chr8-118792647-G-A

Variant names:

• chr8-118792647-G-A
• rs10955900
• ENST00000625758.3:n.1320+28263G>A

Variant summary

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

The ENST00000625758.3(SAMD12-AS1):​n.1320+28263G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.336 in 151,882 control chromosomes in the GnomAD database, including 10,349 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 0.34 (10349 hom., cov: 32)
• Consequence: SAMD12-AS1 ENST00000625758.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0540
• Publications: 1 publications found

Genes affected

SAMD12-AS1 (HGNC:30937): (SAMD12 antisense RNA 1)

ENSG00000306504 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.6).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.456 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000625758.3. 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
There are no transcript annotations for this variant.

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SAMD12-AS1	ENST00000625758.3	TSL:5	n.1320+28263G>A		intron	N/A
	SAMD12-AS1	ENST00000629661.1	TSL:5	n.496-65410G>A		intron	N/A
	SAMD12-AS1	ENST00000658340.1		n.900+28263G>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.336 AC: 51023 AN: 151764 Hom.: 10345 Cov.: 32

Gnomad AFR AF: 0.119

Gnomad AMI AF: 0.609

Gnomad AMR AF: 0.379

Gnomad ASJ AF: 0.344

Gnomad EAS AF: 0.125

Gnomad SAS AF: 0.240

Gnomad FIN AF: 0.444

Gnomad MID AF: 0.297

Gnomad NFE AF: 0.461

Gnomad OTH AF: 0.362

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

GnomAD4 genome AF: 0.336 AC: 51036 AN: 151882 Hom.: 10349 Cov.: 32 AF XY: 0.333 AC XY: 24716 AN XY: 74212

African (AFR) AF: 0.119 AC: 4922 AN: 41458

American (AMR) AF: 0.380 AC: 5786 AN: 15240

Ashkenazi Jewish (ASJ) AF: 0.344 AC: 1193 AN: 3464

East Asian (EAS) AF: 0.124 AC: 644 AN: 5174

South Asian (SAS) AF: 0.241 AC: 1160 AN: 4822

European-Finnish (FIN) AF: 0.444 AC: 4677 AN: 10536

Middle Eastern (MID) AF: 0.299 AC: 88 AN: 294

European-Non Finnish (NFE) AF: 0.460 AC: 31253 AN: 67868

Other (OTH) AF: 0.359 AC: 759 AN: 2116

Alfa AF: 0.400 Hom.: 1674

Bravo AF: 0.325

Asia WGS AF: 0.187 AC: 652 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.60
CADD	Benign	7.5
DANN	Benign	0.78
PhyloP100		0.054

Splicing

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

Other links and lift over

dbSNP: rs10955900; hg19: chr8-119804886;