rs6127

Variant names:

• chr1-169597075-C-A
• rs6127
• NM_003005.4:c.1807G>T

Your query was ambiguous. Multiple possible variants found:

• chr1-169597075-C-A
• chr1-169597075-C-G
• chr1-169597075-C-T

Variant summary

Our verdict is Uncertain significance. The variant received 1 ACMG points: 2P and 1B. PM2 BP4

The NM_003005.4(SELP):​c.1807G>T​(p.Asp603Tyr) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 15/20 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. D603N) has been classified as Benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: SELP NM_003005.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.410
• Publications: 0 publications found

Genes affected

SELP (HGNC:10721): (selectin P) This gene encodes a 140 kDa protein that is stored in the alpha-granules of platelets and Weibel-Palade bodies of endothelial cells. This protein redistributes to the plasma membrane during platelet activation and degranulation and mediates the interaction of activated endothelial cells or platelets with leukocytes. The membrane protein is a calcium-dependent receptor that binds to sialylated forms of Lewis blood group carbohydrate antigens on neutrophils and monocytes. Alternative splice variants may occur but are not well documented. [provided by RefSeq, Jul 2008]

ACMG classification

Our verdict: Uncertain_significance. The variant received 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.31397808).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SELP	NM_003005.4	c.1807G>T	p.Asp603Tyr	missense_variant	Exon 11 of 17	ENST00000263686.11	NP_002996.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SELP	ENST00000263686.11	c.1807G>T	p.Asp603Tyr	missense_variant	Exon 11 of 17	1	NM_003005.4	ENSP00000263686.5

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 47

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.087
BayesDel_addAF	Benign	-0.12	T
BayesDel_noAF	Benign	-0.41
CADD	Benign	13
DANN	Benign	0.95
DEOGEN2	Benign	0.048	T;.;T;T
Eigen	Benign	-0.63
Eigen_PC	Benign	-0.82
FATHMM_MKL	Benign	0.012	N
LIST_S2	Benign	0.27	T;T;T;T
M_CAP	Benign	0.055	D
MetaRNN	Benign	0.31	T;T;T;T
MetaSVM	Benign	-0.92	T
PhyloP100		-0.41
PrimateAI	Benign	0.29	T
PROVEAN	Uncertain	-3.1	D;D;D;D
REVEL	Benign	0.19
Sift	Benign	0.030	D;D;D;D
Sift4G	Uncertain	0.024	D;D;D;D
Vest4		0.30, 0.30, 0.34
MutPred		0.62		.;Loss of disorder (P = 0.0088);.;.;
MVP		0.75
MPC		0.096
ClinPred		0.55	D
GERP RS		-1.8
gMVP		0.43
Mutation Taster		=98/2	polymorphism

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: rs6127; hg19: chr1-169566313;