6-11774350-A-G

Variant names:

• chr6-11774350-A-G
• rs6903956
• NM_032744.4:c.153+4257T>C

Variant summary

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

The NM_032744.4(ADTRP):​c.153+4257T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.651 in 151,694 control chromosomes in the GnomAD database, including 32,523 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 0.65 (32523 hom., cov: 29)
• Consequence: ADTRP NM_032744.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.16
• Publications: 58 publications found

Genes affected

ADTRP (HGNC:21214): (androgen dependent TFPI regulating protein) Enables hydrolase activity. Involved in several processes, including cell migration involved in sprouting angiogenesis; negative regulation of secretion by cell; and positive regulation of macromolecule metabolic process. Located in caveola and cell surface. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.91 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_032744.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ADTRP	NM_032744.4	MANE Select	c.153+4257T>C		intron	N/A	NP_116133.1
	ADTRP	NM_001143948.2		c.153+4257T>C		intron	N/A	NP_001137420.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ADTRP	ENST00000414691.8	TSL:1 MANE Select	c.153+4257T>C		intron	N/A	ENSP00000404416.2
	ADTRP	ENST00000229583.9	TSL:2	c.153+4257T>C		intron	N/A	ENSP00000229583.5
	ADTRP	ENST00000379415.6	TSL:5	c.153+4257T>C		intron	N/A	ENSP00000368726.2

Frequencies

GnomAD3 genomes AF: 0.651 AC: 98686 AN: 151578 Hom.: 32487 Cov.: 29

Gnomad AFR AF: 0.618

Gnomad AMI AF: 0.676

Gnomad AMR AF: 0.680

Gnomad ASJ AF: 0.630

Gnomad EAS AF: 0.932

Gnomad SAS AF: 0.806

Gnomad FIN AF: 0.688

Gnomad MID AF: 0.617

Gnomad NFE AF: 0.628

Gnomad OTH AF: 0.645

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

GnomAD4 genome AF: 0.651 AC: 98778 AN: 151694 Hom.: 32523 Cov.: 29 AF XY: 0.661 AC XY: 48990 AN XY: 74118

African (AFR) AF: 0.619 AC: 25552 AN: 41304

American (AMR) AF: 0.681 AC: 10385 AN: 15260

Ashkenazi Jewish (ASJ) AF: 0.630 AC: 2182 AN: 3466

East Asian (EAS) AF: 0.932 AC: 4803 AN: 5154

South Asian (SAS) AF: 0.805 AC: 3865 AN: 4800

European-Finnish (FIN) AF: 0.688 AC: 7207 AN: 10480

Middle Eastern (MID) AF: 0.616 AC: 180 AN: 292

European-Non Finnish (NFE) AF: 0.628 AC: 42623 AN: 67922

Other (OTH) AF: 0.649 AC: 1366 AN: 2106

Alfa AF: 0.636 Hom.: 139763

Bravo AF: 0.646

Asia WGS AF: 0.851 AC: 2955 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	7.2
DANN	Benign	0.76
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: rs6903956; hg19: chr6-11774583;