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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.

rs1456517473

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr9:96551812 (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
G=0.000015 (4/264690, TOPMED)
G=0.000007 (1/140262, GnomAD)
G=0.00000 (0/14050, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
CDC14B : 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 30012 A=0.99997 G=0.00003 0.999933 0.0 6.7e-05 0
European Sub 19492 A=1.00000 G=0.00000 1.0 0.0 0.0 N/A
African Sub 7670 A=0.9999 G=0.0001 0.999739 0.0 0.000261 0
African Others Sub 298 A=1.000 G=0.000 1.0 0.0 0.0 N/A
African American Sub 7372 A=0.9999 G=0.0001 0.999729 0.0 0.000271 0
Asian Sub 112 A=1.000 G=0.000 1.0 0.0 0.0 N/A
East Asian Sub 86 A=1.00 G=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 26 A=1.00 G=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 A=1.000 G=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 A=1.000 G=0.000 1.0 0.0 0.0 N/A
South Asian Sub 98 A=1.00 G=0.00 1.0 0.0 0.0 N/A
Other Sub 1884 A=1.0000 G=0.0000 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 A=0.999985 G=0.000015
gnomAD - Genomes Global Study-wide 140262 A=0.999993 G=0.000007
gnomAD - Genomes European Sub 75950 A=1.00000 G=0.00000
gnomAD - Genomes African Sub 42042 A=0.99998 G=0.00002
gnomAD - Genomes American Sub 13662 A=1.00000 G=0.00000
gnomAD - Genomes Ashkenazi Jewish Sub 3322 A=1.0000 G=0.0000
gnomAD - Genomes East Asian Sub 3134 A=1.0000 G=0.0000
gnomAD - Genomes Other Sub 2152 A=1.0000 G=0.0000
Allele Frequency Aggregator Total Global 14050 A=1.00000 G=0.00000
Allele Frequency Aggregator European Sub 9690 A=1.0000 G=0.0000
Allele Frequency Aggregator African Sub 2898 A=1.0000 G=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 A=1.000 G=0.000
Allele Frequency Aggregator Other Sub 496 A=1.000 G=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 A=1.000 G=0.000
Allele Frequency Aggregator Asian Sub 112 A=1.000 G=0.000
Allele Frequency Aggregator South Asian Sub 98 A=1.00 G=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 9 NC_000009.12:g.96551812A>G
GRCh37.p13 chr 9 NC_000009.11:g.99314094A>G
Gene: CDC14B, cell division cycle 14B (minus strand)
Molecule type Change Amino acid[Codon] SO Term
CDC14B transcript variant 7 NM_001351570.1:c.412T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform 6 NP_001338499.1:p.Ser138Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant 2 NM_033331.4:c.481T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform 2 NP_201588.1:p.Ser161Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant 6 NM_001351569.2:c.370T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform 5 NP_001338498.1:p.Ser124Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant 3 NM_001077181.3:c.370T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform 3 NP_001070649.1:p.Ser124Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant 1 NM_003671.5:c.481T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform 1 NP_003662.1:p.Ser161Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant 4 NM_001351567.3:c.481T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform 4 NP_001338496.1:p.Ser161Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant 5 NM_001351568.3:c.370T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform 5 NP_001338497.1:p.Ser124Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant 8 NR_147239.2:n.946T>C N/A Non Coding Transcript Variant
CDC14B transcript variant X12 XM_017015241.3:c.351+1088…

