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.

rs1490641229

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr3:15724406 (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
C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.000004 (1/264690, TOPMED)
T=0.00000 (0/10680, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ANKRD28 : Synonymous 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 10680 C=1.00000 T=0.00000 1.0 0.0 0.0 N/A
European Sub 6962 C=1.0000 T=0.0000 1.0 0.0 0.0 N/A
African Sub 2294 C=1.0000 T=0.0000 1.0 0.0 0.0 N/A
African Others Sub 84 C=1.00 T=0.00 1.0 0.0 0.0 N/A
African American Sub 2210 C=1.0000 T=0.0000 1.0 0.0 0.0 N/A
Asian Sub 108 C=1.000 T=0.000 1.0 0.0 0.0 N/A
East Asian Sub 84 C=1.00 T=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 24 C=1.00 T=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 C=1.000 T=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 C=1.000 T=0.000 1.0 0.0 0.0 N/A
South Asian Sub 94 C=1.00 T=0.00 1.0 0.0 0.0 N/A
Other Sub 466 C=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
TopMed Global Study-wide 264690 C=0.999996 T=0.000004
Allele Frequency Aggregator Total Global 10680 C=1.00000 T=0.00000
Allele Frequency Aggregator European Sub 6962 C=1.0000 T=0.0000
Allele Frequency Aggregator African Sub 2294 C=1.0000 T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 C=1.000 T=0.000
Allele Frequency Aggregator Other Sub 466 C=1.000 T=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 C=1.000 T=0.000
Allele Frequency Aggregator Asian Sub 108 C=1.000 T=0.000
Allele Frequency Aggregator South Asian Sub 94 C=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 3 NC_000003.12:g.15724406C>T
GRCh37.p13 chr 3 NC_000003.11:g.15765913C>T
Gene: ANKRD28, ankyrin repeat domain 28 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ANKRD28 transcript variant 11 NM_001349284.2:c. N/A Genic Downstream Transcript Variant
ANKRD28 transcript variant 12 NM_001349285.2:c. N/A Genic Downstream Transcript Variant
ANKRD28 transcript variant 2 NM_001195098.1:c.207G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform b NP_001182027.1:p.Lys69= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant 7 NM_001349280.1:c.501G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform f NP_001336209.1:p.Lys167= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant 1 NM_015199.4:c.669G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform a NP_056014.2:p.Lys223= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant 5 NM_001349278.2:c.759G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform d NP_001336207.1:p.Lys253= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant 3 NM_001195099.2:c.207G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform b NP_001182028.1:p.Lys69= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant 9 NM_001349282.2:c.501G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform f NP_001336211.1:p.Lys167= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant 4 NM_001349277.2:c.768G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform c NP_001336206.1:p.Lys256= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant 6 NM_001349279.2:c.660G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform e NP_001336208.1:p.Lys220= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant 10 NM_001349283.2:c.207G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform b NP_001336212.1:p.Lys69= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant 8 NM_001349281.2:c.501G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform f NP_001336210.1:p.Lys167= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant 13 NR_146111.1:n.785G>A N/A Non Coding Transcript Variant
ANKRD28 transcript variant 14 NR_146112.2:n.2217G>A N/A Non Coding Transcript Variant
ANKRD28 transcript variant X2 XM_024453418.2:c.711G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X1 XP_024309186.1:p.Lys237= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X3 XM_024453419.2:c.702G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X2 XP_024309187.1:p.Lys234= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X5 XM_047447800.1:c.768G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X3 XP_047303756.1:p.Lys256= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X6 XM_011533542.4:c.585G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X4 XP_011531844.1:p.Lys195= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X7 XM_047447801.1:c.759G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X5 XP_047303757.1:p.Lys253= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X8 XM_047447802.1:c.567G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X6 XP_047303758.1:p.Lys189= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X9 XM_047447803.1:c.558G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X7 XP_047303759.1:p.Lys186= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X10 XM_047447804.1:c.501G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X8 