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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs1455266125

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr11:8436089 (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
T>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.000004 (1/264690, TOPMED)
C=0.000007 (1/140264, GnomAD)
C=0.00000 (0/14050, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
STK33 : Missense Variant
Publications
0 citations
Genomic View
See rs on genome

ALFA Allele Frequency
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: 20231103111315
Population Group Sample Size Ref Allele Alt Allele Ref HMOZ Alt HMOZ HTRZ HWEP
Total Global 14050 T=1.00000 C=0.00000 1.0 0.0 0.0 N/A
European Sub 9690 T=1.0000 C=0.0000 1.0 0.0 0.0 N/A
African Sub 2898 T=1.0000 C=0.0000 1.0 0.0 0.0 N/A
African Others Sub 114 T=1.000 C=0.000 1.0 0.0 0.0 N/A
African American Sub 2784 T=1.0000 C=0.0000 1.0 0.0 0.0 N/A
Asian Sub 112 T=1.000 C=0.000 1.0 0.0 0.0 N/A
East Asian Sub 86 T=1.00 C=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 26 T=1.00 C=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 T=1.000 C=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 T=1.000 C=0.000 1.0 0.0 0.0 N/A
South Asian Sub 98 T=1.00 C=0.00 1.0 0.0 0.0 N/A
Other Sub 496 T=1.000 C=0.000 1.0 0.0 0.0 N/A


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
TopMed Global Study-wide 264690 T=0.999996 C=0.000004
gnomAD - Genomes Global Study-wide 140264 T=0.999993 C=0.000007
gnomAD - Genomes European Sub 75952 T=1.00000 C=0.00000
gnomAD - Genomes African Sub 42044 T=1.00000 C=0.00000
gnomAD - Genomes American Sub 13664 T=1.00000 C=0.00000
gnomAD - Genomes Ashkenazi Jewish Sub 3318 T=1.0000 C=0.0000
gnomAD - Genomes East Asian Sub 3134 T=0.9997 C=0.0003
gnomAD - Genomes Other Sub 2152 T=1.0000 C=0.0000
Allele Frequency Aggregator Total Global 14050 T=1.00000 C=0.00000
Allele Frequency Aggregator European Sub 9690 T=1.0000 C=0.0000
Allele Frequency Aggregator African Sub 2898 T=1.0000 C=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 T=1.000 C=0.000
Allele Frequency Aggregator Other Sub 496 T=1.000 C=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 T=1.000 C=0.000
Allele Frequency Aggregator Asian Sub 112 T=1.000 C=0.000
Allele Frequency Aggregator South Asian Sub 98 T=1.00 C=0.00
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 11 NC_000011.10:g.8436089T>C
GRCh37.p13 chr 11 NC_000011.9:g.8457636T>C
Gene: STK33, serine/threonine kinase 33 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
STK33 transcript variant 3 NM_001289059.2:c.437A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform c NP_001275988.1:p.Glu146Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 1 NM_030906.4:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform a NP_112168.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 7 NM_001352389.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform a NP_001339318.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 17 NM_001352399.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform e NP_001339328.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 9 NM_001352391.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform a NP_001339320.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 15 NM_001352397.2:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform d NP_001339326.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 11 NM_001352393.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform a NP_001339322.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 2 NM_001289058.2:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform b NP_001275987.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 6 NM_001352388.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform a NP_001339317.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 8 NM_001352390.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform a NP_001339319.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 12 NM_001352394.2:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform b NP_001339323.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 10 NM_001352392.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform a NP_001339321.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 13 NM_001352395.2:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform b NP_001339324.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 5 NM_001352387.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform a NP_001339316.