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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs398123088

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr17:7221006 (GRCh38.p13) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
T>C
Variation Type
SNV Single Nucleotide Variation
Frequency
None
Clinical Significance
Reported in ClinVar
Gene : Consequence
ACADVL : Missense Variant
DLG4 : 2KB Upstream Variant
Publications
1 citation
Genomic View
See rs on genome
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p13 chr 17 NC_000017.11:g.7221006T>C
GRCh37.p13 chr 17 NC_000017.10:g.7124325T>C
DLG4 RefSeqGene NG_008391.2:g.4045A>G
ACADVL RefSeqGene NG_007975.1:g.6173T>C
Gene: DLG4, discs large MAGUK scaffold protein 4 (minus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
DLG4 transcript variant 3 NM_001321074.1:c. N/A Upstream Transcript Variant
DLG4 transcript variant 1 NM_001365.4:c. N/A Upstream Transcript Variant
DLG4 transcript variant 2 NM_001128827.4:c. N/A N/A
DLG4 transcript variant 4 NM_001321075.3:c. N/A N/A
DLG4 transcript variant 5 NM_001321076.3:c. N/A N/A
DLG4 transcript variant 6 NM_001321077.3:c. N/A N/A
DLG4 transcript variant 8 NM_001369566.3:c. N/A N/A
DLG4 transcript variant 7 NR_135527.1:n. N/A Upstream Transcript Variant
DLG4 transcript variant X1 XM_011523699.2:c. N/A Upstream Transcript Variant
DLG4 transcript variant X2 XM_005256491.1:c. N/A N/A
DLG4 transcript variant X8 XM_011523702.1:c. N/A N/A
DLG4 transcript variant X4 XM_017024288.2:c. N/A N/A
DLG4 transcript variant X5 XM_017024289.2:c. N/A N/A
DLG4 transcript variant X3 XM_024450629.1:c. N/A N/A
DLG4 transcript variant X7 XR_934005.2:n. N/A Upstream Transcript Variant
Gene: ACADVL, acyl-CoA dehydrogenase very long chain (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ACADVL transcript variant 1 NM_000018.4:c.425T>C F [TTT] > S [TCT] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 1 precursor NP_000009.1:p.Phe142Ser F (Phe) > S (Ser) Missense Variant
ACADVL transcript variant 2 NM_001033859.3:c.359T>C F [TTT] > S [TCT] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 2 precursor NP_001029031.1:p.Phe120Ser F (Phe) > S (Ser) Missense Variant
ACADVL transcript variant 4 NM_001270448.2:c.197T>C F [TTT] > S [TCT] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 4 NP_001257377.1:p.Phe66Ser F (Phe) > S (Ser) Missense Variant
ACADVL transcript variant 3 NM_001270447.2:c.494T>C F [TTT] > S [TCT] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 3 NP_001257376.1:p.Phe165Ser F (Phe) > S (Ser) Missense Variant
ACADVL transcript variant X1 XM_006721516.3:c.425T>C F [TTT] > S [TCT] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X1 XP_006721579.2:p.Phe142Ser F (Phe) > S (Ser) Missense Variant
ACADVL transcript variant X2 XM_024450741.1:c.425T>C F [TTT] > S [TCT] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X2 XP_024306509.1:p.Phe142Ser F (Phe) > S (Ser) Missense Variant
ACADVL transcript variant X3 XM_011523829.2:c.425T>C F [TTT] > S [TCT] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X3 XP_011522131.1:p.Phe142Ser F (Phe) > S (Ser) Missense Variant
ACADVL transcript variant X4 XM_011523830.2:c.425T>C F [TTT] > S [TCT] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X4 XP_011522132.1:p.Phe142Ser F (Phe) > S (Ser) Missense Variant
ACADVL transcript variant X5 XR_934021.2:n.484T>C N/A Non Coding Transcript Variant
ACADVL transcript variant X6 XR_934022.2:n.484T>C N/A Non Coding Transcript Variant
ACADVL transcript variant X7 XR_934023.2:n.484T>C N/A Non Coding Transcript Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Allele: C (allele ID: 98194 )
ClinVar Accession Disease Names Clinical Significance
RCV000077916.4 not provided Uncertain-Significance
RCV000984921.2 Very long chain acyl-CoA dehydrogenase deficiency Likely-Pathogenic
Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

