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dbSNP Short Genetic Variations

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.

rs34529047

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:171256273-171256294 (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
del(A)12 / del(A)10 / del(A)9 / de…

del(A)12 / del(A)10 / del(A)9 / del(A)8 / del(A)7 / del(A)6 / del(A)5 / del(A)4 / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)4 / dup(A)5 / dup(A)6

Variation Type
Indel Insertion and Deletion
Frequency
del(A)12=0.0000 (0/1986, ALFA)
del(A)10=0.0000 (0/1986, ALFA)
del(A)9=0.0000 (0/1986, ALFA) (+ 11 more)
del(A)8=0.0000 (0/1986, ALFA)
del(A)7=0.0000 (0/1986, ALFA)
del(A)6=0.0000 (0/1986, ALFA)
del(A)5=0.0000 (0/1986, ALFA)
del(A)4=0.0000 (0/1986, ALFA)
delAAA=0.0000 (0/1986, ALFA)
delAA=0.0000 (0/1986, ALFA)
delA=0.0000 (0/1986, ALFA)
dupA=0.0000 (0/1986, ALFA)
dupAA=0.0000 (0/1986, ALFA)
dup(A)4=0.0000 (0/1986, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
FMO1 : Intron 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 1986 AAAAAAAAAAAAAAAAAAAAAA=1.0000 AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000 1.0 0.0 0.0 N/A
European Sub 1782 AAAAAAAAAAAAAAAAAAAAAA=1.0000 AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000 1.0 0.0 0.0 N/A
African Sub 24 AAAAAAAAAAAAAAAAAAAAAA=1.00 AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00 1.0 0.0 0.0 N/A
African Others Sub 0 AAAAAAAAAAAAAAAAAAAAAA=0 AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0 0 0 0 N/A
African American Sub 24 AAAAAAAAAAAAAAAAAAAAAA=1.00 AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00 1.0 0.0 0.0 N/A
Asian Sub 10 AAAAAAAAAAAAAAAAAAAAAA=1.0 AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0 1.0 0.0 0.0 N/A
East Asian Sub 6 AAAAAAAAAAAAAAAAAAAAAA=1.0 AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0 1.0 0.0 0.0 N/A
Other Asian Sub 4 AAAAAAAAAAAAAAAAAAAAAA=1.0 AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0 1.0 0.0 0.0 N/A
Latin American 1 Sub 14 AAAAAAAAAAAAAAAAAAAAAA=1.00 AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00 1.0 0.0 0.0 N/A
Latin American 2 Sub 64 AAAAAAAAAAAAAAAAAAAAAA=1.00 AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00 1.0 0.0 0.0 N/A
South Asian Sub 12 AAAAAAAAAAAAAAAAAAAAAA=1.00 AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00 1.0 0.0 0.0 N/A
Other Sub 80 AAAAAAAAAAAAAAAAAAAAAA=1.00 AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00 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 1986 (A)22=1.0000 del(A)12=0.0000, del(A)10=0.0000, del(A)9=0.0000, del(A)8=0.0000, del(A)7=0.0000, del(A)6=0.0000, del(A)5=0.0000, del(A)4=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)4=0.0000
Allele Frequency Aggregator European Sub 1782 (A)22=1.0000 del(A)12=0.0000, del(A)10=0.0000, del(A)9=0.0000, del(A)8=0.0000, del(A)7=0.0000, del(A)6=0.0000, del(A)5=0.0000, del(A)4=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)4=0.0000
Allele Frequency Aggregator Other Sub 80 (A)22=1.00 del(A)12=0.00, del(A)10=0.00, del(A)9=0.00, del(A)8=0.00, del(A)7=0.00, del(A)6=0.00, del(A)5=0.00, del(A)4=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)4=0.00
