chr11-32186915-T-C

Variant names:

• chr11-32186915-T-C
• rs12577592
• ENST00000419556.2:n.292+43205A>G

Variant summary

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

The ENST00000419556.2(THEM7P):​n.292+43205A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.141 in 152,186 control chromosomes in the GnomAD database, including 1,721 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 0.14 (1721 hom., cov: 32)
• Consequence: THEM7P ENST00000419556.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 2.50
• Publications: 1 publications found

Genes affected

THEM7P (HGNC:50386): (thioesterase superfamily member 7, pseudogene)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.194 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000419556.2. 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
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	THEM7P	ENST00000419556.2	TSL:6	n.292+43205A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.141 AC: 21481 AN: 152066 Hom.: 1721 Cov.: 32

Gnomad AFR AF: 0.0526

Gnomad AMI AF: 0.0987

Gnomad AMR AF: 0.140

Gnomad ASJ AF: 0.249

Gnomad EAS AF: 0.196

Gnomad SAS AF: 0.203

Gnomad FIN AF: 0.147

Gnomad MID AF: 0.176

Gnomad NFE AF: 0.181

Gnomad OTH AF: 0.153

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

GnomAD4 genome AF: 0.141 AC: 21484 AN: 152186 Hom.: 1721 Cov.: 32 AF XY: 0.144 AC XY: 10727 AN XY: 74400

African (AFR) AF: 0.0525 AC: 2182 AN: 41544

American (AMR) AF: 0.139 AC: 2127 AN: 15268

Ashkenazi Jewish (ASJ) AF: 0.249 AC: 861 AN: 3460

East Asian (EAS) AF: 0.196 AC: 1014 AN: 5170

South Asian (SAS) AF: 0.204 AC: 986 AN: 4826

European-Finnish (FIN) AF: 0.147 AC: 1555 AN: 10586

Middle Eastern (MID) AF: 0.176 AC: 51 AN: 290

European-Non Finnish (NFE) AF: 0.181 AC: 12299 AN: 68020

Other (OTH) AF: 0.151 AC: 319 AN: 2110

Alfa AF: 0.162 Hom.: 747

Bravo AF: 0.134

Asia WGS AF: 0.183 AC: 635 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	7.3
DANN	Benign	0.66
PhyloP100		2.5

Splicing

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs12577592;

hg19: chr11-32208461;