None
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement T= C
GRCh38.p13 chr 17 NC_000017.11:g.7221006= NC_000017.11:g.7221006T>C
GRCh37.p13 chr 17 NC_000017.10:g.7124325= NC_000017.10:g.7124325T>C
DLG4 RefSeqGene NG_008391.2:g.4045= NG_008391.2:g.4045A>G
ACADVL RefSeqGene NG_007975.1:g.6173= NG_007975.1:g.6173T>C
ACADVL transcript variant 1 NM_000018.4:c.425= NM_000018.4:c.425T>C
ACADVL transcript variant 1 NM_000018.3:c.425= NM_000018.3:c.425T>C
ACADVL transcript variant 2 NM_001033859.3:c.359= NM_001033859.3:c.359T>C
ACADVL transcript variant 2 NM_001033859.2:c.359= NM_001033859.2:c.359T>C
ACADVL transcript variant 4 NM_001270448.2:c.197= NM_001270448.2:c.197T>C
ACADVL transcript variant 4 NM_001270448.1:c.197= NM_001270448.1:c.197T>C
ACADVL transcript variant 3 NM_001270447.2:c.494= NM_001270447.2:c.494T>C
ACADVL transcript variant 3 NM_001270447.1:c.494= NM_001270447.1:c.494T>C
ACADVL transcript variant X1 XM_006721516.3:c.425= XM_006721516.3:c.425T>C
ACADVL transcript variant X5 XR_934021.2:n.484= XR_934021.2:n.484T>C
ACADVL transcript variant X7 XR_934023.2:n.484= XR_934023.2:n.484T>C
ACADVL transcript variant X3 XM_011523829.2:c.425= XM_011523829.2:c.425T>C
ACADVL transcript variant X6 XR_934022.2:n.484= XR_934022.2:n.484T>C
ACADVL transcript variant X4 XM_011523830.2:c.425= XM_011523830.2:c.425T>C
ACADVL transcript variant X2 XM_024450741.1:c.425= XM_024450741.1:c.425T>C
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 1 precursor NP_000009.1:p.Phe142= NP_000009.1:p.Phe142Ser
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 2 precursor NP_001029031.1:p.Phe120= NP_001029031.1:p.Phe120Ser
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 4 NP_001257377.1:p.Phe66= NP_001257377.1:p.Phe66Ser
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 3 NP_001257376.1:p.Phe165= NP_001257376.1:p.Phe165Ser
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X1 XP_006721579.2:p.Phe142= XP_006721579.2:p.Phe142Ser
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X3 XP_011522131.1:p.Phe142= XP_011522131.1:p.Phe142Ser
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X4 XP_011522132.1:p.Phe142= XP_011522132.1:p.Phe142Ser
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X2 XP_024306509.1:p.Phe142= XP_024306509.1:p.Phe142Ser
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

1 SubSNP, 2 ClinVar submissions
No Submitter Submission ID Date (Build)
1 EGL ss947846743 Jan 23, 2014 (138)
2 ClinVar RCV000077916.4 Oct 12, 2018 (152)
3 ClinVar RCV000984921.2 Apr 27, 2021 (155)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
RCV000077916.4, RCV000984921.2, ss947846743 NC_000017.11:7221005:T:C NC_000017.11:7221005:T:C (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

1 citation for rs398123088
PMID Title Author Year Journal
23757202 Free the data: one laboratory's approach to knowledge-based genomic variant classification and preparation for EMR integration of genomic data. Bean LJ et al. 2013 Human mutation
Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post596+ae089ad