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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.

rs1488735423

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr3:51310266 (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>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.000004 (1/264690, TOPMED)
C=0.000007 (1/140190, GnomAD)
C=0.00000 (0/14050, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
DOCK3 : 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 C=0.00000 1.0 0.0 0.0 N/A
European Sub 9690 A=1.0000 C=0.0000 1.0 0.0 0.0 N/A
African Sub 2898 A=1.0000 C=0.0000 1.0 0.0 0.0 N/A
African Others Sub 114 A=1.000 C=0.000 1.0 0.0 0.0 N/A
African American Sub 2784 A=1.0000 C=0.0000 1.0 0.0 0.0 N/A
Asian Sub 112 A=1.000 C=0.000 1.0 0.0 0.0 N/A
East Asian Sub 86 A=1.00 C=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 26 A=1.00 C=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 A=1.000 C=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 A=1.000 C=0.000 1.0 0.0 0.0 N/A
South Asian Sub 98 A=1.00 C=0.00 1.0 0.0 0.0 N/A
Other Sub 496 A=1.000 C=0.000 1.0 0.0 0.0 N/A


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 264690 A=0.999996 C=0.000004
gnomAD - Genomes Global Study-wide 140190 A=0.999993 C=0.000007
gnomAD - Genomes European Sub 75904 A=1.00000 C=0.00000
gnomAD - Genomes African Sub 42022 A=0.99998 C=0.00002
gnomAD - Genomes American Sub 13656 A=1.00000 C=0.00000
gnomAD - Genomes Ashkenazi Jewish Sub 3324 A=1.0000 C=0.0000
gnomAD - Genomes East Asian Sub 3130 A=1.0000 C=0.0000
gnomAD - Genomes Other Sub 2154 A=1.0000 C=0.0000
Allele Frequency Aggregator Total Global 14050 A=1.00000 C=0.00000
Allele Frequency Aggregator European Sub 9690 A=1.0000 C=0.0000
Allele Frequency Aggregator African Sub 2898 A=1.0000 C=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 A=1.000 C=0.000
Allele Frequency Aggregator Other Sub 496 A=1.000 C=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 A=1.000 C=0.000
Allele Frequency Aggregator Asian Sub 112 A=1.000 C=0.000
Allele Frequency Aggregator South Asian Sub 98 A=1.00 C=0.00
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 3 NC_000003.12:g.51310266A>C
GRCh37.p13 chr 3 NC_000003.11:g.51347697A>C
DOCK3 RefSeqGene NG_028012.2:g.640026A>C
Gene: DOCK3, dedicator of cytokinesis 3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
DOCK3 transcript NM_004947.5:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 NP_004938.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X1 XM_005264914.4:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X1 XP_005264971.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X2 XM_005264915.4:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X2 XP_005264972.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X3 XM_005264916.5:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X3 XP_005264973.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X4 XM_005264917.4:c.2915A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X4 XP_005264974.1:p.Asn972Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X5 XM_006713008.4:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X5 XP_006713071.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X6 XM_047447595.1:c.2915A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X6 XP_047303551.1:p.Asn972Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X7 XM_047447596.1:c.2915A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X7 XP_047303552.1:p.Asn972Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X8 XM_006713009.4:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X8 XP_006713072.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X9 XM_017005825.3:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X9 XP_016861314.