Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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.

rs1489569724

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:52495501 (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>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.00000 (0/14050, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TUT4 : 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 A=1.00000 T=0.00000 1.0 0.0 0.0 N/A
European Sub 9690 A=1.0000 T=0.0000 1.0 0.0 0.0 N/A
African Sub 2898 A=1.0000 T=0.0000 1.0 0.0 0.0 N/A
African Others Sub 114 A=1.000 T=0.000 1.0 0.0 0.0 N/A
African American Sub 2784 A=1.0000 T=0.0000 1.0 0.0 0.0 N/A
Asian Sub 112 A=1.000 T=0.000 1.0 0.0 0.0 N/A
East Asian Sub 86 A=1.00 T=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 26 A=1.00 T=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 A=1.000 T=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 A=1.000 T=0.000 1.0 0.0 0.0 N/A
South Asian Sub 98 A=1.00 T=0.00 1.0 0.0 0.0 N/A
Other Sub 496 A=1.000 T=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
Allele Frequency Aggregator Total Global 14050 A=1.00000 T=0.00000
Allele Frequency Aggregator European Sub 9690 A=1.0000 T=0.0000
Allele Frequency Aggregator African Sub 2898 A=1.0000 T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 A=1.000 T=0.000
Allele Frequency Aggregator Other Sub 496 A=1.000 T=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 A=1.000 T=0.000
Allele Frequency Aggregator Asian Sub 112 A=1.000 T=0.000
Allele Frequency Aggregator South Asian Sub 98 A=1.00 T=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 1 NC_000001.11:g.52495501A>T
GRCh37.p13 chr 1 NC_000001.10:g.52961173A>T
Gene: TUT4, terminal uridylyl transferase 4 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
TUT4 transcript variant 2 NM_015269.2:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform b NP_056084.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant 1 NM_001009881.3:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform a NP_001009881.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X49 XM_047416428.1:c. N/A Genic Upstream Transcript Variant
TUT4 transcript variant X1 XM_005270676.3:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X1 XP_005270733.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X2 XM_011541097.2:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X1 XP_011539399.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X3 XM_005270678.3:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X2 XP_005270735.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X4 XM_005270679.3:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X3 XP_005270736.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X5 XM_047416324.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X3 XP_047272280.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X6 XM_047416325.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X4 XP_047272281.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X7 XM_047416326.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X5 XP_047272282.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X8 XM_005270680.4:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X6 XP_005270737.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X9 XM_047416327.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X6 XP_047272283.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X10 XM_047416329.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X7 XP_047272285.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X11 XM_047416330.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X8 XP_047272286.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X12 XM_017000803.2:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X9 XP_016856292.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X13 XM_047416332.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X10 XP_047272288.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X14 XM_047416334.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X11 XP_047272290.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X15 XM_047416339.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X12 XP_047272295.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X16 XM_047416340.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X13 XP_047272296.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X17 XM_005270681.3:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X14 XP_005270738.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X18 XM_047416347.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X15 XP_047272303.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X19 XM_017000804.3:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X16 XP_016856293.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X20 XM_047416349.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X17 XP_047272305.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X21 XM_047416350.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X18 XP_047272306.