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 16 NM_001352398.2:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform d NP_001339327.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 14 NM_001352396.2:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform d NP_001339325.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant 4 NM_001289061.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform a NP_001275990.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X1 XM_017018146.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_016873635.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X2 XM_047427447.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283403.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X3 XM_017018145.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_016873634.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X4 XM_047427448.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283404.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X5 XM_047427449.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283405.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X6 XM_047427450.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283406.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X7 XM_047427451.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283407.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X8 XM_047427452.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283408.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X9 XM_047427453.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283409.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X10 XM_047427454.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283410.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X11 XM_047427455.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283411.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X12 XM_047427456.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283412.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X13 XM_047427457.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283413.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X14 XM_047427458.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283414.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X15 XM_017018144.3:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_016873633.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X16 XM_047427459.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283415.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X17 XM_011520290.3:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_011518592.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X18 XM_047427460.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283416.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X19 XM_047427461.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283417.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X20 XM_047427462.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_047283418.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X21 XM_017018155.3:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_016873644.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X22 XM_017018154.2:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X1 XP_016873643.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X23 XM_047427463.1:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X2 XP_047283419.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X24 XM_047427464.1:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X2 XP_047283420.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X25 XM_017018157.2:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X2 XP_016873646.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X26 XM_047427465.1:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X2 XP_047283421.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X27 XM_047427466.1:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X2 XP_047283422.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X28 XM_011520297.3:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X2 XP_011518599.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X29 XM_047427467.1:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X2 XP_047283423.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X30 XM_047427468.1:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X2 XP_047283424.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X32 XM_047427469.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X3 XP_047283425.