Allele Frequency Aggregator Latin American 2 Sub 64 (A)22=1.00 del(A)12=0.00, del(A)10=0.00, del(A)9=0.00, del(A)8=0.00, del(A)7=0.00, del(A)6=0.00, del(A)5=0.00, del(A)4=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)4=0.00
Allele Frequency Aggregator African Sub 24 (A)22=1.00 del(A)12=0.00, del(A)10=0.00, del(A)9=0.00, del(A)8=0.00, del(A)7=0.00, del(A)6=0.00, del(A)5=0.00, del(A)4=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)4=0.00
Allele Frequency Aggregator Latin American 1 Sub 14 (A)22=1.00 del(A)12=0.00, del(A)10=0.00, del(A)9=0.00, del(A)8=0.00, del(A)7=0.00, del(A)6=0.00, del(A)5=0.00, del(A)4=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)4=0.00
Allele Frequency Aggregator South Asian Sub 12 (A)22=1.00 del(A)12=0.00, del(A)10=0.00, del(A)9=0.00, del(A)8=0.00, del(A)7=0.00, del(A)6=0.00, del(A)5=0.00, del(A)4=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)4=0.00
Allele Frequency Aggregator Asian Sub 10 (A)22=1.0 del(A)12=0.0, del(A)10=0.0, del(A)9=0.0, del(A)8=0.0, del(A)7=0.0, del(A)6=0.0, del(A)5=0.0, del(A)4=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dup(A)4=0.0
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 1 NC_000001.11:g.171256283_171256294del
GRCh38.p14 chr 1 NC_000001.11:g.171256285_171256294del
GRCh38.p14 chr 1 NC_000001.11:g.171256286_171256294del
GRCh38.p14 chr 1 NC_000001.11:g.171256287_171256294del
GRCh38.p14 chr 1 NC_000001.11:g.171256288_171256294del
GRCh38.p14 chr 1 NC_000001.11:g.171256289_171256294del
GRCh38.p14 chr 1 NC_000001.11:g.171256290_171256294del
GRCh38.p14 chr 1 NC_000001.11:g.171256291_171256294del
GRCh38.p14 chr 1 NC_000001.11:g.171256292_171256294del
GRCh38.p14 chr 1 NC_000001.11:g.171256293_171256294del
GRCh38.p14 chr 1 NC_000001.11:g.171256294del
GRCh38.p14 chr 1 NC_000001.11:g.171256294dup
GRCh38.p14 chr 1 NC_000001.11:g.171256293_171256294dup
GRCh38.p14 chr 1 NC_000001.11:g.171256292_171256294dup
GRCh38.p14 chr 1 NC_000001.11:g.171256291_171256294dup
GRCh38.p14 chr 1 NC_000001.11:g.171256290_171256294dup
GRCh38.p14 chr 1 NC_000001.11:g.171256289_171256294dup
GRCh37.p13 chr 1 NC_000001.10:g.171225422_171225433del
GRCh37.p13 chr 1 NC_000001.10:g.171225424_171225433del
GRCh37.p13 chr 1 NC_000001.10:g.171225425_171225433del
GRCh37.p13 chr 1 NC_000001.10:g.171225426_171225433del
GRCh37.p13 chr 1 NC_000001.10:g.171225427_171225433del
GRCh37.p13 chr 1 NC_000001.10:g.171225428_171225433del
GRCh37.p13 chr 1 NC_000001.10:g.171225429_171225433del
GRCh37.p13 chr 1 NC_000001.10:g.171225430_171225433del
GRCh37.p13 chr 1 NC_000001.10:g.171225431_171225433del
GRCh37.p13 chr 1 NC_000001.10:g.171225432_171225433del
GRCh37.p13 chr 1 NC_000001.10:g.171225433del
GRCh37.p13 chr 1 NC_000001.10:g.171225433dup
GRCh37.p13 chr 1 NC_000001.10:g.171225432_171225433dup
GRCh37.p13 chr 1 NC_000001.10:g.171225431_171225433dup
GRCh37.p13 chr 1 NC_000001.10:g.171225430_171225433dup
GRCh37.p13 chr 1 NC_000001.10:g.171225429_171225433dup
GRCh37.p13 chr 1 NC_000001.10:g.171225428_171225433dup
Gene: FMO1, flavin containing dimethylaniline monoxygenase 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
FMO1 transcript variant 3 NM_001282693.2:c.-6-1799_…