XP_047303760.1:p.Lys167= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X11 XM_047447805.1:c.501G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X8 XP_047303761.1:p.Lys167= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X12 XM_024453424.2:c.501G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X8 XP_024309192.1:p.Lys167= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X13 XM_011533547.4:c.501G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X8 XP_011531849.1:p.Lys167= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X14 XM_024453422.2:c.501G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X8 XP_024309190.1:p.Lys167= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X15 XM_047447806.1:c.669G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X9 XP_047303762.1:p.Lys223= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X16 XM_047447807.1:c.483G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X10 XP_047303763.1:p.Lys161= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X17 XM_047447808.1:c.660G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X11 XP_047303764.1:p.Lys220= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X18 XM_047447809.1:c.468G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X12 XP_047303765.1:p.Lys156= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X19 XM_047447810.1:c.459G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X13 XP_047303766.1:p.Lys153= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X20 XM_047447811.1:c.768G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X14 XP_047303767.1:p.Lys256= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X21 XM_047447812.1:c.768G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X15 XP_047303768.1:p.Lys256= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X22 XM_047447813.1:c.207G>A K [AAG] > K [AAA] Coding Sequence Variant
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X16 XP_047303769.1:p.Lys69= K (Lys) > K (Lys) Synonymous Variant
ANKRD28 transcript variant X1 XR_007095652.1:n.2226G>A N/A Non Coding Transcript Variant
ANKRD28 transcript variant X4 XR_007095653.1:n.1080G>A 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 C= T
GRCh38.p14 chr 3 NC_000003.12:g.15724406= NC_000003.12:g.15724406C>T
GRCh37.p13 chr 3 NC_000003.11:g.15765913= NC_000003.11:g.15765913C>T
ANKRD28 transcript variant X13 XM_011533547.4:c.501= XM_011533547.4:c.501G>A
ANKRD28 transcript variant X9 XM_011533547.3:c.501= XM_011533547.3:c.501G>A
ANKRD28 transcript variant X10 XM_011533547.2:c.501= XM_011533547.2:c.501G>A
ANKRD28 transcript variant X9 XM_011533547.1:c.501= XM_011533547.1:c.501G>A
ANKRD28 transcript variant 1 NM_015199.4:c.669= NM_015199.4:c.669G>A
ANKRD28 transcript variant 1 NM_015199.3:c.669= NM_015199.3:c.669G>A
ANKRD28 transcript variant X6 XM_011533542.4:c.585= XM_011533542.4:c.585G>A
ANKRD28 transcript variant X7 XM_011533542.3:c.585= XM_011533542.3:c.585G>A
ANKRD28 transcript variant X6 XM_011533542.2:c.585= XM_011533542.2:c.585G>A
ANKRD28 transcript variant X4 XM_011533542.1:c.585= XM_011533542.1:c.585G>A
ANKRD28 transcript variant 4 NM_001349277.2:c.768= NM_001349277.2:c.768G>A
ANKRD28 transcript variant 4 NM_001349277.1:c.768= NM_001349277.1:c.768G>A
ANKRD28 transcript variant 5 NM_001349278.2:c.759= NM_001349278.2:c.759G>A
ANKRD28 transcript variant 5 NM_001349278.1:c.759= NM_001349278.1:c.759G>A
ANKRD28 transcript variant 10 NM_001349283.2:c.207= NM_001349283.2:c.207G>A
ANKRD28 transcript variant 10 NM_001349283.1:c.207= NM_001349283.1:c.207G>A
ANKRD28 transcript variant 9 NM_001349282.2:c.501= NM_001349282.2:c.501G>A
ANKRD28 transcript variant 9 NM_001349282.1:c.501= NM_001349282.1:c.501G>A
ANKRD28 transcript variant 8 NM_001349281.2:c.501= NM_001349281.2:c.501G>A
ANKRD28 transcript variant 8 NM_001349281.1:c.501= NM_001349281.1:c.501G>A
ANKRD28 transcript variant X2 XM_024453418.2:c.711= XM_024453418.2:c.711G>A
ANKRD28 transcript variant X1 XM_024453418.1:c.711= XM_024453418.1:c.711G>A
ANKRD28 transcript variant X3 XM_024453419.2:c.702= XM_024453419.2:c.702G>A
ANKRD28 transcript variant X3 XM_024453419.1:c.702= XM_024453419.1:c.702G>A
ANKRD28 transcript variant 6 NM_001349279.2:c.660= NM_001349279.2:c.660G>A
ANKRD28 transcript variant 6 NM_001349279.1:c.660= NM_001349279.1:c.660G>A
ANKRD28 transcript variant X14 XM_024453422.2:c.501= XM_024453422.2:c.501G>A
ANKRD28 transcript variant X10 XM_024453422.1:c.501= XM_024453422.1:c.501G>A
ANKRD28 transcript variant X12 XM_024453424.2:c.501= XM_024453424.2:c.501G>A
ANKRD28 transcript variant X12 XM_024453424.1:c.501= XM_024453424.1:c.501G>A
ANKRD28 transcript variant 3 NM_001195099.2:c.207= NM_001195099.2:c.207G>A
ANKRD28 transcript variant 3 NM_001195099.1:c.207= NM_001195099.1:c.207G>A
ANKRD28 transcript variant 14 NR_146112.2:n.2217= NR_146112.2:n.2217G>A
ANKRD28 transcript variant 14 NR_146112.1:n.2422= NR_146112.1:n.2422G>A
ANKRD28 transcript variant X8 XM_047447802.1:c.567= XM_047447802.1:c.567G>A
ANKRD28 transcript variant X9 XM_047447803.1:c.558= XM_047447803.1:c.558G>A
