Name: rs1481912801
Published: September 21, 2022
License: Open Access

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.

rs1481912801

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:52431228 (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>G
Variation Type: SNV Single Nucleotide Variation
Frequency: None

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TUT4 : Missense Variant
Publications: 0 citations
Genomic View: See rs on genome

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

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.52431228A>G
GRCh37.p13 chr 1	NC_000001.10:g.52896900A>G

Gene: TUT4, terminal uridylyl transferase 4 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TUT4 transcript variant 2	NM_015269.2:c.4493T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform b	NP_056084.1:p.Leu1498Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant 1	NM_001009881.3:c.4496T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform a	NP_001009881.1:p.Leu1499P… NP_001009881.1:p.Leu1499Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X48	XM_017000818.2:c.	N/A	Genic Downstream Transcript Variant
TUT4 transcript variant X1	XM_005270676.3:c.4496T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X1	XP_005270733.1:p.Leu1499P… XP_005270733.1:p.Leu1499Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X2	XM_011541097.2:c.4496T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X1	XP_011539399.1:p.Leu1499P… XP_011539399.1:p.Leu1499Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X3	XM_005270678.3:c.4493T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X2	XP_005270735.1:p.Leu1498P… XP_005270735.1:p.Leu1498Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X4	XM_005270679.3:c.4481T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X3	XP_005270736.1:p.Leu1494P… XP_005270736.1:p.Leu1494Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X5	XM_047416324.1:c.4481T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X3	XP_047272280.1:p.Leu1494P… XP_047272280.1:p.Leu1494Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X6	XM_047416325.1:c.4496T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X4	XP_047272281.1:p.Leu1499P… XP_047272281.1:p.Leu1499Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X7	XM_047416326.1:c.4493T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X5	XP_047272282.1:p.Leu1498P… XP_047272282.1:p.Leu1498Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X8	XM_005270680.4:c.4481T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X6	XP_005270737.1:p.Leu1494P… XP_005270737.1:p.Leu1494Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X9	XM_047416327.1:c.4481T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X6	XP_047272283.1:p.Leu1494P… XP_047272283.1:p.Leu1494Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X10	XM_047416329.1:c.4412T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X7	XP_047272285.1:p.Leu1471P… XP_047272285.1:p.Leu1471Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X11	XM_047416330.1:c.4409T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X8	XP_047272286.1:p.Leu1470P… XP_047272286.1:p.Leu1470Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X12	XM_017000803.2:c.4400T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X9	XP_016856292.1:p.Leu1467P… XP_016856292.1:p.Leu1467Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X13	XM_047416332.1:c.4415T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X10	XP_047272288.1:p.Leu1472P… XP_047272288.1:p.Leu1472Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X14	XM_047416334.1:c.4394T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X11	XP_047272290.1:p.Leu1465P… XP_047272290.1:p.Leu1465Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X15	XM_047416339.1:c.4409T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X12	XP_047272295.1:p.Leu1470P… XP_047272295.1:p.Leu1470Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X16	XM_047416340.1:c.4406T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X13	XP_047272296.1:p.Leu1469P… XP_047272296.1:p.Leu1469Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X17	XM_005270681.3:c.4382T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X14	XP_005270738.1:p.Leu1461P… XP_005270738.1:p.Leu1461Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X18	XM_047416347.1:c.4379T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X15	XP_047272303.1:p.Leu1460P… XP_047272303.1:p.Leu1460Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X19	XM_017000804.3:c.4400T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X16	XP_016856293.1:p.Leu1467P… XP_016856293.1:p.Leu1467Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X20	XM_047416349.1:c.4394T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X17	XP_047272305.1:p.Leu1465P… XP_047272305.1:p.Leu1465Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X21	XM_047416350.1:c.4367T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X18	XP_047272306.1:p.Leu1456P… XP_047272306.1:p.Leu1456Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X22	