NM_001282693.2:c.-6-1799_-6-1788del

N/A Intron Variant
FMO1 transcript variant 4 NM_001282694.2:c.-6-1799_…

NM_001282694.2:c.-6-1799_-6-1788del

N/A Intron Variant
FMO1 transcript variant 2 NM_002021.3:c.-6-1799_-6-…

NM_002021.3:c.-6-1799_-6-1788del

N/A Intron Variant
FMO1 transcript variant 1 NM_001282692.1:c. N/A Genic Upstream Transcript Variant
FMO1 transcript variant X4 XM_005245038.5:c.-6-1799_…

XM_005245038.5:c.-6-1799_-6-1788del

N/A Intron Variant
FMO1 transcript variant X1 XM_006711241.5:c.-6-1799_…

XM_006711241.5:c.-6-1799_-6-1788del

N/A Intron Variant
FMO1 transcript variant X3 XM_006711242.5:c.-6-1799_…

XM_006711242.5:c.-6-1799_-6-1788del

N/A Intron Variant
FMO1 transcript variant X2 XM_005245037.4:c. N/A Genic Upstream 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)22= del(A)12 del(A)10 del(A)9 del(A)8 del(A)7 del(A)6 del(A)5 del(A)4 delAAA delAA delA dupA dupAA dupAAA dup(A)4 dup(A)5 dup(A)6
GRCh38.p14 chr 1 NC_000001.11:g.171256273_171256294= NC_000001.11:g.171256283_171256294del NC_000001.11:g.171256285_171256294del NC_000001.11:g.171256286_171256294del NC_000001.11:g.171256287_171256294del NC_000001.11:g.171256288_171256294del NC_000001.11:g.171256289_171256294del NC_000001.11:g.171256290_171256294del NC_000001.11:g.171256291_171256294del NC_000001.11:g.171256292_171256294del NC_000001.11:g.171256293_171256294del NC_000001.11:g.171256294del NC_000001.11:g.171256294dup NC_000001.11:g.171256293_171256294dup NC_000001.11:g.171256292_171256294dup NC_000001.11:g.171256291_171256294dup NC_000001.11:g.171256290_171256294dup NC_000001.11:g.171256289_171256294dup
GRCh37.p13 chr 1 NC_000001.10:g.171225412_171225433= NC_000001.10:g.171225422_171225433del NC_000001.10:g.171225424_171225433del NC_000001.10:g.171225425_171225433del NC_000001.10:g.171225426_171225433del NC_000001.10:g.171225427_171225433del NC_000001.10:g.171225428_171225433del NC_000001.10:g.171225429_171225433del NC_000001.10:g.171225430_171225433del NC_000001.10:g.171225431_171225433del NC_000001.10:g.171225432_171225433del NC_000001.10:g.171225433del NC_000001.10:g.171225433dup NC_000001.10:g.171225432_171225433dup NC_000001.10:g.171225431_171225433dup NC_000001.10:g.171225430_171225433dup NC_000001.10:g.171225429_171225433dup NC_000001.10:g.171225428_171225433dup
FMO1 transcript variant 3 NM_001282693.2:c.-6-1809= NM_001282693.2:c.-6-1799_-6-1788del NM_001282693.2:c.-6-1797_-6-1788del NM_001282693.2:c.-6-1796_-6-1788del NM_001282693.2:c.-6-1795_-6-1788del NM_001282693.2:c.-6-1794_-6-1788del NM_001282693.2:c.-6-1793_-6-1788del NM_001282693.2:c.-6-1792_-6-1788del NM_001282693.2:c.-6-1791_-6-1788del NM_001282693.2:c.-6-1790_-6-1788del NM_001282693.2:c.-6-1789_-6-1788del NM_001282693.2:c.-6-1788del NM_001282693.2:c.-6-1788dup NM_001282693.2:c.-6-1789_-6-1788dup NM_001282693.2:c.-6-1790_-6-1788dup NM_001282693.2:c.-6-1791_-6-1788dup NM_001282693.2:c.-6-1792_-6-1788dup NM_001282693.2:c.-6-1793_-6-1788dup