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X33 XM_047427470.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X4 XP_047283426.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X34 XM_047427471.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X4 XP_047283427.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X35 XM_047427472.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X4 XP_047283428.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X36 XM_047427473.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X4 XP_047283429.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X37 XM_047427474.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X4 XP_047283430.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X38 XM_047427475.1:c.998A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X4 XP_047283431.1:p.Glu333Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X39 XM_047427476.1:c.875A>G E [GAG] > G [GGG] Coding Sequence Variant
serine/threonine-protein kinase 33 isoform X5 XP_047283432.1:p.Glu292Gly E (Glu) > G (Gly) Missense Variant
STK33 transcript variant X31 XR_007062494.1:n.1392A>G N/A Non Coding Transcript Variant
STK33 transcript variant X40 XR_001747939.2:n.3482A>G 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.

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 T= C
GRCh38.p14 chr 11 NC_000011.10:g.8436089= NC_000011.10:g.8436089T>C
GRCh37.p13 chr 11 NC_000011.9:g.8457636= NC_000011.9:g.8457636T>C
STK33 transcript variant 1 NM_030906.4:c.998= NM_030906.4:c.998A>G
STK33 transcript variant 1 NM_030906.3:c.998= NM_030906.3:c.998A>G
STK33 transcript NM_030906.2:c.998= NM_030906.2:c.998A>G
STK33 transcript variant X21 XM_017018155.3:c.998= XM_017018155.3:c.998A>G
STK33 transcript variant X11 XM_017018155.2:c.998= XM_017018155.2:c.998A>G
STK33 transcript variant X19 XM_017018155.1:c.998= XM_017018155.1:c.998A>G
STK33 transcript variant X17 XM_011520290.3:c.998= XM_011520290.3:c.998A>G
STK33 transcript variant X7 XM_011520290.2:c.998= XM_011520290.2:c.998A>G
STK33 transcript variant X3 XM_011520290.1:c.998= XM_011520290.1:c.998A>G
STK33 transcript variant X15 XM_017018144.3:c.998= XM_017018144.3:c.998A>G
STK33 transcript variant X1 XM_017018144.2:c.998= XM_017018144.2:c.998A>G
STK33 transcript variant X2 XM_017018144.1:c.998= XM_017018144.1:c.998A>G
STK33 transcript variant X28 XM_011520297.3:c.875= XM_011520297.3:c.875A>G
STK33 transcript variant X14 XM_011520297.2:c.875= XM_011520297.2:c.875A>G
STK33 transcript variant X10 XM_011520297.1:c.875= XM_011520297.1:c.875A>G
STK33 transcript variant X40 XR_001747939.2:n.3482= XR_001747939.2:n.3482A>G
STK33 transcript variant X18 XR_001747939.1:n.3490= XR_001747939.1:n.3490A>G
STK33 transcript variant 16 NM_001352398.2:c.875= NM_001352398.2:c.875A>G
STK33 transcript variant 16 NM_001352398.1:c.875= NM_001352398.1:c.875A>G
STK33 transcript variant 15 NM_001352397.2:c.875= NM_001352397.2:c.875A>G
STK33 transcript variant 15 NM_001352397.1:c.875= NM_001352397.1:c.875A>G
STK33 transcript variant 14 NM_001352396.2:c.875= NM_001352396.2:c.875A>G
STK33 transcript variant 14 NM_001352396.1:c.875= NM_001352396.1:c.875A>G
STK33 transcript variant X3 XM_017018145.2:c.998= XM_017018145.2:c.998A>G
STK33 transcript variant X3 XM_017018145.1:c.998= XM_017018145.1:c.998A>G
STK33 transcript variant X1 XM_017018146.2:c.998= XM_017018146.2:c.998A>G
STK33 transcript variant X2 XM_017018146.1:c.998= XM_017018146.1:c.998A>G
STK33 transcript variant 7 NM_001352389.2:c.998= NM_001352389.2:c.998A>G
STK33 transcript variant 7 NM_001352389.1:c.998= NM_001352389.1:c.998A>G
STK33 transcript variant 6 NM_001352388.2:c.998= NM_001352388.2:c.998A>G
STK33 transcript variant 6 NM_001352388.1:c.998= NM_001352388.1:c.998A>G
STK33 transcript variant 9 NM_001352391.2:c.998= NM_001352391.2:c.998A>G
STK33 transcript variant 9 NM_001352391.1:c.998= NM_001352391.1:c.998A>G
STK33 transcript variant 8 NM_001352390.2:c.998= NM_001352390.2:c.998A>G
STK33 transcript variant 8 NM_001352390.1:c.998= NM_001352390.1:c.998A>G
STK33 transcript variant 10 NM_001352392.2:c.998= NM_001352392.2:c.998A>G
STK33 transcript variant 10 NM_001352392.1:c.998= NM_001352392.1:c.998A>G
STK33 transcript variant 4 NM_001289061.2:c.998= NM_001289061.2:c.998A>G
STK33 transcript variant 4 NM_001289061.1:c.998= NM_001289061.1:c.998A>G
STK33 transcript variant 5 NM_001352387.2:c.998= NM_001352387.2:c.998A>G
STK33 transcript variant 5 NM_001352387.1:c.998= NM_001352387.1:c.998A>G
STK33 transcript variant 11 NM_001352393.2:c.998= NM_001352393.2:c.998A>G
STK33 transcript variant 11 NM_001352393.1:c.998= NM_001352393.1:c.998A>G