XM_047416351.1:c.4379T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X19	XP_047272307.1:p.Leu1460P… XP_047272307.1:p.Leu1460Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X23	XM_017000805.3:c.4367T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X20	XP_016856294.1:p.Leu1456P… XP_016856294.1:p.Leu1456Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X24	XM_047416355.1:c.4301T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X21	XP_047272311.1:p.Leu1434P… XP_047272311.1:p.Leu1434Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X25	XM_047416364.1:c.4301T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X22	XP_047272320.1:p.Leu1434P… XP_047272320.1:p.Leu1434Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X26	XM_047416369.1:c.4280T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X23	XP_047272325.1:p.Leu1427P… XP_047272325.1:p.Leu1427Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X27	XM_047416371.1:c.4298T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X24	XP_047272327.1:p.Leu1433P… XP_047272327.1:p.Leu1433Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X28	XM_017000806.2:c.4268T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X25	XP_016856295.1:p.Leu1423P… XP_016856295.1:p.Leu1423Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X29	XM_047416380.1:c.4286T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X26	XP_047272336.1:p.Leu1429P… XP_047272336.1:p.Leu1429Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X30	XM_047416381.1:c.4280T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X27	XP_047272337.1:p.Leu1427P… XP_047272337.1:p.Leu1427Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X31	XM_017000807.3:c.4268T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X28	XP_016856296.1:p.Leu1423P… XP_016856296.1:p.Leu1423Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X32	XM_011541099.2:c.4202T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X29	XP_011539401.1:p.Leu1401P… XP_011539401.1:p.Leu1401Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X33	XM_047416388.1:c.4196T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X30	XP_047272344.1:p.Leu1399P… XP_047272344.1:p.Leu1399Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X34	XM_047416389.1:c.4187T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X31	XP_047272345.1:p.Leu1396P… XP_047272345.1:p.Leu1396Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X35	XM_047416392.1:c.4169T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X32	XP_047272348.1:p.Leu1390P… XP_047272348.1:p.Leu1390Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X36	XM_005270682.3:c.4163T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X33	XP_005270739.1:p.Leu1388P… XP_005270739.1:p.Leu1388Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X37	XM_047416394.1:c.4181T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X34	XP_047272350.1:p.Leu1394P… XP_047272350.1:p.Leu1394Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X38	XM_047416398.1:c.4169T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X35	XP_047272354.1:p.Leu1390P… XP_047272354.1:p.Leu1390Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X39	XM_017000808.2:c.4148T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X36	XP_016856297.1:p.Leu1383P… XP_016856297.1:p.Leu1383Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X40	XM_047416406.1:c.4166T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X37	XP_047272362.1:p.Leu1389P… XP_047272362.1:p.Leu1389Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X41	XM_047416409.1:c.4160T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X38	XP_047272365.1:p.Leu1387P… XP_047272365.1:p.Leu1387Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X42	XM_047416411.1:c.4154T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X39	XP_047272367.1:p.Leu1385P… XP_047272367.1:p.Leu1385Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X43	XM_017000810.3:c.4148T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X40	XP_016856299.1:p.Leu1383P… XP_016856299.1:p.Leu1383Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X44	XM_047416413.1:c.4088T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X41	XP_047272369.1:p.Leu1363P… XP_047272369.1:p.Leu1363Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X45	XM_047416416.1:c.4073T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X42	XP_047272372.1:p.Leu1358P… XP_047272372.1:p.Leu1358Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X46	XM_047416417.1:c.4049T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X43	XP_047272373.1:p.Leu1350P… XP_047272373.1:p.Leu1350Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X47	XM_047416421.1:c.4034T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X44	XP_047272377.1:p.Leu1345P… XP_047272377.1:p.Leu1345Pro	L (Leu) > P (Pro)	Missense Variant
TUT4 transcript variant X49	XM_047416428.1:c.2276T>C	L [CTC] > P [CCC]	Coding Sequence Variant
terminal uridylyltransferase 4 isoform X46	XP_047272384.1:p.Leu759Pro	L (Leu) > P (Pro)	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