ANKRD28 transcript variant X19 XM_047447810.1:c.459= XM_047447810.1:c.459G>A
ANKRD28 transcript variant X16 XM_047447807.1:c.483= XM_047447807.1:c.483G>A
ANKRD28 transcript variant X18 XM_047447809.1:c.468= XM_047447809.1:c.468G>A
ANKRD28 transcript variant 2 NM_001195098.1:c.207= NM_001195098.1:c.207G>A
ANKRD28 transcript variant X10 XM_047447804.1:c.501= XM_047447804.1:c.501G>A
ANKRD28 transcript variant X11 XM_047447805.1:c.501= XM_047447805.1:c.501G>A
ANKRD28 transcript variant 7 NM_001349280.1:c.501= NM_001349280.1:c.501G>A
ANKRD28 transcript variant X5 XM_047447800.1:c.768= XM_047447800.1:c.768G>A
ANKRD28 transcript variant X7 XM_047447801.1:c.759= XM_047447801.1:c.759G>A
ANKRD28 transcript variant X22 XM_047447813.1:c.207= XM_047447813.1:c.207G>A
ANKRD28 transcript variant X1 XR_007095652.1:n.2226= XR_007095652.1:n.2226G>A
ANKRD28 transcript variant X17 XM_047447808.1:c.660= XM_047447808.1:c.660G>A
ANKRD28 transcript variant X15 XM_047447806.1:c.669= XM_047447806.1:c.669G>A
ANKRD28 transcript variant X4 XR_007095653.1:n.1080= XR_007095653.1:n.1080G>A
ANKRD28 transcript variant 13 NR_146111.1:n.785= NR_146111.1:n.785G>A
ANKRD28 transcript variant X20 XM_047447811.1:c.768= XM_047447811.1:c.768G>A
ANKRD28 transcript variant X21 XM_047447812.1:c.768= XM_047447812.1:c.768G>A
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X8 XP_011531849.1:p.Lys167= XP_011531849.1:p.Lys167=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform a NP_056014.2:p.Lys223= NP_056014.2:p.Lys223=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X4 XP_011531844.1:p.Lys195= XP_011531844.1:p.Lys195=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform c NP_001336206.1:p.Lys256= NP_001336206.1:p.Lys256=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform d NP_001336207.1:p.Lys253= NP_001336207.1:p.Lys253=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform b NP_001336212.1:p.Lys69= NP_001336212.1:p.Lys69=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform f NP_001336211.1:p.Lys167= NP_001336211.1:p.Lys167=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform f NP_001336210.1:p.Lys167= NP_001336210.1:p.Lys167=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X1 XP_024309186.1:p.Lys237= XP_024309186.1:p.Lys237=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X2 XP_024309187.1:p.Lys234= XP_024309187.1:p.Lys234=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform e NP_001336208.1:p.Lys220= NP_001336208.1:p.Lys220=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X8 XP_024309190.1:p.Lys167= XP_024309190.1:p.Lys167=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X8 XP_024309192.1:p.Lys167= XP_024309192.1:p.Lys167=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform b NP_001182028.1:p.Lys69= NP_001182028.1:p.Lys69=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X6 XP_047303758.1:p.Lys189= XP_047303758.1:p.Lys189=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X7 XP_047303759.1:p.Lys186= XP_047303759.1:p.Lys186=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X13 XP_047303766.1:p.Lys153= XP_047303766.1:p.Lys153=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X10 XP_047303763.1:p.Lys161= XP_047303763.1:p.Lys161=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X12 XP_047303765.1:p.Lys156= XP_047303765.1:p.Lys156=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform b NP_001182027.1:p.Lys69= NP_001182027.1:p.Lys69=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X8 XP_047303760.1:p.Lys167= XP_047303760.1:p.Lys167=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X8 XP_047303761.1:p.Lys167= XP_047303761.1:p.Lys167=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform f NP_001336209.1:p.Lys167= NP_001336209.1:p.Lys167=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X3 XP_047303756.1:p.Lys256= XP_047303756.1:p.Lys256=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X5 XP_047303757.1:p.Lys253= XP_047303757.1:p.Lys253=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X16 XP_047303769.1:p.Lys69= XP_047303769.1:p.Lys69=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X11 XP_047303764.1:p.Lys220= XP_047303764.1:p.Lys220=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X9 XP_047303762.1:p.Lys223= XP_047303762.1:p.Lys223=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X14 XP_047303767.1:p.Lys256= XP_047303767.1:p.Lys256=
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A isoform X15 XP_047303768.1:p.Lys256= XP_047303768.1:p.Lys256=
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, 2 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2733577488 Nov 08, 2017 (151)
2 TOPMED ss4555315681 Apr 27, 2021 (155)
3 TopMed NC_000003.12 - 15724406 Apr 27, 2021 (155)
4 ALFA NC_000003.12 - 15724406 Apr 27, 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
ss2733577488 NC_000003.11:15765912:C:T NC_000003.12:15724405:C:T (self)
392693236, 900929760, ss4555315681 NC_000003.12:15724405:C:T NC_000003.12:15724405:C: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 rs1490641229

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