STK33 transcript variant 12 NM_001352394.2:c.875= NM_001352394.2:c.875A>G
STK33 transcript variant 12 NM_001352394.1:c.875= NM_001352394.1:c.875A>G
STK33 transcript variant X22 XM_017018154.2:c.998= XM_017018154.2:c.998A>G
STK33 transcript variant X10 XM_017018154.1:c.998= XM_017018154.1:c.998A>G
STK33 transcript variant 13 NM_001352395.2:c.875= NM_001352395.2:c.875A>G
STK33 transcript variant 13 NM_001352395.1:c.875= NM_001352395.1:c.875A>G
STK33 transcript variant 17 NM_001352399.2:c.998= NM_001352399.2:c.998A>G
STK33 transcript variant 17 NM_001352399.1:c.998= NM_001352399.1:c.998A>G
STK33 transcript variant 2 NM_001289058.2:c.875= NM_001289058.2:c.875A>G
STK33 transcript variant 2 NM_001289058.1:c.875= NM_001289058.1:c.875A>G
STK33 transcript variant X25 XM_017018157.2:c.875= XM_017018157.2:c.875A>G
STK33 transcript variant X13 XM_017018157.1:c.875= XM_017018157.1:c.875A>G
STK33 transcript variant 3 NM_001289059.2:c.437= NM_001289059.2:c.437A>G
STK33 transcript variant 3 NM_001289059.1:c.437= NM_001289059.1:c.437A>G
STK33 transcript variant X32 XM_047427469.1:c.998= XM_047427469.1:c.998A>G
STK33 transcript variant X34 XM_047427471.1:c.998= XM_047427471.1:c.998A>G
STK33 transcript variant X19 XM_047427461.1:c.998= XM_047427461.1:c.998A>G
STK33 transcript variant X2 XM_047427447.1:c.998= XM_047427447.1:c.998A>G
STK33 transcript variant X6 XM_047427450.1:c.998= XM_047427450.1:c.998A>G
STK33 transcript variant X9 XM_047427453.1:c.998= XM_047427453.1:c.998A>G
STK33 transcript variant X11 XM_047427455.1:c.998= XM_047427455.1:c.998A>G
STK33 transcript variant X18 XM_047427460.1:c.998= XM_047427460.1:c.998A>G
STK33 transcript variant X8 XM_047427452.1:c.998= XM_047427452.1:c.998A>G
STK33 transcript variant X12 XM_047427456.1:c.998= XM_047427456.1:c.998A>G
STK33 transcript variant X10 XM_047427454.1:c.998= XM_047427454.1:c.998A>G
STK33 transcript variant X7 XM_047427451.1:c.998= XM_047427451.1:c.998A>G
STK33 transcript variant X4 XM_047427448.1:c.998= XM_047427448.1:c.998A>G
STK33 transcript variant X13 XM_047427457.1:c.998= XM_047427457.1:c.998A>G
STK33 transcript variant X5 XM_047427449.1:c.998= XM_047427449.1:c.998A>G
STK33 transcript variant X20 XM_047427462.1:c.998= XM_047427462.1:c.998A>G
STK33 transcript variant X33 XM_047427470.1:c.998= XM_047427470.1:c.998A>G
STK33 transcript variant X16 XM_047427459.1:c.998= XM_047427459.1:c.998A>G
STK33 transcript variant X14 XM_047427458.1:c.998= XM_047427458.1:c.998A>G
STK33 transcript variant X38 XM_047427475.1:c.998= XM_047427475.1:c.998A>G
STK33 transcript variant X24 XM_047427464.1:c.875= XM_047427464.1:c.875A>G
STK33 transcript variant X35 XM_047427472.1:c.998= XM_047427472.1:c.998A>G
STK33 transcript variant X29 XM_047427467.1:c.875= XM_047427467.1:c.875A>G
STK33 transcript variant X37 XM_047427474.1:c.998= XM_047427474.1:c.998A>G
STK33 transcript variant X30 XM_047427468.1:c.875= XM_047427468.1:c.875A>G
STK33 transcript variant X27 XM_047427466.1:c.875= XM_047427466.1:c.875A>G
STK33 transcript variant X26 XM_047427465.1:c.875= XM_047427465.1:c.875A>G
STK33 transcript variant X36 XM_047427473.1:c.998= XM_047427473.1:c.998A>G
STK33 transcript variant X31 XR_007062494.1:n.1392= XR_007062494.1:n.1392A>G
STK33 transcript variant X23 XM_047427463.1:c.875= XM_047427463.1:c.875A>G
STK33 transcript variant X39 XM_047427476.1:c.875= XM_047427476.1:c.875A>G
serine/threonine-protein kinase 33 isoform a NP_112168.1:p.Glu333= NP_112168.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_016873644.1:p.Glu333= XP_016873644.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_011518592.1:p.Glu333= XP_011518592.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_016873633.1:p.Glu333= XP_016873633.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X2 XP_011518599.1:p.Glu292= XP_011518599.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform d NP_001339327.1:p.Glu292= NP_001339327.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform d NP_001339326.1:p.Glu292= NP_001339326.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform d NP_001339325.1:p.Glu292= NP_001339325.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform X1 XP_016873634.1:p.Glu333= XP_016873634.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_016873635.1:p.Glu333= XP_016873635.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform a NP_001339318.1:p.Glu333= NP_001339318.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform a NP_001339317.1:p.Glu333= NP_001339317.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform a NP_001339320.1:p.Glu333= NP_001339320.