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=	G
GRCh38.p14 chr 1	NC_000001.11:g.52431228=	NC_000001.11:g.52431228A>G
GRCh37.p13 chr 1	NC_000001.10:g.52896900=	NC_000001.10:g.52896900A>G
TUT4 transcript variant X8	XM_005270680.4:c.4481=	XM_005270680.4:c.4481T>C
TUT4 transcript variant X7	XM_005270680.3:c.4481=	XM_005270680.3:c.4481T>C
ZCCHC11 transcript variant X7	XM_005270680.2:c.4481=	XM_005270680.2:c.4481T>C
ZCCHC11 transcript variant X5	XM_005270680.1:c.4481=	XM_005270680.1:c.4481T>C
TUT4 transcript variant 1	NM_001009881.3:c.4496=	NM_001009881.3:c.4496T>C
TUT4 transcript variant 1	NM_001009881.2:c.4496=	NM_001009881.2:c.4496T>C
TUT4 transcript variant X3	XM_005270678.3:c.4493=	XM_005270678.3:c.4493T>C
TUT4 transcript variant X5	XM_005270678.2:c.4493=	XM_005270678.2:c.4493T>C
ZCCHC11 transcript variant X3	XM_005270678.1:c.4493=	XM_005270678.1:c.4493T>C
TUT4 transcript variant X19	XM_017000804.3:c.4400=	XM_017000804.3:c.4400T>C
TUT4 transcript variant X11	XM_017000804.2:c.4400=	XM_017000804.2:c.4400T>C
ZCCHC11 transcript variant X11	XM_017000804.1:c.4400=	XM_017000804.1:c.4400T>C
TUT4 transcript variant X1	XM_005270676.3:c.4496=	XM_005270676.3:c.4496T>C
TUT4 transcript variant X1	XM_005270676.2:c.4496=	XM_005270676.2:c.4496T>C
ZCCHC11 transcript variant X1	XM_005270676.1:c.4496=	XM_005270676.1:c.4496T>C
TUT4 transcript variant X4	XM_005270679.3:c.4481=	XM_005270679.3:c.4481T>C
TUT4 transcript variant X6	XM_005270679.2:c.4481=	XM_005270679.2:c.4481T>C
ZCCHC11 transcript variant X4	XM_005270679.1:c.4481=	XM_005270679.1:c.4481T>C
TUT4 transcript variant X23	XM_017000805.3:c.4367=	XM_017000805.3:c.4367T>C
TUT4 transcript variant X12	XM_017000805.2:c.4367=	XM_017000805.2:c.4367T>C
ZCCHC11 transcript variant X12	XM_017000805.1:c.4367=	XM_017000805.1:c.4367T>C
TUT4 transcript variant X17	XM_005270681.3:c.4382=	XM_005270681.3:c.4382T>C
TUT4 transcript variant X10	XM_005270681.2:c.4382=	XM_005270681.2:c.4382T>C
ZCCHC11 transcript variant X6	XM_005270681.1:c.4382=	XM_005270681.1:c.4382T>C
TUT4 transcript variant X31	XM_017000807.3:c.4268=	XM_017000807.3:c.4268T>C
TUT4 transcript variant X15	XM_017000807.2:c.4268=	XM_017000807.2:c.4268T>C
ZCCHC11 transcript variant X15	XM_017000807.1:c.4268=	XM_017000807.1:c.4268T>C
TUT4 transcript variant X43	XM_017000810.3:c.4148=	XM_017000810.3:c.4148T>C
TUT4 transcript variant X21	XM_017000810.2:c.4148=	XM_017000810.2:c.4148T>C
ZCCHC11 transcript variant X21	XM_017000810.1:c.4148=	XM_017000810.1:c.4148T>C
TUT4 transcript variant X36	XM_005270682.3:c.4163=	XM_005270682.3:c.4163T>C
TUT4 transcript variant X17	XM_005270682.2:c.4163=	XM_005270682.2:c.4163T>C
ZCCHC11 transcript variant X7	XM_005270682.1:c.4163=	XM_005270682.1:c.4163T>C
TUT4 transcript variant 2	NM_015269.2:c.4493=	NM_015269.2:c.4493T>C
TUT4 transcript variant X2	XM_011541097.2:c.4496=	XM_011541097.2:c.4496T>C
