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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.

rs1489153866

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:89632980 (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
G>A / G>C
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.00000 (0/14050, ALFA)
C=0.00000 (0/14050, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LYRM2 : Non Coding Transcript Variant
ANKRD6 : 3 Prime UTR 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 G=1.00000 A=0.00000, C=0.00000 1.0 0.0 0.0 N/A
European Sub 9690 G=1.0000 A=0.0000, C=0.0000 1.0 0.0 0.0 N/A
African Sub 2898 G=1.0000 A=0.0000, C=0.0000 1.0 0.0 0.0 N/A
African Others Sub 114 G=1.000 A=0.000, C=0.000 1.0 0.0 0.0 N/A
African American Sub 2784 G=1.0000 A=0.0000, C=0.0000 1.0 0.0 0.0 N/A
Asian Sub 112 G=1.000 A=0.000, C=0.000 1.0 0.0 0.0 N/A
East Asian Sub 86 G=1.00 A=0.00, C=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 26 G=1.00 A=0.00, C=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 G=1.000 A=0.000, C=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 G=1.000 A=0.000, C=0.000 1.0 0.0 0.0 N/A
South Asian Sub 98 G=1.00 A=0.00, C=0.00 1.0 0.0 0.0 N/A
Other Sub 496 G=1.000 A=0.000, 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
Allele Frequency Aggregator Total Global 14050 G=1.00000 A=0.00000, C=0.00000
Allele Frequency Aggregator European Sub 9690 G=1.0000 A=0.0000, C=0.0000
Allele Frequency Aggregator African Sub 2898 G=1.0000 A=0.0000, C=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 G=1.000 A=0.000, C=0.000
Allele Frequency Aggregator Other Sub 496 G=1.000 A=0.000, C=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 G=1.000 A=0.000, C=0.000
Allele Frequency Aggregator Asian Sub 112 G=1.000 A=0.000, C=0.000
Allele Frequency Aggregator South Asian Sub 98 G=1.00 A=0.00, 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 6 NC_000006.12:g.89632980G>A
GRCh38.p14 chr 6 NC_000006.12:g.89632980G>C
GRCh37.p13 chr 6 NC_000006.11:g.90342699G>A
GRCh37.p13 chr 6 NC_000006.11:g.90342699G>C
Gene: ANKRD6, ankyrin repeat domain 6 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ANKRD6 transcript variant 2 NM_001242811.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant 3 NM_014942.4:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant 4 NM_001242813.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant 5 NM_001242814.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant 1 NM_001242809.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X1 XM_005248679.4:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X2 XM_047418397.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X40 XM_005248681.3:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X3 XM_005248682.4:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X4 XM_024446357.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X41 XM_047418398.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X5 XM_011535596.3:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X6 XM_011535597.3:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X7 XM_017010493.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X8 XM_017010494.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X9 XM_047418399.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X10 XM_047418400.