rs8135665

Variant names:

• chr22-38080269-C-T
• rs8135665
• NM_013356.3:c.1198+571G>A

Variant summary

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

The NM_013356.3(SLC16A8):​c.1198+571G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.24 in 152,032 control chromosomes in the GnomAD database, including 4,698 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as not provided (no stars).

• Frequency: Genomes: 𝑓 0.24 (4698 hom., cov: 32)
• Consequence: SLC16A8 NM_013356.3 intron
• Clinical Significance: not provided no classification provided O:1
• Conservation: PhyloP100: 0.689
• Publications: 74 publications found

Genes affected

SLC16A8 (HGNC:16270): (solute carrier family 16 member 8) SLC16A8 is a member of a family of proton-coupled monocarboxylate transporters that mediate lactate transport across cell membranes (Yoon et al., 1999 [PubMed 10493836]).[supplied by OMIM, Apr 2010]

LOC105373027 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.325 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_013356.3. 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
	SLC16A8	NM_013356.3	MANE Select	c.1198+571G>A		intron	N/A	NP_037488.2	O95907
	SLC16A8	NM_001394131.1		c.-80-1565G>A		intron	N/A	NP_001381060.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SLC16A8	ENST00000681075.2	MANE Select	c.1198+571G>A		intron	N/A	ENSP00000506669.1	O95907
	SLC16A8	ENST00000320521.10	TSL:1	c.1198+571G>A		intron	N/A	ENSP00000321735.5	O95907
	SLC16A8	ENST00000902580.1		c.1198+571G>A		intron	N/A	ENSP00000572639.1

Frequencies

GnomAD3 genomes AF: 0.240 AC: 36517 AN: 151914 Hom.: 4700 Cov.: 32

Gnomad AFR AF: 0.330

Gnomad AMI AF: 0.188

Gnomad AMR AF: 0.258

Gnomad ASJ AF: 0.215

Gnomad EAS AF: 0.132

Gnomad SAS AF: 0.196

Gnomad FIN AF: 0.221

Gnomad MID AF: 0.226

Gnomad NFE AF: 0.198

Gnomad OTH AF: 0.251

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

GnomAD4 genome AF: 0.240 AC: 36547 AN: 152032 Hom.: 4698 Cov.: 32 AF XY: 0.240 AC XY: 17816 AN XY: 74330

African (AFR) AF: 0.330 AC: 13665 AN: 41438

American (AMR) AF: 0.258 AC: 3938 AN: 15252

Ashkenazi Jewish (ASJ) AF: 0.215 AC: 747 AN: 3470

East Asian (EAS) AF: 0.132 AC: 686 AN: 5182

South Asian (SAS) AF: 0.197 AC: 952 AN: 4824

European-Finnish (FIN) AF: 0.221 AC: 2336 AN: 10584

Middle Eastern (MID) AF: 0.226 AC: 66 AN: 292

European-Non Finnish (NFE) AF: 0.198 AC: 13461 AN: 67968

Other (OTH) AF: 0.249 AC: 525 AN: 2110

Alfa AF: 0.214 Hom.: 13378

Bravo AF: 0.251

Asia WGS AF: 0.186 AC: 647 AN: 3478

ClinVar

ClinVar submissions

Significance: not provided

Revision: no classification provided

Pathogenic	VUS	Benign	Condition
-	-	-	not provided (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	13
DANN	Benign	0.68
PhyloP100		0.69
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.15		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: rs8135665; hg19: chr22-38476276;