FMO1 transcript variant 4 NM_001282694.2:c.-6-1809= NM_001282694.2:c.-6-1799_-6-1788del NM_001282694.2:c.-6-1797_-6-1788del NM_001282694.2:c.-6-1796_-6-1788del NM_001282694.2:c.-6-1795_-6-1788del NM_001282694.2:c.-6-1794_-6-1788del NM_001282694.2:c.-6-1793_-6-1788del NM_001282694.2:c.-6-1792_-6-1788del NM_001282694.2:c.-6-1791_-6-1788del NM_001282694.2:c.-6-1790_-6-1788del NM_001282694.2:c.-6-1789_-6-1788del NM_001282694.2:c.-6-1788del NM_001282694.2:c.-6-1788dup NM_001282694.2:c.-6-1789_-6-1788dup NM_001282694.2:c.-6-1790_-6-1788dup NM_001282694.2:c.-6-1791_-6-1788dup NM_001282694.2:c.-6-1792_-6-1788dup NM_001282694.2:c.-6-1793_-6-1788dup
FMO1 transcript NM_002021.1:c.-6-1809= NM_002021.1:c.-6-1799_-6-1788del NM_002021.1:c.-6-1797_-6-1788del NM_002021.1:c.-6-1796_-6-1788del NM_002021.1:c.-6-1795_-6-1788del NM_002021.1:c.-6-1794_-6-1788del NM_002021.1:c.-6-1793_-6-1788del NM_002021.1:c.-6-1792_-6-1788del NM_002021.1:c.-6-1791_-6-1788del NM_002021.1:c.-6-1790_-6-1788del NM_002021.1:c.-6-1789_-6-1788del NM_002021.1:c.-6-1788del NM_002021.1:c.-6-1788dup NM_002021.1:c.-6-1789_-6-1788dup NM_002021.1:c.-6-1790_-6-1788dup NM_002021.1:c.-6-1791_-6-1788dup NM_002021.1:c.-6-1792_-6-1788dup NM_002021.1:c.-6-1793_-6-1788dup
FMO1 transcript variant 2 NM_002021.3:c.-6-1809= NM_002021.3:c.-6-1799_-6-1788del NM_002021.3:c.-6-1797_-6-1788del NM_002021.3:c.-6-1796_-6-1788del NM_002021.3:c.-6-1795_-6-1788del NM_002021.3:c.-6-1794_-6-1788del NM_002021.3:c.-6-1793_-6-1788del NM_002021.3:c.-6-1792_-6-1788del NM_002021.3:c.-6-1791_-6-1788del NM_002021.3:c.-6-1790_-6-1788del NM_002021.3:c.-6-1789_-6-1788del NM_002021.3:c.-6-1788del NM_002021.3:c.-6-1788dup NM_002021.3:c.-6-1789_-6-1788dup NM_002021.3:c.-6-1790_-6-1788dup NM_002021.3:c.-6-1791_-6-1788dup NM_002021.3:c.-6-1792_-6-1788dup NM_002021.3:c.-6-1793_-6-1788dup
FMO1 transcript variant X1 XM_005245034.1:c.-6-1809= XM_005245034.1:c.-6-1799_-6-1788del XM_005245034.1:c.-6-1797_-6-1788del XM_005245034.1:c.-6-1796_-6-1788del XM_005245034.1:c.-6-1795_-6-1788del XM_005245034.1:c.-6-1794_-6-1788del XM_005245034.1:c.-6-1793_-6-1788del XM_005245034.1:c.-6-1792_-6-1788del XM_005245034.1:c.-6-1791_-6-1788del XM_005245034.1:c.-6-1790_-6-1788del XM_005245034.1:c.-6-1789_-6-1788del XM_005245034.1:c.-6-1788del XM_005245034.1:c.-6-1788dup XM_005245034.1:c.-6-1789_-6-1788dup XM_005245034.1:c.-6-1790_-6-1788dup XM_005245034.1:c.-6-1791_-6-1788dup XM_005245034.1:c.-6-1792_-6-1788dup XM_005245034.1:c.-6-1793_-6-1788dup
FMO1 transcript variant X2 XM_005245035.1:c.-6-1809= XM_005245035.1:c.-6-1799_-6-1788del XM_005245035.1:c.-6-1797_-6-1788del XM_005245035.1:c.-6-1796_-6-1788del XM_005245035.1:c.-6-1795_-6-1788del XM_005245035.1:c.-6-1794_-6-1788del XM_005245035.1:c.-6-1793_-6-1788del XM_005245035.1:c.-6-1792_-6-1788del XM_005245035.1:c.-6-1791_-6-1788del XM_005245035.1:c.-6-1790_-6-1788del XM_005245035.1:c.-6-1789_-6-1788del XM_005245035.1:c.-6-1788del XM_005245035.1:c.-6-1788dup XM_005245035.1:c.-6-1789_-6-1788dup XM_005245035.1:c.-6-1790_-6-1788dup XM_005245035.1:c.-6-1791_-6-1788dup XM_005245035.1:c.-6-1792_-6-1788dup XM_005245035.1:c.-6-1793_-6-1788dup
