rs4674015

Variant names:

• chr2-200389448-A-C
• rs4674015
• NM_001100423.2:c.39+165A>C

Your query was ambiguous. Multiple possible variants found:

• chr2-200389448-A-C
• chr2-200389448-A-G
• chr2-200389448-A-T

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001100423.2(SPATS2L):​c.39+165A>C 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: 33)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: SPATS2L NM_001100423.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.480
• Publications: 5 publications found

Genes affected

SPATS2L (HGNC:24574): (spermatogenesis associated serine rich 2 like) Enables RNA binding activity. Located in cytosol; nucleolus; and nucleoplasm. Part of protein-containing complex. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001100423.2. 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
	SPATS2L	NM_001100423.2	MANE Select	c.39+165A>C		intron	N/A	NP_001093893.1	Q9NUQ6-1
	SPATS2L	NM_001282744.2		c.129+165A>C		intron	N/A	NP_001269673.1	Q9NUQ6-3
	SPATS2L	NM_001100422.1		c.39+165A>C		intron	N/A	NP_001093892.1	Q9NUQ6-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SPATS2L	ENST00000409140.8	TSL:2 MANE Select	c.39+165A>C		intron	N/A	ENSP00000386730.3	Q9NUQ6-1
	SPATS2L	ENST00000358677.9	TSL:1	c.39+165A>C		intron	N/A	ENSP00000351503.4	Q9NUQ6-1
	SPATS2L	ENST00000360760.9	TSL:1	c.39+165A>C		intron	N/A	ENSP00000353989.5	Q9NUQ6-2

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Data not reliable, filtered out with message: AC0;AS_VQSR AF: 0.00 AC: 0 AN: 382232 Hom.: 0 Cov.: 4 AF XY: 0.00 AC XY: 0 AN XY: 200544

African (AFR) AF: 0.00 AC: 0 AN: 10932

American (AMR) AF: 0.00 AC: 0 AN: 13040

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 12056

East Asian (EAS) AF: 0.00 AC: 0 AN: 28190

South Asian (SAS) AF: 0.00 AC: 0 AN: 29416

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 30662

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 3344

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 232014

Other (OTH) AF: 0.00 AC: 0 AN: 22578

GnomAD4 genome Cov.: 33

Alfa AF: 0.00 Hom.: 51740

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	0.12
DANN	Benign	0.41
PhyloP100		-0.48

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: rs4674015; hg19: chr2-201254171;