XM_017015241.3:c.351+10881T>C

 		N/A Intron Variant
CDC14B transcript variant X23 XM_017015248.3:c.420+1088…

XM_017015248.3:c.420+10881T>C

 		N/A Intron Variant
CDC14B transcript variant X19 XM_047424000.1:c.420+1088…

XM_047424000.1:c.420+10881T>C

 		N/A Intron Variant
CDC14B transcript variant X25 XM_047424005.1:c.-70-9920…

XM_047424005.1:c.-70-9920T>C

 		N/A Intron Variant
CDC14B transcript variant X26 XM_047424006.1:c. N/A Genic Upstream Transcript Variant
CDC14B transcript variant X1 XM_017015240.3:c.412T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X1 XP_016870729.2:p.Ser138Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X2 XM_011519147.4:c.412T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X2 XP_011517449.2:p.Ser138Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X5 XM_011519148.4:c.412T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X3 XP_011517450.2:p.Ser138Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X6 XM_011519149.4:c.412T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X4 XP_011517451.2:p.Ser138Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X8 XM_011519151.4:c.412T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X5 XP_011517453.2:p.Ser138Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X9 XM_047423997.1:c.412T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X5 XP_047279953.1:p.Ser138Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X11 XM_011519153.4:c.412T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X6 XP_011517455.2:p.Ser138Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X13 XM_017015242.3:c.481T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X8 XP_016870731.1:p.Ser161Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X14 XM_011519156.4:c.463T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X9 XP_011517458.2:p.Ser155Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X15 XM_047423998.1:c.481T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X10 XP_047279954.1:p.Ser161Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X16 XM_017015244.3:c.370T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X11 XP_016870733.1:p.Ser124Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X17 XM_017015245.2:c.463T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X12 XP_016870734.1:p.Ser155Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X18 XM_047423999.1:c.481T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X13 XP_047279955.1:p.Ser161Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X20 XM_047424001.1:c.196T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X15 XP_047279957.1:p.Ser66Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X28 XM_047424002.1:c.196T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X15 XP_047279958.1:p.Ser66Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X21 XM_017015247.3:c.370T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X16 XP_016870736.1:p.Ser124Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X22 XM_047424003.1:c.196T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X17 XP_047279959.1:p.Ser66Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X24 XM_047424004.1:c.196T>C S [TCC] > P [CCC] Coding Sequence Variant
dual specificity protein phosphatase CDC14B isoform X19 XP_047279960.1:p.Ser66Pro S (Ser) > P (Pro) Missense Variant
CDC14B transcript variant X3 XR_929864.4:n.559T>C N/A Non Coding Transcript Variant