FMO1 transcript variant X5 XM_005245038.1:c.-6-1809= XM_005245038.1:c.-6-1799_-6-1788del XM_005245038.1:c.-6-1797_-6-1788del XM_005245038.1:c.-6-1796_-6-1788del XM_005245038.1:c.-6-1795_-6-1788del XM_005245038.1:c.-6-1794_-6-1788del XM_005245038.1:c.-6-1793_-6-1788del XM_005245038.1:c.-6-1792_-6-1788del XM_005245038.1:c.-6-1791_-6-1788del XM_005245038.1:c.-6-1790_-6-1788del XM_005245038.1:c.-6-1789_-6-1788del XM_005245038.1:c.-6-1788del XM_005245038.1:c.-6-1788dup XM_005245038.1:c.-6-1789_-6-1788dup XM_005245038.1:c.-6-1790_-6-1788dup XM_005245038.1:c.-6-1791_-6-1788dup XM_005245038.1:c.-6-1792_-6-1788dup XM_005245038.1:c.-6-1793_-6-1788dup
FMO1 transcript variant X4 XM_005245038.5:c.-6-1809= XM_005245038.5:c.-6-1799_-6-1788del XM_005245038.5:c.-6-1797_-6-1788del XM_005245038.5:c.-6-1796_-6-1788del XM_005245038.5:c.-6-1795_-6-1788del XM_005245038.5:c.-6-1794_-6-1788del XM_005245038.5:c.-6-1793_-6-1788del XM_005245038.5:c.-6-1792_-6-1788del XM_005245038.5:c.-6-1791_-6-1788del XM_005245038.5:c.-6-1790_-6-1788del XM_005245038.5:c.-6-1789_-6-1788del XM_005245038.5:c.-6-1788del XM_005245038.5:c.-6-1788dup XM_005245038.5:c.-6-1789_-6-1788dup XM_005245038.5:c.-6-1790_-6-1788dup XM_005245038.5:c.-6-1791_-6-1788dup XM_005245038.5:c.-6-1792_-6-1788dup XM_005245038.5:c.-6-1793_-6-1788dup
FMO1 transcript variant X1 XM_006711241.5:c.-6-1809= XM_006711241.5:c.-6-1799_-6-1788del XM_006711241.5:c.-6-1797_-6-1788del XM_006711241.5:c.-6-1796_-6-1788del XM_006711241.5:c.-6-1795_-6-1788del XM_006711241.5:c.-6-1794_-6-1788del XM_006711241.5:c.-6-1793_-6-1788del XM_006711241.5:c.-6-1792_-6-1788del XM_006711241.5:c.-6-1791_-6-1788del XM_006711241.5:c.-6-1790_-6-1788del XM_006711241.5:c.-6-1789_-6-1788del XM_006711241.5:c.-6-1788del XM_006711241.5:c.-6-1788dup XM_006711241.5:c.-6-1789_-6-1788dup XM_006711241.5:c.-6-1790_-6-1788dup XM_006711241.5:c.-6-1791_-6-1788dup XM_006711241.5:c.-6-1792_-6-1788dup XM_006711241.5:c.-6-1793_-6-1788dup
FMO1 transcript variant X3 XM_006711242.5:c.-6-1809= XM_006711242.5:c.-6-1799_-6-1788del XM_006711242.5:c.-6-1797_-6-1788del XM_006711242.5:c.-6-1796_-6-1788del XM_006711242.5:c.-6-1795_-6-1788del XM_006711242.5:c.-6-1794_-6-1788del XM_006711242.5:c.-6-1793_-6-1788del XM_006711242.5:c.-6-1792_-6-1788del XM_006711242.5:c.-6-1791_-6-1788del XM_006711242.5:c.-6-1790_-6-1788del XM_006711242.5:c.-6-1789_-6-1788del XM_006711242.5:c.-6-1788del XM_006711242.5:c.-6-1788dup XM_006711242.5:c.-6-1789_-6-1788dup XM_006711242.5:c.-6-1790_-6-1788dup XM_006711242.5:c.-6-1791_-6-1788dup XM_006711242.5:c.-6-1792_-6-1788dup XM_006711242.5:c.-6-1793_-6-1788dup
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#.

