rs6655987

Variant names:

• chr1-167682750-G-A
• rs6655987
• NM_052862.4:c.7-1150G>A

Your query was ambiguous. Multiple possible variants found:

• chr1-167682750-G-A
• chr1-167682750-G-C
• chr1-167682750-G-T

Variant summary

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

The NM_052862.4(RCSD1):​c.7-1150G>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: 30)
• Consequence: RCSD1 NM_052862.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.174
• Publications: 0 publications found

Genes affected

RCSD1 (HGNC:28310): (RCSD domain containing 1) Enables actin filament binding activity. Involved in cellular hyperosmotic response. Predicted to be located in actin filament. [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=-0.89).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RCSD1	NM_052862.4	c.7-1150G>A		intron_variant	Intron 1 of 6	ENST00000367854.8	NP_443094.3
RCSD1	NM_001322923.2	c.7-1150G>A		intron_variant	Intron 1 of 5		NP_001309852.1
RCSD1	NM_001322924.2	c.7-1150G>A		intron_variant	Intron 1 of 4		NP_001309853.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RCSD1	ENST00000367854.8	c.7-1150G>A		intron_variant	Intron 1 of 6	1	NM_052862.4	ENSP00000356828.3
RCSD1	ENST00000537350.5	c.7-1150G>A		intron_variant	Intron 1 of 5	1		ENSP00000439409.1
RCSD1	ENST00000361496.3	c.7-1150G>A		intron_variant	Intron 1 of 4	3		ENSP00000355291.3

Frequencies

GnomAD3 genomes Cov.: 30

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

GnomAD4 genome Cov.: 30

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	1.3
DANN	Benign	0.64
PhyloP100		-0.17
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		0.98

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: rs6655987; hg19: chr1-167651987;