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform a NP_001339319.1:p.Glu333= NP_001339319.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform a NP_001339321.1:p.Glu333= NP_001339321.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform a NP_001275990.1:p.Glu333= NP_001275990.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform a NP_001339316.1:p.Glu333= NP_001339316.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform a NP_001339322.1:p.Glu333= NP_001339322.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform b NP_001339323.1:p.Glu292= NP_001339323.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform X1 XP_016873643.1:p.Glu333= XP_016873643.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform b NP_001339324.1:p.Glu292= NP_001339324.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform e NP_001339328.1:p.Glu333= NP_001339328.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform b NP_001275987.1:p.Glu292= NP_001275987.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform X2 XP_016873646.1:p.Glu292= XP_016873646.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform c NP_001275988.1:p.Glu146= NP_001275988.1:p.Glu146Gly
serine/threonine-protein kinase 33 isoform X3 XP_047283425.1:p.Glu333= XP_047283425.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X4 XP_047283427.1:p.Glu333= XP_047283427.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283417.1:p.Glu333= XP_047283417.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283403.1:p.Glu333= XP_047283403.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283406.1:p.Glu333= XP_047283406.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283409.1:p.Glu333= XP_047283409.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283411.1:p.Glu333= XP_047283411.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283416.1:p.Glu333= XP_047283416.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283408.1:p.Glu333= XP_047283408.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283412.1:p.Glu333= XP_047283412.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283410.1:p.Glu333= XP_047283410.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283407.1:p.Glu333= XP_047283407.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283404.1:p.Glu333= XP_047283404.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283413.1:p.Glu333= XP_047283413.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283405.1:p.Glu333= XP_047283405.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283418.1:p.Glu333= XP_047283418.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X4 XP_047283426.1:p.Glu333= XP_047283426.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283415.1:p.Glu333= XP_047283415.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X1 XP_047283414.1:p.Glu333= XP_047283414.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X4 XP_047283431.1:p.Glu333= XP_047283431.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X2 XP_047283420.1:p.Glu292= XP_047283420.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform X4 XP_047283428.1:p.Glu333= XP_047283428.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X2 XP_047283423.1:p.Glu292= XP_047283423.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform X4 XP_047283430.1:p.Glu333= XP_047283430.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X2 XP_047283424.1:p.Glu292= XP_047283424.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform X2 XP_047283422.1:p.Glu292= XP_047283422.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform X2 XP_047283421.1:p.Glu292= XP_047283421.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform X4 XP_047283429.1:p.Glu333= XP_047283429.1:p.Glu333Gly
serine/threonine-protein kinase 33 isoform X2 XP_047283419.1:p.Glu292= XP_047283419.1:p.Glu292Gly
serine/threonine-protein kinase 33 isoform X5 XP_047283432.1:p.Glu292= XP_047283432.1:p.Glu292Gly
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, 3 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss4229709876 Apr 26, 2021 (155)
2 TOPMED ss4874537164 Apr 26, 2021 (155)
3 gnomAD - Genomes NC_000011.10 - 8436089 Apr 26, 2021 (155)
4 TopMed NC_000011.10 - 8436089 Apr 26, 2021 (155)
5 ALFA NC_000011.10 - 8436089 Apr 26, 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
370810986, 90082820, 13186941423, ss4229709876, ss4874537164 NC_000011.10:8436088:T:C NC_000011.10:8436088:T:C (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1455266125

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.post820+afb47a3d