40 SubSNP, 22 Frequency submissions
No Submitter Submission ID Date (Build)
1 ABI ss41089033 Dec 03, 2013 (138)
2 HGSV ss79978832 Dec 14, 2007 (137)
3 HGSV ss83250248 Aug 21, 2014 (142)
4 SWEGEN ss2987943388 Nov 08, 2017 (151)
5 EVA_DECODE ss3688013156 Jul 12, 2019 (153)
6 EVA_DECODE ss3688013157 Jul 12, 2019 (153)
7 EVA_DECODE ss3688013158 Jul 12, 2019 (153)
8 EVA_DECODE ss3688013159 Jul 12, 2019 (153)
9 EVA_DECODE ss3688013160 Jul 12, 2019 (153)
10 EVA ss3826487637 Apr 25, 2020 (154)
11 GNOMAD ss4005739677 Apr 25, 2021 (155)
12 GNOMAD ss4005739678 Apr 25, 2021 (155)
13 GNOMAD ss4005739679 Apr 25, 2021 (155)
14 GNOMAD ss4005739680 Apr 25, 2021 (155)
15 GNOMAD ss4005739681 Apr 25, 2021 (155)
16 GNOMAD ss4005739682 Apr 25, 2021 (155)
17 GNOMAD ss4005739683 Apr 25, 2021 (155)
18 GNOMAD ss4005739684 Apr 25, 2021 (155)
19 GNOMAD ss4005739685 Apr 25, 2021 (155)
20 GNOMAD ss4005739686 Apr 25, 2021 (155)
21 GNOMAD ss4005739687 Apr 25, 2021 (155)
22 GNOMAD ss4005739688 Apr 25, 2021 (155)
23 GNOMAD ss4005739689 Apr 25, 2021 (155)
24 TOMMO_GENOMICS ss5147010784 Apr 25, 2021 (155)
25 TOMMO_GENOMICS ss5147010785 Apr 25, 2021 (155)
26 TOMMO_GENOMICS ss5147010786 Apr 25, 2021 (155)
27 TOMMO_GENOMICS ss5147010787 Apr 25, 2021 (155)
28 1000G_HIGH_COVERAGE ss5244698973 Oct 12, 2022 (156)
29 1000G_HIGH_COVERAGE ss5244698974 Oct 12, 2022 (156)
30 1000G_HIGH_COVERAGE ss5244698975 Oct 12, 2022 (156)
31 1000G_HIGH_COVERAGE ss5244698977 Oct 12, 2022 (156)
32 HUGCELL_USP ss5445244856 Oct 12, 2022 (156)
33 HUGCELL_USP ss5445244857 Oct 12, 2022 (156)
34 HUGCELL_USP ss5445244858 Oct 12, 2022 (156)
35 TOMMO_GENOMICS ss5674361221 Oct 12, 2022 (156)
36 TOMMO_GENOMICS ss5674361222 Oct 12, 2022 (156)
37 TOMMO_GENOMICS ss5674361223 Oct 12, 2022 (156)
38 TOMMO_GENOMICS ss5674361224 Oct 12, 2022 (156)
39 EVA ss5832828134 Oct 12, 2022 (156)
40 EVA ss5832828135 Oct 12, 2022 (156)
41 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
42 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
43 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
44 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
45 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
46 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
47 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
48 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
49 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
50 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
51 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
52 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
53 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 30406657 (NC_000001.11:171256272::A 1191/71114)
Row 30406658 (NC_000001.11:171256272::AA 119/71036)
Row 30406659 (NC_000001.11:171256272::AAA 24/71246)...

