rs10497095

Variant names:

• chr2-152121474-G-A
• rs10497095
• NM_005843.6:c.1350-672C>T

Variant summary

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

The NM_005843.6(STAM2):​c.1350-672C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.212 in 152,000 control chromosomes in the GnomAD database, including 3,617 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 0.21 (3617 hom., cov: 31)
• Consequence: STAM2 NM_005843.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.23
• Publications: 2 publications found

Genes affected

STAM2 (HGNC:11358): (signal transducing adaptor molecule 2) The protein encoded by this gene is closely related to STAM, an adaptor protein involved in the downstream signaling of cytokine receptors, both of which contain a SH3 domain and the immunoreceptor tyrosine-based activation motif (ITAM). Similar to STAM, this protein acts downstream of JAK kinases, and is phosphorylated in response to cytokine stimulation. This protein and STAM thus are thought to exhibit compensatory effects on the signaling pathway downstream of JAK kinases upon cytokine stimulation. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.294 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_005843.6. 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
	STAM2	NM_005843.6	MANE Select	c.1350-672C>T		intron	N/A	NP_005834.4

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	STAM2	ENST00000263904.5	TSL:1 MANE Select	c.1350-672C>T		intron	N/A	ENSP00000263904.4	O75886-1
	STAM2	ENST00000865052.1		c.1404-672C>T		intron	N/A	ENSP00000535111.1
	STAM2	ENST00000968933.1		c.1305-672C>T		intron	N/A	ENSP00000638992.1

Frequencies

GnomAD3 genomes AF: 0.211 AC: 32094 AN: 151884 Hom.: 3600 Cov.: 31

Gnomad AFR AF: 0.153

Gnomad AMI AF: 0.307

Gnomad AMR AF: 0.300

Gnomad ASJ AF: 0.231

Gnomad EAS AF: 0.258

Gnomad SAS AF: 0.220

Gnomad FIN AF: 0.300

Gnomad MID AF: 0.152

Gnomad NFE AF: 0.208

Gnomad OTH AF: 0.193

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

GnomAD4 genome AF: 0.212 AC: 32154 AN: 152000 Hom.: 3617 Cov.: 31 AF XY: 0.216 AC XY: 16079 AN XY: 74278

African (AFR) AF: 0.153 AC: 6341 AN: 41488

American (AMR) AF: 0.301 AC: 4595 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.231 AC: 801 AN: 3464

East Asian (EAS) AF: 0.257 AC: 1325 AN: 5156

South Asian (SAS) AF: 0.221 AC: 1063 AN: 4810

European-Finnish (FIN) AF: 0.300 AC: 3155 AN: 10528

Middle Eastern (MID) AF: 0.158 AC: 46 AN: 292

European-Non Finnish (NFE) AF: 0.208 AC: 14120 AN: 67968

Other (OTH) AF: 0.203 AC: 429 AN: 2110

Alfa AF: 0.193 Hom.: 453

Bravo AF: 0.212

Asia WGS AF: 0.280 AC: 973 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	1.2
DANN	Benign	0.68
PhyloP100		-1.2
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: rs10497095; hg19: chr2-152977988;