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Y-1202479-C-T

Position:

• chrY-1202479-C-T

Variant summary

Our verdict is Likely benign. Variant got -2 ACMG points: 0P and 2B. BP4_Moderate

The ENST00000711254.1(CRLF2):​c.406G>A​(p.Val136Met) variant causes a missense change involving the alteration of a non-conserved nucleotide. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as not provided (no stars).

• Frequency: Genomes: not found (cov:)
• Consequence: CRLF2 ENST00000711254.1 missense
• Clinical Significance: not provided no classification provided O:1
• Conservation: PhyloP100: -0.0500

Genes affected

CRLF2 (HGNC:14281): (cytokine receptor like factor 2) This gene encodes a member of the type I cytokine receptor family. The encoded protein is a receptor for thymic stromal lymphopoietin (TSLP). Together with the interleukin 7 receptor (IL7R), the encoded protein and TSLP activate STAT3, STAT5, and JAK2 pathways, which control processes such as cell proliferation and development of the hematopoietic system. Rearrangement of this gene with immunoglobulin heavy chain gene (IGH) on chromosome 14, or with P2Y purinoceptor 8 gene (P2RY8) on the same X or Y chromosomes is associated with B-progenitor acute lymphoblastic leukemia (ALL) and Down syndrome ALL. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]

CRLF2_1 (HGNC:):

ACMG classification

Verdict is Likely_benign. Variant got -2 ACMG points.

• BP4: Computational evidence support a benign effect (Cadd=16.14).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
CRLF2_1	NM_022148.4_1	c.406G>A	p.Val136Met	missense_variant	4/8
CRLF2_1	NM_001012288.3_1	c.70G>A	p.Val24Met	missense_variant	3/7
CRLF2_1	XM_011545634.3	c.403G>A	p.Val135Met	missense_variant	4/8		XP_011543936.1
CRLF2_1	NR_110830.2_1	n.418G>A		non_coding_transcript_exon_variant	4/8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
CRLF2	ENST00000711254.1	c.406G>A	p.Val136Met	missense_variant	4/8	1		ENSP00000518625.1
CRLF2	ENST00000711256.1	c.70G>A	p.Val24Met	missense_variant	3/7	1		ENSP00000518623.1
CRLF2	ENST00000711255.1	n.403G>A		non_coding_transcript_exon_variant	4/8	5		ENSP00000518624.1

Frequencies

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

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

Alfa AF: 0.0248 Hom.: 81

ClinVar

Significance: not provided

Submissions summary: Other:1

Revision: no classification provided

Submissions by phenotype

not specified Other:1

not provided, no classification provided

reference population

ITMI

Sep 19, 2013

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.57
CADD	Benign	16

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs138899368; hg19: chrY-1271349;