- Apr 25, 2021 (155)
54 8.3KJPN

Submission ignored due to conflicting rows:
Row 4980091 (NC_000001.10:171225411:A: 6498/16478)
Row 4980092 (NC_000001.10:171225411:AA: 2409/16478)
Row 4980093 (NC_000001.10:171225411:AAA: 7/16478)...

- Apr 25, 2021 (155)
55 8.3KJPN

Submission ignored due to conflicting rows:
Row 4980091 (NC_000001.10:171225411:A: 6498/16478)
Row 4980092 (NC_000001.10:171225411:AA: 2409/16478)
Row 4980093 (NC_000001.10:171225411:AAA: 7/16478)...

- Apr 25, 2021 (155)
56 8.3KJPN

Submission ignored due to conflicting rows:
Row 4980091 (NC_000001.10:171225411:A: 6498/16478)
Row 4980092 (NC_000001.10:171225411:AA: 2409/16478)
Row 4980093 (NC_000001.10:171225411:AAA: 7/16478)...

- Apr 25, 2021 (155)
57 8.3KJPN

Submission ignored due to conflicting rows:
Row 4980091 (NC_000001.10:171225411:A: 6498/16478)
Row 4980092 (NC_000001.10:171225411:AA: 2409/16478)
Row 4980093 (NC_000001.10:171225411:AAA: 7/16478)...

- Apr 25, 2021 (155)
58 14KJPN

Submission ignored due to conflicting rows:
Row 8198325 (NC_000001.11:171256272:AA: 4918/28086)
Row 8198326 (NC_000001.11:171256272:A: 12673/28086)
Row 8198327 (NC_000001.11:171256272::A 25/28086)...

- Oct 12, 2022 (156)
59 14KJPN

Submission ignored due to conflicting rows:
Row 8198325 (NC_000001.11:171256272:AA: 4918/28086)
Row 8198326 (NC_000001.11:171256272:A: 12673/28086)
Row 8198327 (NC_000001.11:171256272::A 25/28086)...

- Oct 12, 2022 (156)
60 14KJPN

Submission ignored due to conflicting rows:
Row 8198325 (NC_000001.11:171256272:AA: 4918/28086)
Row 8198326 (NC_000001.11:171256272:A: 12673/28086)
Row 8198327 (NC_000001.11:171256272::A 25/28086)...

- Oct 12, 2022 (156)
61 14KJPN

Submission ignored due to conflicting rows:
Row 8198325 (NC_000001.11:171256272:AA: 4918/28086)
Row 8198326 (NC_000001.11:171256272:A: 12673/28086)
Row 8198327 (NC_000001.11:171256272::A 25/28086)...

- Oct 12, 2022 (156)
62 ALFA NC_000001.11 - 171256273 Apr 25, 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).

Associated ID History Updated (Build)
rs56696804 Apr 25, 2013 (138)
rs57088146 May 11, 2012 (137)
rs71660335 May 11, 2012 (137)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss4005739689 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAA:

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA

(self)
ss4005739688 NC_000001.11:171256272:AAAAAAAAA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA

(self)
ss4005739687 NC_000001.11:171256272:AAAAAAAA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

(self)
ss3688013160 NC_000001.11:171256272:AAAAA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

(self)
ss4005739686 NC_000001.11:171256272:AAAA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

(self)
ss5147010786 NC_000001.10:171225411:AAA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

(self)
ss4005739685, ss5244698977, ss5674361224 NC_000001.11:171256272:AAA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

(self)
ss3688013159 NC_000001.11:171256274:AAA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

(self)
ss83250248 NC_000001.8:167957089:AA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

(self)
ss2987943388, ss5147010785, ss5832828135 NC_000001.10:171225411:AA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

(self)
ss4005739684, ss5244698974, ss5445244858, ss5674361221 NC_000001.11:171256272:AA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

(self)
ss3688013158 NC_000001.11:171256275:AA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

(self)
ss79978832 NC_000001.8:167957090:A: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

(self)
ss5147010784 NC_000001.10:171225411:A: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

(self)
ss4005739683, ss5244698973, ss5445244856, ss5674361222 NC_000001.11:171256272:A: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

(self)
ss3688013157 NC_000001.11:171256276:A: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

(self)
ss41089033 NT_004487.19:22714053:A: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA

(self)
ss3826487637, ss5147010787 NC_000001.10:171225411::A NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

(self)
ss4005739677, ss5244698975, ss5445244857, ss5674361223 NC_000001.11:171256272::A NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

(self)
ss3688013156 NC_000001.11:171256277::A NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

(self)
ss5832828134 NC_000001.10:171225411::AA NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA

ss4005739678 NC_000001.11:171256272::AA NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA

(self)
ss4005739679 NC_000001.11:171256272::AAA NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA

(self)
ss4005739680 NC_000001.11:171256272::AAAA NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA

(self)
2290380145 NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA

NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA

(self)
ss4005739681 NC_000001.11:171256272::AAAAA NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA

(self)
ss4005739682 NC_000001.11:171256272::AAAAAA NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA

(self)
Removed from this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Destination RSIDs
ss3095164829 NC_000001.11:171256272:AAAAAA: NC_000001.11:171256272:AAAAAAAAAAA…

NC_000001.11:171256272:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

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 rs34529047

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