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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.

rs772299277

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:231818378 (GRCh38.p14) 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
A>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.000008 (2/251238, GnomAD_exome)
C=0.000016 (2/121362, ExAC)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
DISC1 : Missense Variant
TSNAX-DISC1 : Non Coding Transcript Variant
DISC2 : Non Coding Transcript Variant (+ 1 more)
LOC105373170 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome
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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Exomes Global Study-wide 251238 A=0.999992 C=0.000008
gnomAD - Exomes European Sub 135202 A=0.999993 C=0.000007
gnomAD - Exomes Asian Sub 49002 A=1.00000 C=0.00000
gnomAD - Exomes American Sub 34572 A=1.00000 C=0.00000
gnomAD - Exomes African Sub 16256 A=1.00000 C=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10072 A=1.00000 C=0.00000
gnomAD - Exomes Other Sub 6134 A=0.9998 C=0.0002
ExAC Global Study-wide 121362 A=0.999984 C=0.000016
ExAC Europe Sub 73344 A=0.99999 C=0.00001
ExAC Asian Sub 25156 A=1.00000 C=0.00000
ExAC American Sub 11548 A=1.00000 C=0.00000
ExAC African Sub 10406 A=1.00000 C=0.00000
ExAC Other Sub 908 A=0.999 C=0.001
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.p14 chr 1 NC_000001.11:g.231818378A>C
GRCh37.p13 chr 1 NC_000001.10:g.231954124A>C
DISC1 RefSeqGene NG_011681.2:g.196564A>C
Gene: DISC1, DISC1 scaffold protein (plus strand)
Molecule type Change Amino acid[Codon] SO Term
DISC1 transcript variant h NM_001164545.2:c.1739A>C * [TAA] > S [TCA] Terminator Codon Variant
disrupted in schizophrenia 1 protein isoform h NP_001158017.1:p.Ter580Ser * (Ter) > S (Ser) Stop Lost
DISC1 transcript variant i NM_001164546.2:c.1634+473…

