rs1563634

Variant names:

• chr17-18315490-T-A
• rs1563634
• NM_144775.3:c.-300T>A

Your query was ambiguous. Multiple possible variants found:

• chr17-18315490-T-A
• chr17-18315490-T-C
• chr17-18315490-T-G

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_144775.3(SMCR8):​c.-300T>A variant causes a 5 prime UTR 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: 34)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: SMCR8 NM_144775.3 5_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.581
• Publications: 11 publications found

Genes affected

SMCR8 (HGNC:17921): (SMCR8-C9orf72 complex subunit) Enables protein kinase binding activity and protein kinase inhibitor activity. Contributes to guanyl-nucleotide exchange factor activity. Involved in negative regulation of macromolecule metabolic process; regulation of TOR signaling; and regulation of macroautophagy. Located in chromatin; cytoplasm; and nucleoplasm. Part of guanyl-nucleotide exchange factor complex. Colocalizes with Atg1/ULK1 kinase complex. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.38).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SMCR8	NM_144775.3	c.-300T>A		5_prime_UTR_variant	Exon 1 of 2	ENST00000406438.5	NP_658988.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SMCR8	ENST00000406438.5	c.-300T>A		5_prime_UTR_variant	Exon 1 of 2	1	NM_144775.3	ENSP00000385025.3

Frequencies

GnomAD3 genomes Cov.: 34

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 182186 Hom.: 0 Cov.: 1 AF XY: 0.00 AC XY: 0 AN XY: 93724

African (AFR) AF: 0.00 AC: 0 AN: 6068

American (AMR) AF: 0.00 AC: 0 AN: 6854

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 6000

East Asian (EAS) AF: 0.00 AC: 0 AN: 12386

South Asian (SAS) AF: 0.00 AC: 0 AN: 15356

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 9424

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 844

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 113968

Other (OTH) AF: 0.00 AC: 0 AN: 11286

GnomAD4 genome Cov.: 34

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.38
CADD	Benign	15
DANN	Benign	0.77
PhyloP100		0.58
PromoterAI		0.015	Neutral
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.0

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

Other links and lift over

dbSNP: rs1563634; hg19: chr17-18218804;