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X22 XM_047416351.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X19 XP_047272307.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X23 XM_017000805.3:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X20 XP_016856294.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X24 XM_047416355.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X21 XP_047272311.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X25 XM_047416364.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X22 XP_047272320.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X26 XM_047416369.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X23 XP_047272325.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X27 XM_047416371.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X24 XP_047272327.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X28 XM_017000806.2:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X25 XP_016856295.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X29 XM_047416380.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X26 XP_047272336.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X30 XM_047416381.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X27 XP_047272337.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X31 XM_017000807.3:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X28 XP_016856296.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X32 XM_011541099.2:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X29 XP_011539401.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X33 XM_047416388.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X30 XP_047272344.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X34 XM_047416389.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X31 XP_047272345.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X35 XM_047416392.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X32 XP_047272348.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X36 XM_005270682.3:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X33 XP_005270739.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X37 XM_047416394.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X34 XP_047272350.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X38 XM_047416398.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X35 XP_047272354.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X39 XM_017000808.2:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X36 XP_016856297.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X40 XM_047416406.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X37 XP_047272362.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X41 XM_047416409.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X38 XP_047272365.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X42 XM_047416411.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X39 XP_047272367.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X43 XM_017000810.3:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X40 XP_016856299.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X44 XM_047416413.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X41 XP_047272369.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X45 XM_047416416.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X42 XP_047272372.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X46 XM_047416417.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X43 XP_047272373.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X47 XM_047416421.1:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X44 XP_047272377.1:p.Leu398Met L (Leu) > M (Met) Missense Variant
TUT4 transcript variant X48 XM_017000818.2:c.1192T>A L [TTG] > M [ATG] Coding Sequence Variant
terminal uridylyltransferase 4 isoform X45 XP_016856307.1:p.Leu398Met L (Leu) > M (Met) Missense 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= T
GRCh38.p14 chr 1 NC_000001.11:g.52495501= NC_000001.11:g.52495501A>T
GRCh37.p13 chr 1 NC_000001.10:g.52961173= NC_000001.10:g.52961173A>T
TUT4 transcript variant X8 XM_005270680.4:c.1192= XM_005270680.4:c.1192T>A
TUT4 transcript variant X7 XM_005270680.3:c.1192= XM_005270680.3:c.1192T>A
ZCCHC11 transcript variant X7 XM_005270680.2:c.1192= XM_005270680.2:c.1192T>A
ZCCHC11 transcript variant X5 XM_005270680.1:c.1192= XM_005270680.1:c.1192T>A
TUT4 transcript variant 1 NM_001009881.3:c.1192= NM_001009881.3:c.1192T>A
TUT4 transcript variant 1 NM_001009881.2:c.1192= NM_001009881.2:c.1192T>A
TUT4 transcript variant X3 XM_005270678.3:c.1192= XM_005270678.3:c.1192T>A
TUT4 transcript variant X5 XM_005270678.2:c.1192= XM_005270678.2:c.1192T>A
ZCCHC11 transcript variant X3 XM_005270678.1:c.1192= XM_005270678.1:c.1192T>A
TUT4 transcript variant X19 XM_017000804.3:c.1192= XM_017000804.3:c.1192T>A
TUT4 transcript variant X11 XM_017000804.2:c.1192= XM_017000804.2:c.1192T>A
ZCCHC11 transcript variant X11 XM_017000804.1:c.1192= XM_017000804.1:c.1192T>A
TUT4 transcript variant X1 XM_005270676.3:c.1192= XM_005270676.3:c.1192T>A