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X11 XM_024446358.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X12 XM_017010496.3:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X42 XM_047418401.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X43 XM_047418402.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X13 XM_024446359.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X14 XM_024446360.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X15 XM_024446361.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X16 XM_005248683.4:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X17 XM_017010499.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X18 XM_017010500.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X19 XM_047418404.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X20 XM_024446362.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X44 XM_047418405.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X21 XM_017010502.3:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X22 XM_017010503.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X23 XM_024446363.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X24 XM_024446364.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X25 XM_024446365.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X26 XM_047418406.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X27 XM_047418407.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X28 XM_017010508.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X29 XM_024446366.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X30 XM_017010511.3:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X31 XM_005248684.4:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X32 XM_024446368.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X45 XM_017010513.2:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X33 XM_047418408.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X46 XM_047418409.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X34 XM_047418410.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X35 XM_047418411.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X36 XM_047418412.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X37 XM_047418413.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X38 XM_047418414.1:c.*1976= N/A 3 Prime UTR Variant
ANKRD6 transcript variant X39 XM_047418415.1:c.*1976= N/A 3 Prime UTR Variant
Gene: LYRM2, LYR motif containing 2 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
LYRM2 transcript variant 1 NM_020466.5:c.*4293= N/A 3 Prime UTR Variant
LYRM2 transcript variant 2 NR_028493.2:n.4746C>T N/A Non Coding Transcript Variant
LYRM2 transcript variant 2 NR_028493.2:n.4746C>G N/A Non Coding Transcript Variant
LYRM2 transcript variant 4 NR_028495.2:n.4597C>T N/A Non Coding Transcript Variant
LYRM2 transcript variant 4 NR_028495.2:n.4597C>G N/A Non Coding Transcript Variant
LYRM2 transcript variant 3 NR_028494.2:n.4729C>T N/A Non Coding Transcript Variant
LYRM2 transcript variant 3 NR_028494.2:n.4729C>G 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 G= A C
GRCh38.p14 chr 6 NC_000006.12:g.89632980= NC_000006.12:g.89632980G>A NC_000006.12:g.89632980G>C
GRCh37.p13 chr 6 NC_000006.11:g.90342699= NC_000006.11:g.90342699G>A NC_000006.11:g.90342699G>C
