rs10493147

Variant names:

• chr4-127816344-T-A
• rs10493147
• NM_014278.4:c.1579-1981T>A

Your query was ambiguous. Multiple possible variants found:

• chr4-127816344-T-A
• chr4-127816344-T-C

Variant summary

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

The NM_014278.4(HSPA4L):​c.1579-1981T>A 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: 32)
• Consequence: HSPA4L NM_014278.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.642
• Publications: 10 publications found

Genes affected

HSPA4L (HGNC:17041): (heat shock protein family A (Hsp70) member 4 like) The protein encoded by this gene is heat shock inducible and may act as a chaperone. The encoded protein can protect the heat-shocked cell against the harmful effects of aggregated proteins. This gene is highly expressed in leukemia cells and may be a good target for therapeutic intervention. Several transcripts encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]

ENSG00000295993 (HGNC:58883):

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_014278.4. 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
	HSPA4L	NM_014278.4	MANE Select	c.1579-1981T>A		intron	N/A	NP_055093.2
	HSPA4L	NM_001317381.2		c.1672-1981T>A		intron	N/A	NP_001304310.1
	HSPA4L	NM_001317382.2		c.1501-1981T>A		intron	N/A	NP_001304311.1	E9PDE8

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	HSPA4L	ENST00000296464.9	TSL:1 MANE Select	c.1579-1981T>A		intron	N/A	ENSP00000296464.3	O95757
	HSPA4L	ENST00000508549.5	TSL:1	c.1456-1981T>A		intron	N/A	ENSP00000427305.1	D6RJ96
	HSPA4L	ENST00000508776.5	TSL:2	c.1579-1981T>A		intron	N/A	ENSP00000422482.1	O95757

Frequencies

GnomAD3 genomes Cov.: 32

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

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	0.82
DANN	Benign	0.66
PhyloP100		-0.64

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: rs10493147; hg19: chr4-128737499;