NM_001164546.2:c.1634+47308A>C

N/A Intron Variant
DISC1 transcript variant j NM_001164547.2:c.1634+473…

NM_001164547.2:c.1634+47308A>C

N/A Intron Variant
DISC1 transcript variant k NM_001164548.2:c.*28= N/A 3 Prime UTR Variant
DISC1 transcript variant t NM_001164556.2:c.*28= N/A 3 Prime UTR Variant
DISC1 transcript variant Es NM_001012958.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant l NM_001164549.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant m NM_001164550.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant n NM_001164551.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant o NM_001164552.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant p NM_001164553.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant q NM_001164554.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant r NM_001164555.2:c. N/A Genic Downstream Transcript Variant
DISC1 transcript variant b NM_001164538.2:c.1842A>C L [TTA] > F [TTC] Coding Sequence Variant
disrupted in schizophrenia 1 protein isoform b NP_001158010.1:p.Leu614Phe L (Leu) > F (Phe) Missense Variant
DISC1 transcript variant d NM_001164540.2:c.1476A>C L [TTA] > F [TTC] Coding Sequence Variant
disrupted in schizophrenia 1 protein isoform d NP_001158012.1:p.Leu492Phe L (Leu) > F (Phe) Missense Variant
DISC1 transcript variant S NM_001012959.2:c.1842A>C L [TTA] > F [TTC] Coding Sequence Variant
disrupted in schizophrenia 1 protein isoform S NP_001012977.1:p.Leu614Phe L (Leu) > F (Phe) Missense Variant
DISC1 transcript variant f NM_001164542.2:c.1842A>C L [TTA] > F [TTC] Coding Sequence Variant
disrupted in schizophrenia 1 protein isoform f NP_001158014.1:p.Leu614Phe L (Leu) > F (Phe) Missense Variant
DISC1 transcript variant L NM_018662.3:c.1842A>C L [TTA] > F [TTC] Coding Sequence Variant
disrupted in schizophrenia 1 protein isoform L NP_061132.2:p.Leu614Phe L (Leu) > F (Phe) Missense Variant
DISC1 transcript variant c NM_001164539.2:c.1842A>C L [TTA] > F [TTC] Coding Sequence Variant
disrupted in schizophrenia 1 protein isoform c NP_001158011.1:p.Leu614Phe L (Leu) > F (Phe) Missense Variant
DISC1 transcript variant e NM_001164541.2:c.1842A>C L [TTA] > F [TTC] Coding Sequence Variant
disrupted in schizophrenia 1 protein isoform e NP_001158013.1:p.Leu614Phe L (Leu) > F (Phe) Missense Variant
DISC1 transcript variant a NM_001164537.2:c.1938A>C L [TTA] > F [TTC] Coding Sequence Variant
disrupted in schizophrenia 1 protein isoform a NP_001158009.1:p.Leu646Phe L (Leu) > F (Phe) Missense Variant
DISC1 transcript variant Lv NM_001012957.2:c.1842A>C L [TTA] > F [TTC] Coding Sequence Variant
disrupted in schizophrenia 1 protein isoform Lv NP_001012975.1:p.Leu614Phe L (Leu) > F (Phe) Missense Variant
DISC1 transcript variant g NM_001164544.2:c.1842A>C L [TTA] > F [TTC] Coding Sequence Variant
disrupted in schizophrenia 1 protein isoform g NP_001158016.1:p.Leu614Phe L (Leu) > F (Phe) Missense Variant
Gene: DISC2, disrupted in schizophrenia 2 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
DISC2 transcript NR_002227.2:n.140T>G N/A Non Coding Transcript Variant
Gene: TSNAX-DISC1, TSNAX-DISC1 readthrough (NMD candidate) (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TSNAX-DISC1 transcript variant 1 NR_028393.1:n.2508A>C N/A Non Coding Transcript Variant
TSNAX-DISC1 transcript variant 2 NR_028394.1:n.2691A>C N/A Non Coding Transcript Variant
TSNAX-DISC1 transcript variant 3 NR_028395.1:n.2588A>C N/A Non Coding Transcript Variant
TSNAX-DISC1 transcript variant 5 NR_028397.1:n.2428A>C N/A Non Coding Transcript Variant
TSNAX-DISC1 transcript variant 4 NR_028396.1:n.2563A>C N/A Non Coding Transcript Variant
TSNAX-DISC1 transcript variant 6 NR_028398.1:n.2182A>C N/A Non Coding Transcript Variant
TSNAX-DISC1 transcript variant 7 NR_028399.1:n. N/A Genic Downstream Transcript Variant
TSNAX-DISC1 transcript variant 8 NR_028400.1:n. N/A Genic Downstream Transcript Variant
Gene: LOC105373170, uncharacterized LOC105373170 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
LOC105373170 transcript variant X4 XR_001738521.2:n. N/A Intron Variant
LOC105373170 transcript variant X1 XR_007066940.1:n. N/A Intron Variant
LOC105373170 transcript variant X2 XR_949268.4:n. N/A Intron Variant
LOC105373170 transcript variant X3 XR_949269.3:n. N/A Intron 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.

