rs1320785944

Variant names:

• chr12-120534870-G-A
• rs1320785944
• NM_014868.5:c.59G>A

Your query was ambiguous. Multiple possible variants found:

• chr12-120534870-G-A
• chr12-120534870-G-C

Variant summary

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

The NM_001330474.2(RNF10):​c.59G>A​(p.Gly20Asp) variant causes a missense 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. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. G20A) has been classified as Uncertain significance.

• Frequency: Genomes: not found (cov: 32)
• Consequence: RNF10 NM_001330474.2 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 3.54
• Publications: 2 publications found

Genes affected

RNF10 (HGNC:10055): (ring finger protein 10) The protein encoded by this gene contains a ring finger motif, which is known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. EST data suggests the existence of multiple alternatively spliced transcript variants, however, their full length nature is not known. [provided by RefSeq, Jul 2008]

LOC128071547 (HGNC:0):

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 (MetaRNN=0.21507317).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001330474.2. 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
	RNF10	NM_014868.5	MANE Select	c.59G>A	p.Gly20Asp	missense	Exon 1 of 17	NP_055683.3
	LOC128071547	NM_001414895.1	MANE Select	c.174G>A	p.Arg58Arg	synonymous	Exon 1 of 1	NP_001401824.1
	RNF10	NM_001330474.2		c.59G>A	p.Gly20Asp	missense	Exon 1 of 17	NP_001317403.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RNF10	ENST00000325954.9	TSL:1 MANE Select	c.59G>A	p.Gly20Asp	missense	Exon 1 of 17	ENSP00000322242.4
	ENSG00000288623	ENST00000675818.1	MANE Select	c.174G>A	p.Arg58Arg	synonymous	Exon 1 of 1	ENSP00000502390.1
	RNF10	ENST00000413266.6	TSL:5	c.59G>A	p.Gly20Asp	missense	Exon 1 of 17	ENSP00000415682.2

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD2 exomes AF: 0.00 AC: 0 AN: 235518 AF XY: 0.00

Gnomad AFR exome AF: 0.00

Gnomad AMR exome AF: 0.00

Gnomad ASJ exome AF: 0.00

Gnomad EAS exome AF: 0.00

Gnomad FIN exome AF: 0.00

Gnomad NFE exome AF: 0.00

Gnomad OTH exome AF: 0.00

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.13
BayesDel_addAF	Uncertain	0.049	T
BayesDel_noAF	Benign	-0.17
CADD	Benign	22
DANN	Uncertain	0.99
DEOGEN2	Benign	0.019	T
Eigen	Benign	-0.31
Eigen_PC	Benign	-0.26
FATHMM_MKL	Uncertain	0.86	D
LIST_S2	Benign	0.83	T
M_CAP	Pathogenic	0.46	D
MetaRNN	Benign	0.22	T
MetaSVM	Uncertain	-0.10	T
MutationAssessor	Benign	-0.69	N
PhyloP100		3.5
PrimateAI	Uncertain	0.79	T
PROVEAN	Benign	-0.38	N
REVEL	Benign	0.28
Sift	Benign	0.17	T
Sift4G	Benign	0.92	T
Polyphen		0.91	P
Vest4		0.14
MutPred		0.15		Loss of glycosylation at S19 (P = 0.0308)
MVP		0.61
MPC		0.64
ClinPred		0.74	D
GERP RS		4.1
PromoterAI		0.097	Neutral
Varity_R		0.15
gMVP		0.17
Mutation Taster		=83/17	polymorphism

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: rs1320785944; hg19: chr12-120972673;