chrY-2787036-T-G

Position:

• chrY-2787036-T-G

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM1 BP4 BP6

The NM_003140.3(SRY):​c.568A>C​(p.Ser190Arg) 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 Benign (no stars).

• Frequency: Genomes: not found (cov: 0)
• Consequence: SRY NM_003140.3 missense
• Clinical Significance: Benign no assertion criteria provided B:1
• Conservation: PhyloP100: 1.44

Genes affected

SRY (HGNC:11311): (sex determining region Y) This intronless gene encodes a transcription factor that is a member of the high mobility group (HMG)-box family of DNA-binding proteins. This protein is the testis-determining factor (TDF), which initiates male sex determination. Mutations in this gene give rise to XY females with gonadal dysgenesis (Swyer syndrome); translocation of part of the Y chromosome containing this gene to the X chromosome causes XX male syndrome. [provided by RefSeq, Jul 2008]

XGY2 (HGNC:34022): (XG Y-linked 2 (pseudogene))

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM1: In a chain Sex-determining region Y protein (size 203) in uniprot entity SRY_HUMAN there are 34 pathogenic changes around while only 1 benign (97%) in NM_003140.3
• BP4: Computational evidence support a benign effect (MetaRNN=0.33879828).
• BP6: Variant Y-2787036-T-G is Benign according to our data. Variant chrY-2787036-T-G is described in ClinVar as [Benign]. Clinvar id is 3242236.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SRY	NM_003140.3	c.568A>C	p.Ser190Arg	missense_variant	1/1	ENST00000383070.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SRY	ENST00000383070.2	c.568A>C	p.Ser190Arg	missense_variant	1/1		NM_003140.3	P1
XGY2	ENST00000681940.1	n.106+12297T>G		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes Cov.: 0

GnomAD4 exome Cov.: 0

GnomAD4 genome Cov.: 0

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: no assertion criteria provided

Submissions by phenotype

46,XY disorder of sex development Benign:1

Benign, no assertion criteria provided

clinical testing

Institute of Biochemistry, Molecular Biology and Biotechnology, University of Colombo

Jun 13, 2024

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.24
BayesDel_addAF	Uncertain	0.075	D
BayesDel_noAF	Benign	-0.13
CADD	Benign	17
DANN	Uncertain	0.99
DEOGEN2	Benign	0.17	T
FATHMM_MKL	Benign	0.54	D
LIST_S2	Benign	0.70	T
M_CAP	Pathogenic	1.0	D
MetaRNN	Benign	0.34	T
MetaSVM	Uncertain	0.22	D
MutationAssessor	Benign	1.6	L
MutationTaster	Benign	1.0	N
PROVEAN	Benign	-2.2	N
Sift	Benign	0.072	T
Sift4G	Benign	0.14	T
Polyphen		0.0010	B
Vest4		0.24
MutPred		0.32		Gain of catalytic residue at S190 (P = 0.0075);
MVP		0.98
MPC		0.67
ClinPred		0.22	T
GERP RS		0.64
Varity_R		0.31
gMVP		0.52

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		Details are displayed if max score is > 0.2

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

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chrY-2655077;