Not Reported in ClinVar
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 A= C
GRCh38.p14 chr 1 NC_000001.11:g.231818378= NC_000001.11:g.231818378A>C
GRCh37.p13 chr 1 NC_000001.10:g.231954124= NC_000001.10:g.231954124A>C
DISC1 RefSeqGene NG_011681.2:g.196564= NG_011681.2:g.196564A>C
DISC1 transcript variant L NM_018662.3:c.1842= NM_018662.3:c.1842A>C
DISC1 transcript variant L NM_018662.2:c.1842= NM_018662.2:c.1842A>C
DISC1 transcript variant a NM_001164537.2:c.1938= NM_001164537.2:c.1938A>C
DISC1 transcript variant a NM_001164537.1:c.1938= NM_001164537.1:c.1938A>C
DISC1 transcript variant Lv NM_001012957.2:c.1842= NM_001012957.2:c.1842A>C
DISC1 transcript variant Lv NM_001012957.1:c.1842= NM_001012957.1:c.1842A>C
DISC1 transcript variant d NM_001164540.2:c.1476= NM_001164540.2:c.1476A>C
DISC1 transcript variant d NM_001164540.1:c.1476= NM_001164540.1:c.1476A>C
DISC1 transcript variant b NM_001164538.2:c.1842= NM_001164538.2:c.1842A>C
DISC1 transcript variant b NM_001164538.1:c.1842= NM_001164538.1:c.1842A>C
DISC1 transcript variant e NM_001164541.2:c.1842= NM_001164541.2:c.1842A>C
DISC1 transcript variant e NM_001164541.1:c.1842= NM_001164541.1:c.1842A>C
DISC1 transcript variant g NM_001164544.2:c.1842= NM_001164544.2:c.1842A>C
DISC1 transcript variant g NM_001164544.1:c.1842= NM_001164544.1:c.1842A>C
DISC1 transcript variant f NM_001164542.2:c.1842= NM_001164542.2:c.1842A>C
DISC1 transcript variant f NM_001164542.1:c.1842= NM_001164542.1:c.1842A>C
DISC1 transcript variant c NM_001164539.2:c.1842= NM_001164539.2:c.1842A>C
DISC1 transcript variant c NM_001164539.1:c.1842= NM_001164539.1:c.1842A>C
DISC1 transcript variant h NM_001164545.2:c.1739= NM_001164545.2:c.1739A>C
DISC1 transcript variant h NM_001164545.1:c.1739= NM_001164545.1:c.1739A>C
DISC1 transcript variant k NM_001164548.2:c.*28= NM_001164548.2:c.*28A>C
DISC1 transcript variant k NM_001164548.1:c.*28= NM_001164548.1:c.*28A>C
DISC1 transcript variant S NM_001012959.2:c.1842= NM_001012959.2:c.1842A>C
DISC1 transcript variant S NM_001012959.1:c.1842= NM_001012959.1:c.1842A>C
DISC1 transcript variant t NM_001164556.2:c.*28= NM_001164556.2:c.*28A>C
DISC1 transcript variant t NM_001164556.1:c.*28= NM_001164556.1:c.*28A>C
DISC2 transcript NR_002227.2:n.140= NR_002227.2:n.140T>G
TSNAX-DISC1 transcript variant 1 NR_028393.1:n.2508= NR_028393.1:n.2508A>C
TSNAX-DISC1 transcript variant 2 NR_028394.1:n.2691= NR_028394.1:n.2691A>C
TSNAX-DISC1 transcript variant 3 NR_028395.1:n.2588= NR_028395.1:n.2588A>C
TSNAX-DISC1 transcript variant 4 NR_028396.1:n.2563= NR_028396.1:n.2563A>C
TSNAX-DISC1 transcript variant 5 NR_028397.1:n.2428= NR_028397.1:n.2428A>C
TSNAX-DISC1 transcript variant 6 NR_028398.1:n.2182= NR_028398.1:n.2182A>C
disrupted in schizophrenia 1 protein isoform L NP_061132.2:p.Leu614= NP_061132.2:p.Leu614Phe
disrupted in schizophrenia 1 protein isoform a NP_001158009.1:p.Leu646= NP_001158009.1:p.Leu646Phe
disrupted in schizophrenia 1 protein isoform Lv NP_001012975.1:p.Leu614= NP_001012975.1:p.Leu614Phe
disrupted in schizophrenia 1 protein isoform d NP_001158012.1:p.Leu492= NP_001158012.1:p.Leu492Phe
disrupted in schizophrenia 1 protein isoform b NP_001158010.1:p.Leu614= NP_001158010.1:p.Leu614Phe
disrupted in schizophrenia 1 protein isoform e NP_001158013.1:p.Leu614= NP_001158013.1:p.Leu614Phe
disrupted in schizophrenia 1 protein isoform g NP_001158016.1:p.Leu614= NP_001158016.1:p.Leu614Phe
disrupted in schizophrenia 1 protein isoform f NP_001158014.1:p.Leu614= NP_001158014.1:p.Leu614Phe
disrupted in schizophrenia 1 protein isoform c NP_001158011.1:p.Leu614= NP_001158011.1:p.Leu614Phe
disrupted in schizophrenia 1 protein isoform h NP_001158017.1:p.Ter580= NP_001158017.1:p.Ter580Ser
disrupted in schizophrenia 1 protein isoform S NP_001012977.1:p.Leu614= NP_001012977.1:p.Leu614Phe
DISC1 transcript variant i NM_001164546.1:c.1634+47308= NM_001164546.1:c.1634+47308A>C
DISC1 transcript variant i NM_001164546.2:c.1634+47308= NM_001164546.2:c.1634+47308A>C
DISC1 transcript variant j NM_001164547.1:c.1634+47308= NM_001164547.1:c.1634+47308A>C
DISC1 transcript variant j NM_001164547.2:c.1634+47308= NM_001164547.2:c.1634+47308A>C
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#.

2 SubSNP, 2 Frequency submissions
No Submitter Submission ID Date (Build)
1 EVA_EXAC ss1686111549 Apr 01, 2015 (144)
2 GNOMAD ss2732363037 Nov 08, 2017 (151)
3 ExAC NC_000001.10 - 231954124 Oct 11, 2018 (152)
4 gnomAD - Exomes NC_000001.10 - 231954124 Jul 12, 2019 (153)
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
5352235, 1400809, ss1686111549, ss2732363037 NC_000001.10:231954123:A:C NC_000001.11:231818377:A:C (self)
Help

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

No publications for rs772299277

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.post761+d5e8e07