TUT4 transcript variant X2	XM_011541097.1:c.4496=	XM_011541097.1:c.4496T>C
TUT4 transcript variant X12	XM_017000803.2:c.4400=	XM_017000803.2:c.4400T>C
TUT4 transcript variant X9	XM_017000803.1:c.4400=	XM_017000803.1:c.4400T>C
TUT4 transcript variant X28	XM_017000806.2:c.4268=	XM_017000806.2:c.4268T>C
TUT4 transcript variant X14	XM_017000806.1:c.4268=	XM_017000806.1:c.4268T>C
TUT4 transcript variant X32	XM_011541099.2:c.4202=	XM_011541099.2:c.4202T>C
TUT4 transcript variant X16	XM_011541099.1:c.4202=	XM_011541099.1:c.4202T>C
TUT4 transcript variant X39	XM_017000808.2:c.4148=	XM_017000808.2:c.4148T>C
TUT4 transcript variant X18	XM_017000808.1:c.4148=	XM_017000808.1:c.4148T>C
TUT4 transcript variant X6	XM_047416325.1:c.4496=	XM_047416325.1:c.4496T>C
TUT4 transcript variant X7	XM_047416326.1:c.4493=	XM_047416326.1:c.4493T>C
TUT4 transcript variant X9	XM_047416327.1:c.4481=	XM_047416327.1:c.4481T>C
ZCCHC11 transcript variant 3	NM_001009882.1:c.4481=	NM_001009882.1:c.4481T>C
TUT4 transcript variant X5	XM_047416324.1:c.4481=	XM_047416324.1:c.4481T>C
TUT4 transcript variant X13	XM_047416332.1:c.4415=	XM_047416332.1:c.4415T>C
TUT4 transcript variant X15	XM_047416339.1:c.4409=	XM_047416339.1:c.4409T>C
TUT4 transcript variant X16	XM_047416340.1:c.4406=	XM_047416340.1:c.4406T>C
TUT4 transcript variant X20	XM_047416349.1:c.4394=	XM_047416349.1:c.4394T>C
TUT4 transcript variant X22	XM_047416351.1:c.4379=	XM_047416351.1:c.4379T>C
TUT4 transcript variant X10	XM_047416329.1:c.4412=	XM_047416329.1:c.4412T>C
TUT4 transcript variant X11	XM_047416330.1:c.4409=	XM_047416330.1:c.4409T>C
TUT4 transcript variant X14	XM_047416334.1:c.4394=	XM_047416334.1:c.4394T>C
TUT4 transcript variant X25	XM_047416364.1:c.4301=	XM_047416364.1:c.4301T>C
TUT4 transcript variant X27	XM_047416371.1:c.4298=	XM_047416371.1:c.4298T>C
TUT4 transcript variant X18	XM_047416347.1:c.4379=	XM_047416347.1:c.4379T>C
TUT4 transcript variant X29	XM_047416380.1:c.4286=	XM_047416380.1:c.4286T>C
TUT4 transcript variant X30	XM_047416381.1:c.4280=	XM_047416381.1:c.4280T>C
TUT4 transcript variant X21	XM_047416350.1:c.4367=	XM_047416350.1:c.4367T>C
TUT4 transcript variant X24	XM_047416355.1:c.4301=	XM_047416355.1:c.4301T>C
TUT4 transcript variant X26	XM_047416369.1:c.4280=	XM_047416369.1:c.4280T>C
TUT4 transcript variant X37	XM_047416394.1:c.4181=	XM_047416394.1:c.4181T>C
TUT4 transcript variant X38	XM_047416398.1:c.4169=	XM_047416398.1:c.4169T>C
TUT4 transcript variant X40	XM_047416406.1:c.4166=	XM_047416406.1:c.4166T>C
TUT4 transcript variant X41	XM_047416409.1:c.4160=	XM_047416409.1:c.4160T>C
TUT4 transcript variant X42	XM_047416411.1:c.4154=	XM_047416411.1:c.4154T>C
TUT4 transcript variant X33	XM_047416388.1:c.4196=	XM_047416388.1:c.4196T>C
TUT4 transcript variant X34	XM_047416389.1:c.4187=	XM_047416389.1:c.4187T>C