TUT4 transcript variant X1 XM_005270676.2:c.1192= XM_005270676.2:c.1192T>A
ZCCHC11 transcript variant X1 XM_005270676.1:c.1192= XM_005270676.1:c.1192T>A
TUT4 transcript variant X4 XM_005270679.3:c.1192= XM_005270679.3:c.1192T>A
TUT4 transcript variant X6 XM_005270679.2:c.1192= XM_005270679.2:c.1192T>A
ZCCHC11 transcript variant X4 XM_005270679.1:c.1192= XM_005270679.1:c.1192T>A
TUT4 transcript variant X23 XM_017000805.3:c.1192= XM_017000805.3:c.1192T>A
TUT4 transcript variant X12 XM_017000805.2:c.1192= XM_017000805.2:c.1192T>A
ZCCHC11 transcript variant X12 XM_017000805.1:c.1192= XM_017000805.1:c.1192T>A
TUT4 transcript variant X17 XM_005270681.3:c.1192= XM_005270681.3:c.1192T>A
TUT4 transcript variant X10 XM_005270681.2:c.1192= XM_005270681.2:c.1192T>A
ZCCHC11 transcript variant X6 XM_005270681.1:c.1192= XM_005270681.1:c.1192T>A
TUT4 transcript variant X31 XM_017000807.3:c.1192= XM_017000807.3:c.1192T>A
TUT4 transcript variant X15 XM_017000807.2:c.1192= XM_017000807.2:c.1192T>A
ZCCHC11 transcript variant X15 XM_017000807.1:c.1192= XM_017000807.1:c.1192T>A
TUT4 transcript variant X43 XM_017000810.3:c.1192= XM_017000810.3:c.1192T>A
TUT4 transcript variant X21 XM_017000810.2:c.1192= XM_017000810.2:c.1192T>A
ZCCHC11 transcript variant X21 XM_017000810.1:c.1192= XM_017000810.1:c.1192T>A
TUT4 transcript variant X36 XM_005270682.3:c.1192= XM_005270682.3:c.1192T>A
TUT4 transcript variant X17 XM_005270682.2:c.1192= XM_005270682.2:c.1192T>A
ZCCHC11 transcript variant X7 XM_005270682.1:c.1192= XM_005270682.1:c.1192T>A
TUT4 transcript variant 2 NM_015269.2:c.1192= NM_015269.2:c.1192T>A
TUT4 transcript variant X2 XM_011541097.2:c.1192= XM_011541097.2:c.1192T>A
TUT4 transcript variant X2 XM_011541097.1:c.1192= XM_011541097.1:c.1192T>A
TUT4 transcript variant X12 XM_017000803.2:c.1192= XM_017000803.2:c.1192T>A
TUT4 transcript variant X9 XM_017000803.1:c.1192= XM_017000803.1:c.1192T>A
TUT4 transcript variant X28 XM_017000806.2:c.1192= XM_017000806.2:c.1192T>A
TUT4 transcript variant X14 XM_017000806.1:c.1192= XM_017000806.1:c.1192T>A
TUT4 transcript variant X32 XM_011541099.2:c.1192= XM_011541099.2:c.1192T>A
TUT4 transcript variant X16 XM_011541099.1:c.1192= XM_011541099.1:c.1192T>A
TUT4 transcript variant X39 XM_017000808.2:c.1192= XM_017000808.2:c.1192T>A
TUT4 transcript variant X18 XM_017000808.1:c.1192= XM_017000808.1:c.1192T>A
TUT4 transcript variant X48 XM_017000818.2:c.1192= XM_017000818.2:c.1192T>A
TUT4 transcript variant X34 XM_017000818.1:c.1192= XM_017000818.1:c.1192T>A
TUT4 transcript variant X6 XM_047416325.1:c.1192= XM_047416325.1:c.1192T>A
TUT4 transcript variant X7 XM_047416326.1:c.1192= XM_047416326.1:c.1192T>A
TUT4 transcript variant X9 XM_047416327.1:c.1192= XM_047416327.1:c.1192T>A
ZCCHC11 transcript variant 3 NM_001009882.1:c.1192= NM_001009882.1:c.1192T>A
TUT4 transcript variant X5 XM_047416324.1:c.1192= XM_047416324.1:c.1192T>A
TUT4 transcript variant X13 XM_047416332.1:c.1192= XM_047416332.1:c.1192T>A
TUT4 transcript variant X15 XM_047416339.1:c.1192= XM_047416339.1:c.1192T>A
TUT4 transcript variant X16 XM_047416340.1:c.1192= XM_047416340.1:c.1192T>A
TUT4 transcript variant X20 XM_047416349.1:c.1192= XM_047416349.1:c.1192T>A
TUT4 transcript variant X22 XM_047416351.1:c.1192= XM_047416351.1:c.1192T>A
TUT4 transcript variant X10 XM_047416329.1:c.1192= XM_047416329.1:c.1192T>A
TUT4 transcript variant X11 XM_047416330.1:c.1192= XM_047416330.1:c.1192T>A
TUT4 transcript variant X14 XM_047416334.1:c.1192= XM_047416334.1:c.1192T>A
TUT4 transcript variant X25 XM_047416364.1:c.1192= XM_047416364.1:c.1192T>A
TUT4 transcript variant X27 XM_047416371.1:c.1192= XM_047416371.1:c.1192T>A
TUT4 transcript variant X18 XM_047416347.1:c.1192= XM_047416347.1:c.1192T>A
TUT4 transcript variant X29 XM_047416380.1:c.1192= XM_047416380.1:c.1192T>A
TUT4 transcript variant X30 XM_047416381.1:c.1192= XM_047416381.1:c.1192T>A
TUT4 transcript variant X21 XM_047416350.1:c.1192= XM_047416350.1:c.1192T>A
TUT4 transcript variant X24 XM_047416355.1:c.1192= XM_047416355.1:c.1192T>A
TUT4 transcript variant X26 XM_047416369.1:c.1192= XM_047416369.1:c.1192T>A
TUT4 transcript variant X37 XM_047416394.1:c.1192= XM_047416394.1:c.1192T>A
TUT4 transcript variant X38 XM_047416398.1:c.1192= XM_047416398.1:c.1192T>A
TUT4 transcript variant X40 XM_047416406.1:c.1192= XM_047416406.1:c.1192T>A
TUT4 transcript variant X41 XM_047416409.1:c.1192= XM_047416409.1:c.1192T>A
TUT4 transcript variant X42 XM_047416411.1:c.1192= XM_047416411.1:c.1192T>A
TUT4 transcript variant X33 XM_047416388.1:c.1192= XM_047416388.1:c.1192T>A
TUT4 transcript variant X34 XM_047416389.1:c.1192= XM_047416389.1:c.1192T>A
TUT4 transcript variant X35 XM_047416392.1:c.1192= XM_047416392.1:c.1192T>A
TUT4 transcript variant X45 XM_047416416.1:c.1192= XM_047416416.1:c.1192T>A
TUT4 transcript variant X46 XM_047416417.1:c.1192= XM_047416417.1:c.1192T>A
TUT4 transcript variant X47 XM_047416421.1:c.1192= XM_047416421.1:c.1192T>A
TUT4 transcript variant X44 XM_047416413.1:c.1192= XM_047416413.1:c.1192T>A
