rs61745585

Variant names:

• chr17-68271465-C-A
• rs61745585
• NM_004694.5:c.695G>T

Your query was ambiguous. Multiple possible variants found:

• chr17-68271465-C-A
• chr17-68271465-C-T

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_004694.5(SLC16A6):​c.695G>T​(p.Arg232Leu) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 15/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 32)
• Consequence: SLC16A6 NM_004694.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.53

Genes affected

SLC16A6 (HGNC:10927): (solute carrier family 16 member 6) Predicted to enable monocarboxylic acid transmembrane transporter activity. Predicted to be involved in monocarboxylic acid transport. Predicted to be located in membrane. Predicted to be integral component of plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ARSG (HGNC:24102): (arylsulfatase G) The protein encoded by this gene belongs to the sulfatase enzyme family. Sulfatases hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules. This protein displays arylsulfatase activity at acidic pH, as is typical of lysosomal sulfatases, and has been shown to localize in the lysosomes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.090895146).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SLC16A6	NM_004694.5	c.695G>T	p.Arg232Leu	missense_variant	Exon 5 of 6	ENST00000580666.6	NP_004685.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SLC16A6	ENST00000580666.6	c.695G>T	p.Arg232Leu	missense_variant	Exon 5 of 6	1	NM_004694.5	ENSP00000462985.1
SLC16A6	ENST00000327268.8	c.695G>T	p.Arg232Leu	missense_variant	Exon 6 of 7	1		ENSP00000319991.4
ARSG	ENST00000448504.6	c.-552+12039C>A		intron_variant	Intron 1 of 11	1		ENSP00000407193.2
ARSG	ENST00000578726.1	n.27-2425C>A		intron_variant	Intron 1 of 1	5

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.19
BayesDel_addAF	Benign	-0.26	T
BayesDel_noAF	Benign	-0.62
CADD	Benign	19
DANN	Benign	0.91
DEOGEN2	Benign	0.064	T;T;.
Eigen	Benign	-0.50
Eigen_PC	Benign	-0.40
FATHMM_MKL	Benign	0.18	N
LIST_S2	Uncertain	0.86	.;D;T
M_CAP	Benign	0.0034	T
MetaRNN	Benign	0.091	T;T;T
MetaSVM	Benign	-0.94	T
MutationAssessor	Benign	1.4	L;L;.
PrimateAI	Benign	0.35	T
PROVEAN	Benign	-0.92	N;.;.
REVEL	Benign	0.035
Sift	Benign	0.31	T;.;.
Sift4G	Benign	0.60	T;T;T
Polyphen		0.0060	B;B;.
Vest4		0.21
MutPred		0.57		Loss of catalytic residue at R232 (P = 0.0185);Loss of catalytic residue at R232 (P = 0.0185);Loss of catalytic residue at R232 (P = 0.0185);
MVP		0.27
MPC		0.58
ClinPred		0.096	T
GERP RS		2.4
Varity_R		0.13
gMVP		0.52

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

Publications

LitVar

Other links and lift over

dbSNP: rs61745585; hg19: chr17-66267606;