CDC14B transcript variant X4 XR_929865.4:n.559T>C N/A Non Coding Transcript Variant
CDC14B transcript variant X27 XR_007061366.1:n.559T>C N/A Non Coding Transcript Variant
CDC14B transcript variant X7 XR_001746406.3:n.559T>C N/A Non Coding Transcript Variant
CDC14B transcript variant X10 XR_007061367.1:n.559T>C 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 A= G
GRCh38.p14 chr 9 NC_000009.12:g.96551812= NC_000009.12:g.96551812A>G
GRCh37.p13 chr 9 NC_000009.11:g.99314094= NC_000009.11:g.99314094A>G
CDC14B transcript variant 1 NM_003671.5:c.481= NM_003671.5:c.481T>C
CDC14B transcript variant 1 NM_003671.4:c.481= NM_003671.4:c.481T>C
CDC14B transcript variant 1 NM_003671.3:c.481= NM_003671.3:c.481T>C
CDC14B transcript variant X14 XM_011519156.4:c.463= XM_011519156.4:c.463T>C
CDC14B transcript variant X15 XM_011519156.3:c.463= XM_011519156.3:c.463T>C
CDC14B transcript variant X15 XM_011519156.2:c.463= XM_011519156.2:c.463T>C
CDC14B transcript variant X16 XM_011519156.1:c.463= XM_011519156.1:c.463T>C
CDC14B transcript variant 2 NM_033331.4:c.481= NM_033331.4:c.481T>C
CDC14B transcript variant 2 NM_033331.3:c.481= NM_033331.3:c.481T>C
CDC14B transcript variant 2 NM_033331.2:c.481= NM_033331.2:c.481T>C
CDC14B transcript variant X5 XM_011519148.4:c.412= XM_011519148.4:c.412T>C
CDC14B transcript variant X5 XM_011519148.3:c.412= XM_011519148.3:c.412T>C
CDC14B transcript variant X5 XM_011519148.2:c.760= XM_011519148.2:c.760T>C
CDC14B transcript variant X6 XM_011519148.1:c.760= XM_011519148.1:c.760T>C
CDC14B transcript variant X11 XM_011519153.4:c.412= XM_011519153.4:c.412T>C
CDC14B transcript variant X12 XM_011519153.3:c.412= XM_011519153.3:c.412T>C
CDC14B transcript variant X12 XM_011519153.2:c.760= XM_011519153.2:c.760T>C
CDC14B transcript variant X13 XM_011519153.1:c.760= XM_011519153.1:c.760T>C
CDC14B transcript variant X3 XR_929864.4:n.559= XR_929864.4:n.559T>C
CDC14B transcript variant X3 XR_929864.3:n.414= XR_929864.3:n.414T>C
CDC14B transcript variant X3 XR_929864.2:n.880= XR_929864.2:n.880T>C
CDC14B transcript variant X3 XR_929864.1:n.775= XR_929864.1:n.775T>C
CDC14B transcript variant X2 XM_011519147.4:c.412= XM_011519147.4:c.412T>C
CDC14B transcript variant X2 XM_011519147.3:c.412= XM_011519147.3:c.412T>C
CDC14B transcript variant X2 XM_011519147.2:c.760= XM_011519147.2:c.760T>C
CDC14B transcript variant X2 XM_011519147.1:c.760= XM_011519147.1:c.760T>C
CDC14B transcript variant X4 XR_929865.4:n.559= XR_929865.4:n.559T>C
CDC14B transcript variant X4 XR_929865.3:n.414= XR_929865.3:n.414T>C
CDC14B transcript variant X4 XR_929865.2:n.880= XR_929865.2:n.880T>C
CDC14B transcript variant X4 XR_929865.1:n.775= XR_929865.1:n.775T>C
CDC14B transcript variant X8 XM_011519151.4:c.412= XM_011519151.4:c.412T>C
CDC14B transcript variant X10 XM_011519151.3:c.412= XM_011519151.3:c.412T>C
CDC14B transcript variant X10 XM_011519151.2:c.760= XM_011519151.2:c.760T>C
CDC14B transcript variant X11 XM_011519151.1:c.760= XM_011519151.1:c.760T>C
CDC14B transcript variant X6 XM_011519149.4:c.412= XM_011519149.4:c.412T>C
CDC14B transcript variant X6 XM_011519149.3:c.412= XM_011519149.3:c.412T>C
CDC14B transcript variant X6 XM_011519149.2:c.760= XM_011519149.2:c.760T>C
CDC14B transcript variant X7 XM_011519149.1:c.760= XM_011519149.1:c.760T>C
CDC14B transcript variant X13 XM_017015242.3:c.481= XM_017015242.3:c.481T>C