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X10 XM_005264918.5:c.2810A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X10 XP_005264975.1:p.Asn937Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X11 XM_047447597.1:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X11 XP_047303553.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X12 XM_047447598.1:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X12 XP_047303554.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X13 XM_047447599.1:c.2810A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X13 XP_047303555.1:p.Asn937Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X14 XM_047447600.1:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X14 XP_047303556.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X15 XM_047447601.1:c.2915A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X15 XP_047303557.1:p.Asn972Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X16 XM_047447602.1:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X16 XP_047303558.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X17 XM_047447603.1:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X17 XP_047303559.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X18 XM_017005826.3:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X18 XP_016861315.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X19 XM_006713010.4:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X19 XP_006713073.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X20 XM_047447604.1:c.2957A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X20 XP_047303560.1:p.Asn986Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X21 XM_047447605.1:c.2603A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X21 XP_047303561.1:p.Asn868Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X22 XM_017005827.3:c.2144A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X22 XP_016861316.1:p.Asn715Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X23 XM_011533441.4:c.1922A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X23 XP_011531743.1:p.Asn641Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X24 XM_047447606.1:c.1796A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X24 XP_047303562.1:p.Asn599Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X25 XM_011533443.3:c.269A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X25 XP_011531745.1:p.Asn90Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X26 XM_011533444.3:c.269A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X25 XP_011531746.1:p.Asn90Thr N (Asn) > T (Thr) Missense Variant
DOCK3 transcript variant X27 XM_011533445.3:c.95A>C N [AAC] > T [ACC] Coding Sequence Variant
dedicator of cytokinesis protein 3 isoform X26 XP_011531747.1:p.Asn32Thr N (Asn) > T (Thr) 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= C
GRCh38.p14 chr 3 NC_000003.12:g.51310266= NC_000003.12:g.51310266A>C
GRCh37.p13 chr 3 NC_000003.11:g.51347697= NC_000003.11:g.51347697A>C
DOCK3 RefSeqGene NG_028012.2:g.640026= NG_028012.2:g.640026A>C
DOCK3 transcript NM_004947.5:c.2957= NM_004947.5:c.2957A>C
DOCK3 transcript NM_004947.4:c.2957= NM_004947.4:c.2957A>C
DOCK3 transcript variant X3 XM_005264916.5:c.2957= XM_005264916.5:c.2957A>C
DOCK3 transcript variant X3 XM_005264916.4:c.2957= XM_005264916.4:c.2957A>C
DOCK3 transcript variant X3 XM_005264916.3:c.2957= XM_005264916.3:c.2957A>C
DOCK3 transcript variant X3 XM_005264916.2:c.2957= XM_005264916.2:c.2957A>C
DOCK3 transcript variant X3 XM_005264916.1:c.2957= XM_005264916.1:c.2957A>C
DOCK3 transcript variant X10 XM_005264918.5:c.2810= XM_005264918.5:c.2810A>C
DOCK3 transcript variant X8 XM_005264918.4:c.2810= XM_005264918.4:c.2810A>C
DOCK3 transcript variant X8 XM_005264918.3:c.2810= XM_005264918.3:c.2810A>C
DOCK3 transcript variant X7 XM_005264918.2:c.2810= XM_005264918.2:c.2810A>C
DOCK3 transcript variant X5 XM_005264918.1:c.2810= XM_005264918.1:c.2810A>C