LYRM2 transcript variant 1 NM_020466.5:c.*4293= NM_020466.5:c.*4293C>T NM_020466.5:c.*4293C>G
LYRM2 transcript variant 1 NM_020466.4:c.*4293= NM_020466.4:c.*4293C>T NM_020466.4:c.*4293C>G
ANKRD6 transcript variant 3 NM_014942.4:c.*1976= NM_014942.4:c.*1976G>A NM_014942.4:c.*1976G>C
ANKRD6 transcript variant X1 XM_005248679.4:c.*1976= XM_005248679.4:c.*1976G>A XM_005248679.4:c.*1976G>C
ANKRD6 transcript variant X1 XM_005248679.3:c.*1976= XM_005248679.3:c.*1976G>A XM_005248679.3:c.*1976G>C
ANKRD6 transcript variant X3 XM_005248682.4:c.*1976= XM_005248682.4:c.*1976G>A XM_005248682.4:c.*1976G>C
ANKRD6 transcript variant X4 XM_005248682.3:c.*1976= XM_005248682.3:c.*1976G>A XM_005248682.3:c.*1976G>C
ANKRD6 transcript variant X16 XM_005248683.4:c.*1976= XM_005248683.4:c.*1976G>A XM_005248683.4:c.*1976G>C
ANKRD6 transcript variant X19 XM_005248683.3:c.*1976= XM_005248683.3:c.*1976G>A XM_005248683.3:c.*1976G>C
ANKRD6 transcript variant X31 XM_005248684.4:c.*1976= XM_005248684.4:c.*1976G>A XM_005248684.4:c.*1976G>C
ANKRD6 transcript variant X35 XM_005248684.3:c.*1976= XM_005248684.3:c.*1976G>A XM_005248684.3:c.*1976G>C
ANKRD6 transcript variant X12 XM_017010496.3:c.*1976= XM_017010496.3:c.*1976G>A XM_017010496.3:c.*1976G>C
ANKRD6 transcript variant X13 XM_017010496.2:c.*1976= XM_017010496.2:c.*1976G>A XM_017010496.2:c.*1976G>C
ANKRD6 transcript variant X11 XM_017010496.1:c.*1976= XM_017010496.1:c.*1976G>A XM_017010496.1:c.*1976G>C
ANKRD6 transcript variant X21 XM_017010502.3:c.*1976= XM_017010502.3:c.*1976G>A XM_017010502.3:c.*1976G>C
ANKRD6 transcript variant X25 XM_017010502.2:c.*1976= XM_017010502.2:c.*1976G>A XM_017010502.2:c.*1976G>C
ANKRD6 transcript variant X20 XM_017010502.1:c.*1976= XM_017010502.1:c.*1976G>A XM_017010502.1:c.*1976G>C
ANKRD6 transcript variant X40 XM_005248681.3:c.*1976= XM_005248681.3:c.*1976G>A XM_005248681.3:c.*1976G>C
ANKRD6 transcript variant X3 XM_005248681.2:c.*1976= XM_005248681.2:c.*1976G>A XM_005248681.2:c.*1976G>C
ANKRD6 transcript variant X30 XM_017010511.3:c.*1976= XM_017010511.3:c.*1976G>A XM_017010511.3:c.*1976G>C
ANKRD6 transcript variant X34 XM_017010511.2:c.*1976= XM_017010511.2:c.*1976G>A XM_017010511.2:c.*1976G>C
ANKRD6 transcript variant X29 XM_017010511.1:c.*1976= XM_017010511.1:c.*1976G>A XM_017010511.1:c.*1976G>C
ANKRD6 transcript variant X6 XM_011535597.3:c.*1976= XM_011535597.3:c.*1976G>A XM_011535597.3:c.*1976G>C
ANKRD6 transcript variant X7 XM_011535597.2:c.*1976= XM_011535597.2:c.*1976G>A XM_011535597.2:c.*1976G>C
ANKRD6 transcript variant X5 XM_011535596.3:c.*1976= XM_011535596.3:c.*1976G>A XM_011535596.3:c.*1976G>C
ANKRD6 transcript variant X6 XM_011535596.2:c.*1976= XM_011535596.2:c.*1976G>A XM_011535596.2:c.*1976G>C
ANKRD6 transcript variant X4 XM_024446357.2:c.*1976= XM_024446357.2:c.*1976G>A XM_024446357.2:c.*1976G>C
ANKRD6 transcript variant X5 XM_024446357.1:c.*1976= XM_024446357.1:c.*1976G>A XM_024446357.1:c.*1976G>C
ANKRD6 transcript variant X11 XM_024446358.2:c.*1976= XM_024446358.2:c.*1976G>A XM_024446358.2:c.*1976G>C
ANKRD6 transcript variant X10 XM_024446358.1:c.*1976= XM_024446358.1:c.*1976G>A XM_024446358.1:c.*1976G>C
ANKRD6 transcript variant X13 XM_024446359.2:c.*1976= XM_024446359.2:c.*1976G>A XM_024446359.2:c.*1976G>C
ANKRD6 transcript variant X15 XM_024446359.1:c.*1976= XM_024446359.1:c.*1976G>A XM_024446359.1:c.*1976G>C
