NM_001367551.1:c.312+1563A>T

Variant names:

• chr2-37185792-T-A
• rs11895771
• NM_001367551.1:c.312+1563A>T

Variant summary

Our verdict is Likely benign. Variant got -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001367551.1(SULT6B1):​c.312+1563A>T variant causes a intron 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. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 28)
• Consequence: SULT6B1 NM_001367551.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.729

Genes affected

SULT6B1 (HGNC:33433): (sulfotransferase family 6B member 1) Predicted to enable sulfotransferase activity. Predicted to be involved in sulfation. Predicted to be located in cytosol. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Likely_benign. Variant got -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SULT6B1	NM_001367551.1	c.312+1563A>T		intron_variant	Intron 2 of 6	ENST00000535679.6	NP_001354480.1
SULT6B1	NM_001032377.2	c.198+1563A>T		intron_variant	Intron 4 of 8		NP_001027549.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SULT6B1	ENST00000535679.6	c.312+1563A>T		intron_variant	Intron 2 of 6	1	NM_001367551.1	ENSP00000444081.1
SULT6B1	ENST00000407963.2	c.198+1563A>T		intron_variant	Intron 3 of 7	5		ENSP00000384950.1
SULT6B1	ENST00000689208.1	n.*82+1563A>T		intron_variant	Intron 2 of 6			ENSP00000510164.1
SULT6B1	ENST00000692190.1	n.198+1563A>T		intron_variant	Intron 2 of 6			ENSP00000509090.1

Frequencies

GnomAD3 genomes Cov.: 28

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

GnomAD4 genome Cov.: 28

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
CADD	Benign	3.9
DANN	Benign	0.39

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: rs11895771; hg19: chr2-37412935;