DOCK3 transcript variant X23 XM_011533441.4:c.1922= XM_011533441.4:c.1922A>C
DOCK3 transcript variant X12 XM_011533441.3:c.1922= XM_011533441.3:c.1922A>C
DOCK3 transcript variant X12 XM_011533441.2:c.1922= XM_011533441.2:c.1922A>C
DOCK3 transcript variant X9 XM_011533441.1:c.1922= XM_011533441.1:c.1922A>C
DOCK3 transcript variant X1 XM_005264914.4:c.2957= XM_005264914.4:c.2957A>C
DOCK3 transcript variant X1 XM_005264914.3:c.2957= XM_005264914.3:c.2957A>C
DOCK3 transcript variant X1 XM_005264914.2:c.2957= XM_005264914.2:c.2957A>C
DOCK3 transcript variant X1 XM_005264914.1:c.2957= XM_005264914.1:c.2957A>C
DOCK3 transcript variant X2 XM_005264915.4:c.2957= XM_005264915.4:c.2957A>C
DOCK3 transcript variant X2 XM_005264915.3:c.2957= XM_005264915.3:c.2957A>C
DOCK3 transcript variant X2 XM_005264915.2:c.2957= XM_005264915.2:c.2957A>C
DOCK3 transcript variant X2 XM_005264915.1:c.2957= XM_005264915.1:c.2957A>C
DOCK3 transcript variant X4 XM_005264917.4:c.2915= XM_005264917.4:c.2915A>C
DOCK3 transcript variant X4 XM_005264917.3:c.2915= XM_005264917.3:c.2915A>C
DOCK3 transcript variant X4 XM_005264917.2:c.2915= XM_005264917.2:c.2915A>C
DOCK3 transcript variant X4 XM_005264917.1:c.2915= XM_005264917.1:c.2915A>C
DOCK3 transcript variant X5 XM_006713008.4:c.2957= XM_006713008.4:c.2957A>C
DOCK3 transcript variant X5 XM_006713008.3:c.2957= XM_006713008.3:c.2957A>C
DOCK3 transcript variant X5 XM_006713008.2:c.2957= XM_006713008.2:c.2957A>C
DOCK3 transcript variant X6 XM_006713008.1:c.2957= XM_006713008.1:c.2957A>C
DOCK3 transcript variant X8 XM_006713009.4:c.2957= XM_006713009.4:c.2957A>C
DOCK3 transcript variant X6 XM_006713009.3:c.2957= XM_006713009.3:c.2957A>C
DOCK3 transcript variant X6 XM_006713009.2:c.2957= XM_006713009.2:c.2957A>C
DOCK3 transcript variant X7 XM_006713009.1:c.2957= XM_006713009.1:c.2957A>C
DOCK3 transcript variant X19 XM_006713010.4:c.2957= XM_006713010.4:c.2957A>C
DOCK3 transcript variant X10 XM_006713010.3:c.2957= XM_006713010.3:c.2957A>C
DOCK3 transcript variant X8 XM_006713010.2:c.2957= XM_006713010.2:c.2957A>C
DOCK3 transcript variant X8 XM_006713010.1:c.2957= XM_006713010.1:c.2957A>C
DOCK3 transcript variant X9 XM_017005825.3:c.2957= XM_017005825.3:c.2957A>C
DOCK3 transcript variant X7 XM_017005825.2:c.2957= XM_017005825.2:c.2957A>C
DOCK3 transcript variant X7 XM_017005825.1:c.2957= XM_017005825.1:c.2957A>C
DOCK3 transcript variant X18 XM_017005826.3:c.2957= XM_017005826.3:c.2957A>C
DOCK3 transcript variant X9 XM_017005826.2:c.2957= XM_017005826.2:c.2957A>C
DOCK3 transcript variant X9 XM_017005826.1:c.2957= XM_017005826.1:c.2957A>C
DOCK3 transcript variant X22 XM_017005827.3:c.2144= XM_017005827.3:c.2144A>C
DOCK3 transcript variant X11 XM_017005827.2:c.2144= XM_017005827.2:c.2144A>C
DOCK3 transcript variant X11 XM_017005827.1:c.2144= XM_017005827.1:c.2144A>C
DOCK3 transcript variant X25 XM_011533443.3:c.269= XM_011533443.3:c.269A>C
DOCK3 transcript variant X13 XM_011533443.2:c.269= XM_011533443.2:c.269A>C
DOCK3 transcript variant X11 XM_011533443.1:c.269= XM_011533443.1:c.269A>C
DOCK3 transcript variant X27 XM_011533445.3:c.95= XM_011533445.3:c.95A>C
DOCK3 transcript variant X15 XM_011533445.2:c.95= XM_011533445.2:c.95A>C
DOCK3 transcript variant X13 XM_011533445.1:c.95= XM_011533445.1:c.95A>C
DOCK3 transcript variant X26 XM_011533444.3:c.269= XM_011533444.3:c.269A>C
DOCK3 transcript variant X14 XM_011533444.2:c.269= XM_011533444.2:c.269A>C
DOCK3 transcript variant X12 XM_011533444.1:c.269= XM_011533444.1:c.269A>C
DOCK3 transcript variant X6 XM_047447595.1:c.2915= XM_047447595.1:c.2915A>C
DOCK3 transcript variant X7 XM_047447596.1:c.2915= XM_047447596.1:c.2915A>C
DOCK3 transcript variant X11 XM_047447597.1:c.2957= XM_047447597.1:c.2957A>C
DOCK3 transcript variant X12 XM_047447598.1:c.2957= XM_047447598.1:c.2957A>C
DOCK3 transcript variant X13 XM_047447599.1:c.2810= XM_047447599.1:c.2810A>C
