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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.


Current Build 154

Released April 21, 2020

Homo sapiens
chr8:18400414 (GRCh38.p12) 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.

A>C / A>T
Variation Type
SNV Single Nucleotide Variation
C=0.000004 (1/248606, GnomAD_exome)
C=0.000008 (1/120656, ExAC)
T=0.000 (0/328, HapMap) (+ 1 more)
C=0.0 (0/10680, ALFA Project)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
NAT2 : Missense Variant
1 citation
Genomic View
See rs on genome

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.p12 chr 8 NC_000008.11:g.18400414A>C
GRCh38.p12 chr 8 NC_000008.11:g.18400414A>T
GRCh37.p13 chr 8 NC_000008.10:g.18257924A>C
GRCh37.p13 chr 8 NC_000008.10:g.18257924A>T
NAT2 RefSeqGene NG_012246.1:g.14170A>C
NAT2 RefSeqGene NG_012246.1:g.14170A>T
Gene: NAT2, N-acetyltransferase 2 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
NAT2 transcript NM_000015.3:c.411A>C L [TTA] > F [TTC] Coding Sequence Variant
arylamine N-acetyltransferase 2 NP_000006.2:p.Leu137Phe L (Leu) > F (Phe) Missense Variant
NAT2 transcript NM_000015.3:c.411A>T L [TTA] > F [TTT] Coding Sequence Variant
arylamine N-acetyltransferase 2 NP_000006.2:p.Leu137Phe L (Leu) > F (Phe) Missense Variant
NAT2 transcript variant X1 XM_017012938.1:c.411A>C L [TTA] > F [TTC] Coding Sequence Variant
arylamine N-acetyltransferase 2 isoform X1 XP_016868427.1:p.Leu137Phe L (Leu) > F (Phe) Missense Variant
NAT2 transcript variant X1 XM_017012938.1:c.411A>T L [TTA] > F [TTT] Coding Sequence Variant
arylamine N-acetyltransferase 2 isoform X1 XP_016868427.1:p.Leu137Phe L (Leu) > F (Phe) Missense Variant

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

ALFA Allele Frequency (New)
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 10680 A=1.00000 C=0.00000
European Sub 6962 A=1.0000 C=0.0000
African Sub 2294 A=1.0000 C=0.0000
African Others Sub 84 A=1.00 C=0.00
African American Sub 2210 A=1.0000 C=0.0000
Asian Sub 108 A=1.000 C=0.000
East Asian Sub 84 A=1.00 C=0.00
Other Asian Sub 24 A=1.00 C=0.00
Latin American 1 Sub 146 A=1.000 C=0.000
Latin American 2 Sub 610 A=1.000 C=0.000
South Asian Sub 94 A=1.00 C=0.00
Other Sub 466 A=1.000 C=0.000


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").

Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Exomes Global Study-wide 248606 A=0.999996 C=0.000004
gnomAD - Exomes European Sub 134228 A=0.999993 C=0.000007
gnomAD - Exomes Asian Sub 48378 A=1.00000 C=0.00000
gnomAD - Exomes American Sub 33998 A=1.00000 C=0.00000
gnomAD - Exomes African Sub 16196 A=1.00000 C=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 9786 A=1.0000 C=0.0000
gnomAD - Exomes Other Sub 6020 A=1.0000 C=0.0000
ExAC Global Study-wide 120656 A=0.999992 C=0.000008
ExAC Europe Sub 73064 A=0.99999 C=0.00001
ExAC Asian Sub 24842 A=1.00000 C=0.00000
ExAC American Sub 11496 A=1.00000 C=0.00000
ExAC African Sub 10352 A=1.00000 C=0.00000
ExAC Other Sub 902 A=1.000 C=0.000
HapMap Global Study-wide 328 A=1.000 T=0.000
HapMap African Sub 120 A=1.000 T=0.000
HapMap American Sub 120 A=1.000 T=0.000
HapMap Asian Sub 88 A=1.00 T=0.00

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 T
GRCh38.p12 chr 8 NC_000008.11:g.18400414= NC_000008.11:g.18400414A>C NC_000008.11:g.18400414A>T
GRCh37.p13 chr 8 NC_000008.10:g.18257924= NC_000008.10:g.18257924A>C NC_000008.10:g.18257924A>T
NAT2 RefSeqGene NG_012246.1:g.14170= NG_012246.1:g.14170A>C NG_012246.1:g.14170A>T
NAT2 transcript NM_000015.3:c.411= NM_000015.3:c.411A>C NM_000015.3:c.411A>T
NAT2 transcript NM_000015.2:c.411= NM_000015.2:c.411A>C NM_000015.2:c.411A>T
NAT2 transcript variant X1 XM_017012938.1:c.411= XM_017012938.1:c.411A>C XM_017012938.1:c.411A>T
arylamine N-acetyltransferase 2 NP_000006.2:p.Leu137= NP_000006.2:p.Leu137Phe NP_000006.2:p.Leu137Phe
arylamine N-acetyltransferase 2 isoform X1 XP_016868427.1:p.Leu137= XP_016868427.1:p.Leu137Phe XP_016868427.1:p.Leu137Phe

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#.

4 SubSNP, 3 Frequency submissions
No Submitter Submission ID Date (Build)
1 SNP500CANCER ss5586802 Mar 31, 2003 (113)
2 EVA_EXAC ss1689107856 Apr 01, 2015 (144)
3 ILLUMINA ss2711131670 Nov 08, 2017 (151)
4 GNOMAD ss2737016682 Nov 08, 2017 (151)
5 ExAC NC_000008.10 - 18257924 Oct 12, 2018 (152)
6 gnomAD - Exomes NC_000008.10 - 18257924 Jul 13, 2019 (153)
7 HapMap NC_000008.11 - 18400414 Apr 26, 2020 (154)

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
9201214, 6184621, ss1689107856, ss2737016682 NC_000008.10:18257923:A:C NC_000008.11:18400413:A:C (self)
ss2711131670 NC_000008.10:18257923:A:T NC_000008.11:18400413:A:T (self)
3577448 NC_000008.11:18400413:A:T NC_000008.11:18400413:A:T
ss5586802 NT_167187.1:6116069:A:T NC_000008.11:18400413:A:T (self)

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

1 citation for rs4986997
PMID Title Author Year Journal
18680467 Structure/function evaluations of single nucleotide polymorphisms in human N-acetyltransferase 2. Walraven JM et al. 2008 Current drug metabolism

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.post557+f76c771