CDC14B transcript variant X14 XM_017015242.2:c.481= XM_017015242.2:c.481T>C
CDC14B transcript variant X14 XM_017015242.1:c.481= XM_017015242.1:c.481T>C
CDC14B transcript variant X1 XM_017015240.3:c.412= XM_017015240.3:c.412T>C
CDC14B transcript variant X1 XM_017015240.2:c.412= XM_017015240.2:c.412T>C
CDC14B transcript variant X1 XM_017015240.1:c.760= XM_017015240.1:c.760T>C
CDC14B transcript variant X16 XM_017015244.3:c.370= XM_017015244.3:c.370T>C
CDC14B transcript variant X17 XM_017015244.2:c.370= XM_017015244.2:c.370T>C
CDC14B transcript variant X19 XM_017015244.1:c.370= XM_017015244.1:c.370T>C
CDC14B transcript variant X21 XM_017015247.3:c.370= XM_017015247.3:c.370T>C
CDC14B transcript variant X22 XM_017015247.2:c.370= XM_017015247.2:c.370T>C
CDC14B transcript variant X26 XM_017015247.1:c.370= XM_017015247.1:c.370T>C
CDC14B transcript variant 3 NM_001077181.3:c.370= NM_001077181.3:c.370T>C
CDC14B transcript variant 3 NM_001077181.2:c.370= NM_001077181.2:c.370T>C
CDC14B transcript variant 3 NM_001077181.1:c.370= NM_001077181.1:c.370T>C
CDC14B transcript variant 4 NM_001351567.3:c.481= NM_001351567.3:c.481T>C
CDC14B transcript variant 4 NM_001351567.2:c.481= NM_001351567.2:c.481T>C
CDC14B transcript variant 4 NM_001351567.1:c.481= NM_001351567.1:c.481T>C
CDC14B transcript variant 5 NM_001351568.3:c.370= NM_001351568.3:c.370T>C
CDC14B transcript variant 5 NM_001351568.2:c.370= NM_001351568.2:c.370T>C
CDC14B transcript variant 5 NM_001351568.1:c.370= NM_001351568.1:c.370T>C
CDC14B transcript variant X7 XR_001746406.3:n.559= XR_001746406.3:n.559T>C
CDC14B transcript variant X7 XR_001746406.2:n.414= XR_001746406.2:n.414T>C
CDC14B transcript variant X7 XR_001746406.1:n.877= XR_001746406.1:n.877T>C
CDC14B transcript variant 8 NR_147239.2:n.946= NR_147239.2:n.946T>C
CDC14B transcript variant 8 NR_147239.1:n.933= NR_147239.1:n.933T>C
CDC14B transcript variant 6 NM_001351569.2:c.370= NM_001351569.2:c.370T>C
CDC14B transcript variant 6 NM_001351569.1:c.370= NM_001351569.1:c.370T>C
CDC14B transcript variant X17 XM_017015245.2:c.463= XM_017015245.2:c.463T>C
CDC14B transcript variant X19 XM_017015245.1:c.463= XM_017015245.1:c.463T>C
CDC14B transcript variant X20 XM_047424001.1:c.196= XM_047424001.1:c.196T>C
CDC14B transcript variant X22 XM_047424003.1:c.196= XM_047424003.1:c.196T>C
CDC14B transcript variant X28 XM_047424002.1:c.196= XM_047424002.1:c.196T>C
CDC14B transcript variant X24 XM_047424004.1:c.196= XM_047424004.1:c.196T>C
CDC14B transcript variant 7 NM_001351570.1:c.412= NM_001351570.1:c.412T>C
CDC14B transcript variant 3 NM_033332.1:c.481= NM_033332.1:c.481T>C
CDC14B transcript variant X10 XR_007061367.1:n.559= XR_007061367.1:n.559T>C
CDC14B transcript variant X27 XR_007061366.1:n.559= XR_007061366.1:n.559T>C
CDC14B transcript variant X18 XM_047423999.1:c.481= XM_047423999.1:c.481T>C
CDC14B transcript variant X15 XM_047423998.1:c.481= XM_047423998.1:c.481T>C
CDC14B transcript variant X9 XM_047423997.1:c.412= XM_047423997.1:c.412T>C
dual specificity protein phosphatase CDC14B isoform 1 NP_003662.1:p.Ser161= NP_003662.1:p.Ser161Pro
dual specificity protein phosphatase CDC14B isoform X9 XP_011517458.2:p.Ser155= XP_011517458.2:p.Ser155Pro
dual specificity protein phosphatase CDC14B isoform 2 NP_201588.1:p.Ser161= NP_201588.1:p.Ser161Pro
dual specificity protein phosphatase CDC14B isoform X3 XP_011517450.2:p.Ser138= XP_011517450.2:p.Ser138Pro
