that can mediate lysis of certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. NK cells preferentially express several calcium-dependent (C-type) lectins, which have been implicated in the regulation of NK cell function. The NKG2 gene family is located within the NK complex, a region that contains several C-type lectin genes preferentially expressed in NK cells. This gene encodes a member of the NKG2 family. The encoded transmembrane protein is characterized by a type II membrane orientation (has an extracellular C terminus) and the presence of a C-type lectin domain. It binds to a diverse family of ligands that include MHC class I chain-related A and B proteins and UL-16 binding proteins, where ligand-receptor interactions can result in the activation of NK and T cells. The surface expression of these ligands is important for the recognition of stressed cells by the immune system, and thus this protein and its ligands are therapeutic targets for the treatment of immune diseases and cancers. Read-through transcription exists between this gene and the upstream KLRC4 (killer cell lectin-like receptor subfamily C, member 4) family member in the same cluster. [provided by RefSeq, Dec 2010]

KLRC4-KLRK1 (HGNC:48357): (KLRC4-KLRK1 readthrough) This locus represents naturally occurring read-through transcription between the neighboring KLRC4 (killer cell lectin-like receptor subfamily C, member 4) and KLRK1 (killer cell lectin-like receptor subfamily K, member 1) genes on chromosome 12. The read-through transcript includes an alternate 5' exon and lacks a significant portion of the KLRC4 coding sequence, including the start codon, and it thus encodes the KLRK1 protein. [provided by RefSeq, Dec 2010]

KLRK1-AS1 (HGNC:54868): (KLRK1 antisense RNA 1)

ACMG classification

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

• BP4: Computational evidence support a benign effect (MetaRNN=1.0851428E-6).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.862 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_007360.4. 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
	KLRK1	NM_007360.4	MANE Select	c.214A>G	p.Thr72Ala	missense	Exon 4 of 8	NP_031386.2	P26718-1
	KLRC4-KLRK1	NM_001199805.1		c.214A>G	p.Thr72Ala	missense	Exon 9 of 13	NP_001186734.1	P26718-1
	KLRK1-AS1	NR_120430.1		n.393T>C		non_coding_transcript_exon	Exon 3 of 4

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	KLRK1	ENST00000240618.11	TSL:1 MANE Select	c.214A>G	p.Thr72Ala	missense	Exon 4 of 8	ENSP00000240618.6	P26718-1
	KLRK1	ENST00000540818.5	TSL:1	c.214A>G	p.Thr72Ala	missense	Exon 3 of 7	ENSP00000446003.1	P26718-1
	KLRC4-KLRK1	ENST00000539300.5	TSL:2	n.*411A>G		non_coding_transcript_exon	Exon 9 of 13	ENSP00000455951.1	H3BQV0

Frequencies

GnomAD3 genomes AF: 0.747 AC: 113519 AN: 151912 Hom.: 43277 Cov.: 31

Gnomad AFR AF: 0.577

Gnomad AMI AF: 0.747

Gnomad AMR AF: 0.828

Gnomad ASJ AF: 0.796

Gnomad EAS AF: 0.773

Gnomad SAS AF: 0.884

Gnomad FIN AF: 0.810

Gnomad MID AF: 0.769

Gnomad NFE AF: 0.808

Gnomad OTH AF: 0.760

GnomAD2 exomes AF: 0.808 AC: 201579 AN: 249454 AF XY: 0.812

Gnomad AFR exome AF: 0.576

Gnomad AMR exome AF: 0.888

Gnomad ASJ exome AF: 0.788

Gnomad EAS exome AF: 0.759

Gnomad FIN exome AF: 0.810

Gnomad NFE exome AF: 0.806

Gnomad OTH exome AF: 0.801

GnomAD4 exome AF: 0.807 AC: 1177745 AN: 1458596 Hom.: 477226 Cov.: 45 AF XY: 0.810 AC XY: 587957 AN XY: 725450

African (AFR) AF: 0.570 AC: 19031 AN: 33392

American (AMR) AF: 0.882 AC: 39219 AN: 44472

Ashkenazi Jewish (ASJ) AF: 0.789 AC: 20560 AN: 26046

East Asian (EAS) AF: 0.789 AC: 31186 AN: 39538

South Asian (SAS) AF: 0.880 AC: 75175 AN: 85430

European-Finnish (FIN) AF: 0.809 AC: 43120 AN: 53306

Middle Eastern (MID) AF: 0.788 AC: 4520 AN: 5734

European-Non Finnish (NFE) AF: 0.808 AC: 897503 AN: 1110418

Other (OTH) AF: 0.787 AC: 47431 AN: 60260

GnomAD4 genome AF: 0.747 AC: 113585 AN: 152030 Hom.: 43298 Cov.: 31 AF XY: 0.749 AC XY: 55700 AN XY: 74324

African (AFR) AF: 0.577 AC: 23910 AN: 41428

American (AMR) AF: 0.828 AC: 12645 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.796 AC: 2760 AN: 3468

East Asian (EAS) AF: 0.774 AC: 4007 AN: 5180

South Asian (SAS) AF: 0.884 AC: 4258 AN: 4818

European-Finnish (FIN) AF: 0.810 AC: 8554 AN: 10564

Middle Eastern (MID) AF: 0.776 AC: 228 AN: 294

European-Non Finnish (NFE) AF: 0.808 AC: 54933 AN: 67982

Other (OTH) AF: 0.763 AC: 1609 AN: 2110

Alfa AF: 0.786 Hom.: 182736

Bravo AF: 0.738

TwinsUK AF: 0.807 AC: 2994

ALSPAC AF: 0.799 AC: 3080

ESP6500AA AF: 0.579 AC: 2552

ESP6500EA AF: 0.800 AC: 6877

ExAC AF: 0.803 AC: 97496

Asia WGS AF: 0.816 AC: 2836 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.070
BayesDel_addAF	Benign	-0.87	T
BayesDel_noAF	Benign	-0.87
CADD	Benign	1.3
DANN	Benign	0.91
Eigen	Benign	-1.2
Eigen_PC	Benign	-1.3
FATHMM_MKL	Benign	0.0069	N
LIST_S2	Benign	0.30	T
MetaRNN	Benign	0.0000011	T
MetaSVM	Benign	-1.1	T
PhyloP100		-1.6
PrimateAI	Benign	0.23	T
PROVEAN	Benign	-0.60	N
REVEL	Benign	0.010
Sift	Benign	0.96	T
Sift4G	Benign	0.27	T
Vest4		0.044
MPC		0.18
ClinPred		0.00087	T
GERP RS		-1.4
gMVP		0.14
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: rs2255336; hg19: chr12-10532326; COSMIC: COSV53698409; COSMIC: COSV53698409;