ANKRD6 transcript variant X14 XM_024446360.2:c.*1976= XM_024446360.2:c.*1976G>A XM_024446360.2:c.*1976G>C
ANKRD6 transcript variant X16 XM_024446360.1:c.*1976= XM_024446360.1:c.*1976G>A XM_024446360.1:c.*1976G>C
ANKRD6 transcript variant X15 XM_024446361.2:c.*1976= XM_024446361.2:c.*1976G>A XM_024446361.2:c.*1976G>C
ANKRD6 transcript variant X17 XM_024446361.1:c.*1976= XM_024446361.1:c.*1976G>A XM_024446361.1:c.*1976G>C
ANKRD6 transcript variant X20 XM_024446362.2:c.*1976= XM_024446362.2:c.*1976G>A XM_024446362.2:c.*1976G>C
ANKRD6 transcript variant X23 XM_024446362.1:c.*1976= XM_024446362.1:c.*1976G>A XM_024446362.1:c.*1976G>C
ANKRD6 transcript variant X22 XM_017010503.2:c.*1976= XM_017010503.2:c.*1976G>A XM_017010503.2:c.*1976G>C
ANKRD6 transcript variant X26 XM_017010503.1:c.*1976= XM_017010503.1:c.*1976G>A XM_017010503.1:c.*1976G>C
ANKRD6 transcript variant X23 XM_024446363.2:c.*1976= XM_024446363.2:c.*1976G>A XM_024446363.2:c.*1976G>C
ANKRD6 transcript variant X27 XM_024446363.1:c.*1976= XM_024446363.1:c.*1976G>A XM_024446363.1:c.*1976G>C
ANKRD6 transcript variant X25 XM_024446365.2:c.*1976= XM_024446365.2:c.*1976G>A XM_024446365.2:c.*1976G>C
ANKRD6 transcript variant X30 XM_024446365.1:c.*1976= XM_024446365.1:c.*1976G>A XM_024446365.1:c.*1976G>C
ANKRD6 transcript variant X24 XM_024446364.2:c.*1976= XM_024446364.2:c.*1976G>A XM_024446364.2:c.*1976G>C
ANKRD6 transcript variant X29 XM_024446364.1:c.*1976= XM_024446364.1:c.*1976G>A XM_024446364.1:c.*1976G>C
LYRM2 transcript variant 2 NR_028493.2:n.4746= NR_028493.2:n.4746C>T NR_028493.2:n.4746C>G
LYRM2 transcript variant 2 NR_028493.1:n.4758= NR_028493.1:n.4758C>T NR_028493.1:n.4758C>G
LYRM2 transcript variant 3 NR_028494.2:n.4729= NR_028494.2:n.4729C>T NR_028494.2:n.4729C>G
LYRM2 transcript variant 3 NR_028494.1:n.4741= NR_028494.1:n.4741C>T NR_028494.1:n.4741C>G
ANKRD6 transcript variant X28 XM_017010508.2:c.*1976= XM_017010508.2:c.*1976G>A XM_017010508.2:c.*1976G>C
ANKRD6 transcript variant X31 XM_017010508.1:c.*1976= XM_017010508.1:c.*1976G>A XM_017010508.1:c.*1976G>C
ANKRD6 transcript variant X29 XM_024446366.2:c.*1976= XM_024446366.2:c.*1976G>A XM_024446366.2:c.*1976G>C
ANKRD6 transcript variant X32 XM_024446366.1:c.*1976= XM_024446366.1:c.*1976G>A XM_024446366.1:c.*1976G>C
ANKRD6 transcript variant 1 NM_001242809.2:c.*1976= NM_001242809.2:c.*1976G>A NM_001242809.2:c.*1976G>C
ANKRD6 transcript variant 1 NM_001242809.1:c.*1976= NM_001242809.1:c.*1976G>A NM_001242809.1:c.*1976G>C
LYRM2 transcript variant 4 NR_028495.2:n.4597= NR_028495.2:n.4597C>T NR_028495.2:n.4597C>G
LYRM2 transcript variant 4 NR_028495.1:n.4609= NR_028495.1:n.4609C>T NR_028495.1:n.4609C>G
ANKRD6 transcript variant X32 XM_024446368.2:c.*1976= XM_024446368.2:c.*1976G>A XM_024446368.2:c.*1976G>C
ANKRD6 transcript variant X37 XM_024446368.1:c.*1976= XM_024446368.1:c.*1976G>A XM_024446368.1:c.*1976G>C
ANKRD6 transcript variant X7 XM_017010493.2:c.*1976= XM_017010493.2:c.*1976G>A XM_017010493.2:c.*1976G>C
ANKRD6 transcript variant X8 XM_017010493.1:c.*1976= XM_017010493.1:c.*1976G>A XM_017010493.1:c.*1976G>C
ANKRD6 transcript variant X8 XM_017010494.2:c.*1976= XM_017010494.2:c.*1976G>A XM_017010494.2:c.*1976G>C
ANKRD6 transcript variant X9 XM_017010494.1:c.*1976= XM_017010494.1:c.*1976G>A XM_017010494.1:c.*1976G>C