dual specificity protein phosphatase CDC14B isoform X6 XP_011517455.2:p.Ser138= XP_011517455.2:p.Ser138Pro
dual specificity protein phosphatase CDC14B isoform X2 XP_011517449.2:p.Ser138= XP_011517449.2:p.Ser138Pro
dual specificity protein phosphatase CDC14B isoform X5 XP_011517453.2:p.Ser138= XP_011517453.2:p.Ser138Pro
dual specificity protein phosphatase CDC14B isoform X4 XP_011517451.2:p.Ser138= XP_011517451.2:p.Ser138Pro
dual specificity protein phosphatase CDC14B isoform X8 XP_016870731.1:p.Ser161= XP_016870731.1:p.Ser161Pro
dual specificity protein phosphatase CDC14B isoform X1 XP_016870729.2:p.Ser138= XP_016870729.2:p.Ser138Pro
dual specificity protein phosphatase CDC14B isoform X11 XP_016870733.1:p.Ser124= XP_016870733.1:p.Ser124Pro
dual specificity protein phosphatase CDC14B isoform X16 XP_016870736.1:p.Ser124= XP_016870736.1:p.Ser124Pro
dual specificity protein phosphatase CDC14B isoform 3 NP_001070649.1:p.Ser124= NP_001070649.1:p.Ser124Pro
dual specificity protein phosphatase CDC14B isoform 4 NP_001338496.1:p.Ser161= NP_001338496.1:p.Ser161Pro
dual specificity protein phosphatase CDC14B isoform 5 NP_001338497.1:p.Ser124= NP_001338497.1:p.Ser124Pro
dual specificity protein phosphatase CDC14B isoform 5 NP_001338498.1:p.Ser124= NP_001338498.1:p.Ser124Pro
dual specificity protein phosphatase CDC14B isoform X12 XP_016870734.1:p.Ser155= XP_016870734.1:p.Ser155Pro
dual specificity protein phosphatase CDC14B isoform X15 XP_047279957.1:p.Ser66= XP_047279957.1:p.Ser66Pro
dual specificity protein phosphatase CDC14B isoform X17 XP_047279959.1:p.Ser66= XP_047279959.1:p.Ser66Pro
dual specificity protein phosphatase CDC14B isoform X15 XP_047279958.1:p.Ser66= XP_047279958.1:p.Ser66Pro
dual specificity protein phosphatase CDC14B isoform X19 XP_047279960.1:p.Ser66= XP_047279960.1:p.Ser66Pro
dual specificity protein phosphatase CDC14B isoform 6 NP_001338499.1:p.Ser138= NP_001338499.1:p.Ser138Pro
dual specificity protein phosphatase CDC14B isoform X13 XP_047279955.1:p.Ser161= XP_047279955.1:p.Ser161Pro
dual specificity protein phosphatase CDC14B isoform X10 XP_047279954.1:p.Ser161= XP_047279954.1:p.Ser161Pro
dual specificity protein phosphatase CDC14B isoform X5 XP_047279953.1:p.Ser138= XP_047279953.1:p.Ser138Pro
CDC14B transcript variant X12 XM_017015241.3:c.351+10881= XM_017015241.3:c.351+10881T>C
CDC14B transcript variant X23 XM_017015248.3:c.420+10881= XM_017015248.3:c.420+10881T>C
CDC14B transcript variant X19 XM_047424000.1:c.420+10881= XM_047424000.1:c.420+10881T>C
CDC14B transcript variant X25 XM_047424005.1:c.-70-9920= XM_047424005.1:c.-70-9920T>C
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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 ss4206140726 Apr 26, 2021 (155)
2 TOPMED ss4828913949 Apr 26, 2021 (155)
3 gnomAD - Genomes NC_000009.12 - 96551812 Apr 26, 2021 (155)
4 TopMed NC_000009.12 - 96551812 Apr 26, 2021 (155)
5 ALFA NC_000009.12 - 96551812 Apr 26, 2021 (155)
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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
332140102, 666291510, 12845100567, ss4206140726, ss4828913949 NC_000009.12:96551811:A:G NC_000009.12:96551811:A:G (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 rs1456517473

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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
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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