TUT4 transcript variant X35	XM_047416392.1:c.4169=	XM_047416392.1:c.4169T>C
TUT4 transcript variant X45	XM_047416416.1:c.4073=	XM_047416416.1:c.4073T>C
TUT4 transcript variant X46	XM_047416417.1:c.4049=	XM_047416417.1:c.4049T>C
TUT4 transcript variant X47	XM_047416421.1:c.4034=	XM_047416421.1:c.4034T>C
TUT4 transcript variant X44	XM_047416413.1:c.4088=	XM_047416413.1:c.4088T>C
TUT4 transcript variant X49	XM_047416428.1:c.2276=	XM_047416428.1:c.2276T>C
terminal uridylyltransferase 4 isoform X6	XP_005270737.1:p.Leu1494=	XP_005270737.1:p.Leu1494Pro
terminal uridylyltransferase 4 isoform a	NP_001009881.1:p.Leu1499=	NP_001009881.1:p.Leu1499Pro
terminal uridylyltransferase 4 isoform X2	XP_005270735.1:p.Leu1498=	XP_005270735.1:p.Leu1498Pro
terminal uridylyltransferase 4 isoform X16	XP_016856293.1:p.Leu1467=	XP_016856293.1:p.Leu1467Pro
terminal uridylyltransferase 4 isoform X1	XP_005270733.1:p.Leu1499=	XP_005270733.1:p.Leu1499Pro
terminal uridylyltransferase 4 isoform X3	XP_005270736.1:p.Leu1494=	XP_005270736.1:p.Leu1494Pro
terminal uridylyltransferase 4 isoform X20	XP_016856294.1:p.Leu1456=	XP_016856294.1:p.Leu1456Pro
terminal uridylyltransferase 4 isoform X14	XP_005270738.1:p.Leu1461=	XP_005270738.1:p.Leu1461Pro
terminal uridylyltransferase 4 isoform X28	XP_016856296.1:p.Leu1423=	XP_016856296.1:p.Leu1423Pro
terminal uridylyltransferase 4 isoform X40	XP_016856299.1:p.Leu1383=	XP_016856299.1:p.Leu1383Pro
terminal uridylyltransferase 4 isoform X33	XP_005270739.1:p.Leu1388=	XP_005270739.1:p.Leu1388Pro
terminal uridylyltransferase 4 isoform b	NP_056084.1:p.Leu1498=	NP_056084.1:p.Leu1498Pro
terminal uridylyltransferase 4 isoform X1	XP_011539399.1:p.Leu1499=	XP_011539399.1:p.Leu1499Pro
terminal uridylyltransferase 4 isoform X9	XP_016856292.1:p.Leu1467=	XP_016856292.1:p.Leu1467Pro
terminal uridylyltransferase 4 isoform X25	XP_016856295.1:p.Leu1423=	XP_016856295.1:p.Leu1423Pro
terminal uridylyltransferase 4 isoform X29	XP_011539401.1:p.Leu1401=	XP_011539401.1:p.Leu1401Pro
terminal uridylyltransferase 4 isoform X36	XP_016856297.1:p.Leu1383=	XP_016856297.1:p.Leu1383Pro
terminal uridylyltransferase 4 isoform X4	XP_047272281.1:p.Leu1499=	XP_047272281.1:p.Leu1499Pro
terminal uridylyltransferase 4 isoform X5	XP_047272282.1:p.Leu1498=	XP_047272282.1:p.Leu1498Pro
terminal uridylyltransferase 4 isoform X6	XP_047272283.1:p.Leu1494=	XP_047272283.1:p.Leu1494Pro
terminal uridylyltransferase 4 isoform X3	XP_047272280.1:p.Leu1494=	XP_047272280.1:p.Leu1494Pro
terminal uridylyltransferase 4 isoform X10	XP_047272288.1:p.Leu1472=	XP_047272288.1:p.Leu1472Pro
terminal uridylyltransferase 4 isoform X12	XP_047272295.1:p.Leu1470=	XP_047272295.1:p.Leu1470Pro
terminal uridylyltransferase 4 isoform X13	XP_047272296.1:p.Leu1469=	XP_047272296.1:p.Leu1469Pro
terminal uridylyltransferase 4 isoform X17	XP_047272305.1:p.Leu1465=	XP_047272305.1:p.Leu1465Pro