ANKRD6 transcript variant X17 XM_017010499.2:c.*1976= XM_017010499.2:c.*1976G>A XM_017010499.2:c.*1976G>C
ANKRD6 transcript variant X20 XM_017010499.1:c.*1976= XM_017010499.1:c.*1976G>A XM_017010499.1:c.*1976G>C
ANKRD6 transcript variant X18 XM_017010500.2:c.*1976= XM_017010500.2:c.*1976G>A XM_017010500.2:c.*1976G>C
ANKRD6 transcript variant X21 XM_017010500.1:c.*1976= XM_017010500.1:c.*1976G>A XM_017010500.1:c.*1976G>C
ANKRD6 transcript variant X45 XM_017010513.2:c.*1976= XM_017010513.2:c.*1976G>A XM_017010513.2:c.*1976G>C
ANKRD6 transcript variant X38 XM_017010513.1:c.*1976= XM_017010513.1:c.*1976G>A XM_017010513.1:c.*1976G>C
ANKRD6 transcript variant 2 NM_001242811.1:c.*1976= NM_001242811.1:c.*1976G>A NM_001242811.1:c.*1976G>C
ANKRD6 transcript variant X9 XM_047418399.1:c.*1976= XM_047418399.1:c.*1976G>A XM_047418399.1:c.*1976G>C
ANKRD6 transcript variant X10 XM_047418400.1:c.*1976= XM_047418400.1:c.*1976G>A XM_047418400.1:c.*1976G>C
ANKRD6 transcript variant X19 XM_047418404.1:c.*1976= XM_047418404.1:c.*1976G>A XM_047418404.1:c.*1976G>C
ANKRD6 transcript variant X27 XM_047418407.1:c.*1976= XM_047418407.1:c.*1976G>A XM_047418407.1:c.*1976G>C
ANKRD6 transcript variant X41 XM_047418398.1:c.*1976= XM_047418398.1:c.*1976G>A XM_047418398.1:c.*1976G>C
ANKRD6 transcript variant X43 XM_047418402.1:c.*1976= XM_047418402.1:c.*1976G>A XM_047418402.1:c.*1976G>C
ANKRD6 transcript variant X42 XM_047418401.1:c.*1976= XM_047418401.1:c.*1976G>A XM_047418401.1:c.*1976G>C
ANKRD6 transcript variant 4 NM_001242813.1:c.*1976= NM_001242813.1:c.*1976G>A NM_001242813.1:c.*1976G>C
ANKRD6 transcript variant X44 XM_047418405.1:c.*1976= XM_047418405.1:c.*1976G>A XM_047418405.1:c.*1976G>C
ANKRD6 transcript variant X2 XM_047418397.1:c.*1976= XM_047418397.1:c.*1976G>A XM_047418397.1:c.*1976G>C
ANKRD6 transcript variant X35 XM_047418411.1:c.*1976= XM_047418411.1:c.*1976G>A XM_047418411.1:c.*1976G>C
ANKRD6 transcript variant X33 XM_047418408.1:c.*1976= XM_047418408.1:c.*1976G>A XM_047418408.1:c.*1976G>C
ANKRD6 transcript variant X34 XM_047418410.1:c.*1976= XM_047418410.1:c.*1976G>A XM_047418410.1:c.*1976G>C
ANKRD6 transcript variant X36 XM_047418412.1:c.*1976= XM_047418412.1:c.*1976G>A XM_047418412.1:c.*1976G>C
ANKRD6 transcript variant 5 NM_001242814.1:c.*1976= NM_001242814.1:c.*1976G>A NM_001242814.1:c.*1976G>C
ANKRD6 transcript variant X46 XM_047418409.1:c.*1976= XM_047418409.1:c.*1976G>A XM_047418409.1:c.*1976G>C
ANKRD6 transcript variant X26 XM_047418406.1:c.*1976= XM_047418406.1:c.*1976G>A XM_047418406.1:c.*1976G>C
ANKRD6 transcript variant X37 XM_047418413.1:c.*1976= XM_047418413.1:c.*1976G>A XM_047418413.1:c.*1976G>C
ANKRD6 transcript variant X39 XM_047418415.1:c.*1976= XM_047418415.1:c.*1976G>A XM_047418415.1:c.*1976G>C
ANKRD6 transcript variant X38 XM_047418414.1:c.*1976= XM_047418414.1:c.*1976G>A XM_047418414.1:c.*1976G>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#.

1 Frequency submission
No Submitter Submission ID Date (Build)
1 ALFA NC_000006.12 - 89632980 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
521166057 NC_000006.12:89632979:G:A NC_000006.12:89632979:G:A (self)
521166057 NC_000006.12:89632979:G:C NC_000006.12:89632979:G: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 rs1489153866

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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