DOCK3 transcript variant X14 XM_047447600.1:c.2957= XM_047447600.1:c.2957A>C
DOCK3 transcript variant X16 XM_047447602.1:c.2957= XM_047447602.1:c.2957A>C
DOCK3 transcript variant X15 XM_047447601.1:c.2915= XM_047447601.1:c.2915A>C
DOCK3 transcript variant X17 XM_047447603.1:c.2957= XM_047447603.1:c.2957A>C
DOCK3 transcript variant X21 XM_047447605.1:c.2603= XM_047447605.1:c.2603A>C
DOCK3 transcript variant X20 XM_047447604.1:c.2957= XM_047447604.1:c.2957A>C
DOCK3 transcript variant X24 XM_047447606.1:c.1796= XM_047447606.1:c.1796A>C
dedicator of cytokinesis protein 3 NP_004938.1:p.Asn986= NP_004938.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X3 XP_005264973.1:p.Asn986= XP_005264973.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X10 XP_005264975.1:p.Asn937= XP_005264975.1:p.Asn937Thr
dedicator of cytokinesis protein 3 isoform X23 XP_011531743.1:p.Asn641= XP_011531743.1:p.Asn641Thr
dedicator of cytokinesis protein 3 isoform X1 XP_005264971.1:p.Asn986= XP_005264971.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X2 XP_005264972.1:p.Asn986= XP_005264972.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X4 XP_005264974.1:p.Asn972= XP_005264974.1:p.Asn972Thr
dedicator of cytokinesis protein 3 isoform X5 XP_006713071.1:p.Asn986= XP_006713071.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X8 XP_006713072.1:p.Asn986= XP_006713072.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X19 XP_006713073.1:p.Asn986= XP_006713073.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X9 XP_016861314.1:p.Asn986= XP_016861314.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X18 XP_016861315.1:p.Asn986= XP_016861315.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X22 XP_016861316.1:p.Asn715= XP_016861316.1:p.Asn715Thr
dedicator of cytokinesis protein 3 isoform X25 XP_011531745.1:p.Asn90= XP_011531745.1:p.Asn90Thr
dedicator of cytokinesis protein 3 isoform X26 XP_011531747.1:p.Asn32= XP_011531747.1:p.Asn32Thr
dedicator of cytokinesis protein 3 isoform X25 XP_011531746.1:p.Asn90= XP_011531746.1:p.Asn90Thr
dedicator of cytokinesis protein 3 isoform X6 XP_047303551.1:p.Asn972= XP_047303551.1:p.Asn972Thr
dedicator of cytokinesis protein 3 isoform X7 XP_047303552.1:p.Asn972= XP_047303552.1:p.Asn972Thr
dedicator of cytokinesis protein 3 isoform X11 XP_047303553.1:p.Asn986= XP_047303553.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X12 XP_047303554.1:p.Asn986= XP_047303554.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X13 XP_047303555.1:p.Asn937= XP_047303555.1:p.Asn937Thr
dedicator of cytokinesis protein 3 isoform X14 XP_047303556.1:p.Asn986= XP_047303556.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X16 XP_047303558.1:p.Asn986= XP_047303558.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X15 XP_047303557.1:p.Asn972= XP_047303557.1:p.Asn972Thr
dedicator of cytokinesis protein 3 isoform X17 XP_047303559.1:p.Asn986= XP_047303559.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X21 XP_047303561.1:p.Asn868= XP_047303561.1:p.Asn868Thr
dedicator of cytokinesis protein 3 isoform X20 XP_047303560.1:p.Asn986= XP_047303560.1:p.Asn986Thr
dedicator of cytokinesis protein 3 isoform X24 XP_047303562.1:p.Asn599= XP_047303562.1:p.Asn599Thr
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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 ss4070845758 Apr 27, 2021 (155)
2 TOPMED ss4564173567 Apr 27, 2021 (155)
3 gnomAD - Genomes NC_000003.12 - 51310266 Apr 27, 2021 (155)
4 TopMed NC_000003.12 - 51310266 Apr 27, 2021 (155)
5 ALFA NC_000003.12 - 51310266 Apr 27, 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
107386043, 401551122, 4004181652, ss4070845758, ss4564173567 NC_000003.12:51310265:A:C NC_000003.12:51310265:A:C (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1488735423

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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