terminal uridylyltransferase 4 isoform X6 XP_005270737.1:p.Leu398= XP_005270737.1:p.Leu398Met
terminal uridylyltransferase 4 isoform a NP_001009881.1:p.Leu398= NP_001009881.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X2 XP_005270735.1:p.Leu398= XP_005270735.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X16 XP_016856293.1:p.Leu398= XP_016856293.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X1 XP_005270733.1:p.Leu398= XP_005270733.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X3 XP_005270736.1:p.Leu398= XP_005270736.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X20 XP_016856294.1:p.Leu398= XP_016856294.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X14 XP_005270738.1:p.Leu398= XP_005270738.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X28 XP_016856296.1:p.Leu398= XP_016856296.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X40 XP_016856299.1:p.Leu398= XP_016856299.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X33 XP_005270739.1:p.Leu398= XP_005270739.1:p.Leu398Met
terminal uridylyltransferase 4 isoform b NP_056084.1:p.Leu398= NP_056084.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X1 XP_011539399.1:p.Leu398= XP_011539399.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X9 XP_016856292.1:p.Leu398= XP_016856292.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X25 XP_016856295.1:p.Leu398= XP_016856295.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X29 XP_011539401.1:p.Leu398= XP_011539401.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X36 XP_016856297.1:p.Leu398= XP_016856297.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X45 XP_016856307.1:p.Leu398= XP_016856307.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X4 XP_047272281.1:p.Leu398= XP_047272281.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X5 XP_047272282.1:p.Leu398= XP_047272282.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X6 XP_047272283.1:p.Leu398= XP_047272283.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X3 XP_047272280.1:p.Leu398= XP_047272280.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X10 XP_047272288.1:p.Leu398= XP_047272288.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X12 XP_047272295.1:p.Leu398= XP_047272295.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X13 XP_047272296.1:p.Leu398= XP_047272296.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X17 XP_047272305.1:p.Leu398= XP_047272305.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X19 XP_047272307.1:p.Leu398= XP_047272307.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X7 XP_047272285.1:p.Leu398= XP_047272285.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X8 XP_047272286.1:p.Leu398= XP_047272286.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X11 XP_047272290.1:p.Leu398= XP_047272290.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X22 XP_047272320.1:p.Leu398= XP_047272320.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X24 XP_047272327.1:p.Leu398= XP_047272327.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X15 XP_047272303.1:p.Leu398= XP_047272303.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X26 XP_047272336.1:p.Leu398= XP_047272336.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X27 XP_047272337.1:p.Leu398= XP_047272337.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X18 XP_047272306.1:p.Leu398= XP_047272306.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X21 XP_047272311.1:p.Leu398= XP_047272311.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X23 XP_047272325.1:p.Leu398= XP_047272325.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X34 XP_047272350.1:p.Leu398= XP_047272350.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X35 XP_047272354.1:p.Leu398= XP_047272354.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X37 XP_047272362.1:p.Leu398= XP_047272362.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X38 XP_047272365.1:p.Leu398= XP_047272365.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X39 XP_047272367.1:p.Leu398= XP_047272367.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X30 XP_047272344.1:p.Leu398= XP_047272344.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X31 XP_047272345.1:p.Leu398= XP_047272345.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X32 XP_047272348.1:p.Leu398= XP_047272348.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X42 XP_047272372.1:p.Leu398= XP_047272372.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X43 XP_047272373.1:p.Leu398= XP_047272373.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X44 XP_047272377.1:p.Leu398= XP_047272377.1:p.Leu398Met
terminal uridylyltransferase 4 isoform X41 XP_047272369.1:p.Leu398= XP_047272369.1:p.Leu398Met
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 Frequency submission
No Submitter Submission ID Date (Build)
1 ALFA NC_000001.11 - 52495501 Apr 25, 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
313659427 NC_000001.11:52495500:A:T NC_000001.11:52495500:A:T (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 rs1489569724

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