terminal uridylyltransferase 4 isoform X19	XP_047272307.1:p.Leu1460=	XP_047272307.1:p.Leu1460Pro
terminal uridylyltransferase 4 isoform X7	XP_047272285.1:p.Leu1471=	XP_047272285.1:p.Leu1471Pro
terminal uridylyltransferase 4 isoform X8	XP_047272286.1:p.Leu1470=	XP_047272286.1:p.Leu1470Pro
terminal uridylyltransferase 4 isoform X11	XP_047272290.1:p.Leu1465=	XP_047272290.1:p.Leu1465Pro
terminal uridylyltransferase 4 isoform X22	XP_047272320.1:p.Leu1434=	XP_047272320.1:p.Leu1434Pro
terminal uridylyltransferase 4 isoform X24	XP_047272327.1:p.Leu1433=	XP_047272327.1:p.Leu1433Pro
terminal uridylyltransferase 4 isoform X15	XP_047272303.1:p.Leu1460=	XP_047272303.1:p.Leu1460Pro
terminal uridylyltransferase 4 isoform X26	XP_047272336.1:p.Leu1429=	XP_047272336.1:p.Leu1429Pro
terminal uridylyltransferase 4 isoform X27	XP_047272337.1:p.Leu1427=	XP_047272337.1:p.Leu1427Pro
terminal uridylyltransferase 4 isoform X18	XP_047272306.1:p.Leu1456=	XP_047272306.1:p.Leu1456Pro
terminal uridylyltransferase 4 isoform X21	XP_047272311.1:p.Leu1434=	XP_047272311.1:p.Leu1434Pro
terminal uridylyltransferase 4 isoform X23	XP_047272325.1:p.Leu1427=	XP_047272325.1:p.Leu1427Pro
terminal uridylyltransferase 4 isoform X34	XP_047272350.1:p.Leu1394=	XP_047272350.1:p.Leu1394Pro
terminal uridylyltransferase 4 isoform X35	XP_047272354.1:p.Leu1390=	XP_047272354.1:p.Leu1390Pro
terminal uridylyltransferase 4 isoform X37	XP_047272362.1:p.Leu1389=	XP_047272362.1:p.Leu1389Pro
terminal uridylyltransferase 4 isoform X38	XP_047272365.1:p.Leu1387=	XP_047272365.1:p.Leu1387Pro
terminal uridylyltransferase 4 isoform X39	XP_047272367.1:p.Leu1385=	XP_047272367.1:p.Leu1385Pro
terminal uridylyltransferase 4 isoform X30	XP_047272344.1:p.Leu1399=	XP_047272344.1:p.Leu1399Pro
terminal uridylyltransferase 4 isoform X31	XP_047272345.1:p.Leu1396=	XP_047272345.1:p.Leu1396Pro
terminal uridylyltransferase 4 isoform X32	XP_047272348.1:p.Leu1390=	XP_047272348.1:p.Leu1390Pro
terminal uridylyltransferase 4 isoform X42	XP_047272372.1:p.Leu1358=	XP_047272372.1:p.Leu1358Pro
terminal uridylyltransferase 4 isoform X43	XP_047272373.1:p.Leu1350=	XP_047272373.1:p.Leu1350Pro
terminal uridylyltransferase 4 isoform X44	XP_047272377.1:p.Leu1345=	XP_047272377.1:p.Leu1345Pro
terminal uridylyltransferase 4 isoform X41	XP_047272369.1:p.Leu1363=	XP_047272369.1:p.Leu1363Pro
terminal uridylyltransferase 4 isoform X46	XP_047272384.1:p.Leu759=	XP_047272384.1:p.Leu759Pro

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 submission

No	Submitter	Submission ID	Date (Build)
1	GNOMAD	ss2731500215	Nov 08, 2017 (151)

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
ss2731500215	NC_000001.10:52896899:A:G	NC_000001.11:52431227:A:G	(self)

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

No publications for rs1481912801

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1481912801