rs2804918

Variant names:

• chr6-13584351-A-C
• rs2804918
• NM_012241.5:c.115+126A>C

Your query was ambiguous. Multiple possible variants found:

• chr6-13584351-A-C
• chr6-13584351-A-G
• chr6-13584351-A-T

Variant summary

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

The NM_012241.5(SIRT5):​c.115+126A>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: 31)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: SIRT5 NM_012241.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -3.00
• Publications: 7 publications found

Genes affected

SIRT5 (HGNC:14933): (sirtuin 5) This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class III of the sirtuin family. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2010]

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=-0.94).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_012241.5. 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
	SIRT5	NM_012241.5	MANE Select	c.115+126A>C		intron	N/A	NP_036373.1	Q9NXA8-1
	SIRT5	NM_001376798.1		c.115+126A>C		intron	N/A	NP_001363727.1	Q9NXA8-1
	SIRT5	NM_001376799.1		c.115+126A>C		intron	N/A	NP_001363728.1	Q9NXA8-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SIRT5	ENST00000606117.2	TSL:1 MANE Select	c.115+126A>C		intron	N/A	ENSP00000476228.1	Q9NXA8-1
	SIRT5	ENST00000397350.7	TSL:1	c.115+126A>C		intron	N/A	ENSP00000380509.3	Q9NXA8-1
	SIRT5	ENST00000379262.8	TSL:1	c.115+126A>C		intron	N/A	ENSP00000368564.4	Q9NXA8-2

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 515948 Hom.: 0 AF XY: 0.00 AC XY: 0 AN XY: 275814

African (AFR) AF: 0.00 AC: 0 AN: 13028

American (AMR) AF: 0.00 AC: 0 AN: 24318

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 16110

East Asian (EAS) AF: 0.00 AC: 0 AN: 31158

South Asian (SAS) AF: 0.00 AC: 0 AN: 50612

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 33408

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 3740

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 315316

Other (OTH) AF: 0.00 AC: 0 AN: 28258

GnomAD4 genome Cov.: 31

Alfa AF: 0.00 Hom.: 80885

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	0.41
DANN	Benign	0.67
PhyloP100		-3.0

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: rs2804918; hg19: chr6-13584583;