Name: rs1491071832
Published: September 21, 2022
License: Open Access

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.

rs1491071832

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:15627130 (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: dupT / insTT / insTTT / ins(T)₄ / …
dupT / insTT / insTTT / ins(T)₄ / ins(T)₅ / ins(T)₇ / ins(T)₉ / ins(T)₁₁ / ins(T)₁₅ / ins(T)₁₇ / ins(T)₁₈ / ins(T)₂₁ / ins(T)₂₆
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.00008 (1/11862, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FBXL5 : 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	HTRZ	HWEP
Total	Global	11862	T=0.99992	TT=0.00008	0.999831	0.000169	0
European	Sub	7618	T=1.0000	TT=0.0000	1.0	0.0	N/A
African	Sub	2816	T=0.9996	TT=0.0004	0.99929	0.00071	0
African Others	Sub	108	T=1.000	TT=0.000	1.0	0.0	N/A
African American	Sub	2708	T=0.9996	TT=0.0004	0.999261	0.000739	0
Asian	Sub	108	T=1.000	TT=0.000	1.0	0.0	N/A
East Asian	Sub	84	T=1.00	TT=0.00	1.0	0.0	N/A
Other Asian	Sub	24	T=1.00	TT=0.00	1.0	0.0	N/A
Latin American 1	Sub	146	T=1.000	TT=0.000	1.0	0.0	N/A
Latin American 2	Sub	610	T=1.000	TT=0.000	1.0	0.0	N/A
South Asian	Sub	94	T=1.00	TT=0.00	1.0	0.0	N/A
Other	Sub	470	T=1.000	TT=0.000	1.0	0.0	N/A

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11862	T=0.99992	dupT=0.00008
Allele Frequency Aggregator	European	Sub	7618	T=1.0000	dupT=0.0000
Allele Frequency Aggregator	African	Sub	2816	T=0.9996	dupT=0.0004
Allele Frequency Aggregator	Latin American 2	Sub	610	T=1.000	dupT=0.000
Allele Frequency Aggregator	Other	Sub	470	T=1.000	dupT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	T=1.000	dupT=0.000
Allele Frequency Aggregator	Asian	Sub	108	T=1.000	dupT=0.000
Allele Frequency Aggregator	South Asian	Sub	94	T=1.00	dupT=0.00

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 4	NC_000004.12:g.15627130dup
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTT
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTTT
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTTTT
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.15627130_15627131insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753dup
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753_15628754insTTTTTTTTTTTTTTTTTTTTTTTTTT
FBXL5 RefSeqGene	NG_047143.1:g.37788dup
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAA
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAAA
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAAAA
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAAAAA
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAAAAAAA
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAAAAAAAAA
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAAAAAAAAAAA
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAAAAAAAAAAAAAAA
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAAAAAAAAAAAAAAAAA
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAAAAAAAAAAAAAAAAAA
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAAAAAAAAAAAAAAAAAAAAA
FBXL5 RefSeqGene	NG_047143.1:g.37788_37789insAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: FBXL5, F-box and leucine rich repeat protein 5 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FBXL5 transcript variant 3	NM_001193534.2:c.1039-175… NM_001193534.2:c.1039-175dup	N/A	Intron Variant
FBXL5 transcript variant 4	NM_001193535.2:c.991-175d… NM_001193535.2:c.991-175dup	N/A	Intron Variant
FBXL5 transcript variant 1	NM_012161.4:c.1042-175dup	N/A	Intron Variant
FBXL5 transcript variant 2	NR_036464.2:n.	N/A	Intron Variant
FBXL5 transcript variant X5	XM_006713959.4:c.985-175d… XM_006713959.4:c.985-175dup	N/A	Intron Variant
FBXL5 transcript variant X10	XM_011513831.3:c.934-175d… XM_011513831.3:c.934-175dup	N/A	Intron Variant
FBXL5 transcript variant X17	XM_011513833.3:c.826-175d… XM_011513833.3:c.826-175dup	N/A	Intron Variant
FBXL5 transcript variant X16	XM_017008019.3:c.877-175d… XM_017008019.3:c.877-175dup	N/A	Intron Variant
FBXL5 transcript variant X1	XM_047450049.1:c.985-175d… XM_047450049.1:c.985-175dup	N/A	Intron Variant
FBXL5 transcript variant X2	XM_047450050.1:c.985-175d… XM_047450050.1:c.985-175dup	N/A	Intron Variant
FBXL5 transcript variant X3	XM_047450051.1:c.985-175d… XM_047450051.1:c.985-175dup	N/A	Intron Variant
FBXL5 transcript variant X4	XM_047450052.1:c.985-175d… XM_047450052.1:c.985-175dup	N/A	Intron Variant
FBXL5 transcript variant X6	XM_047450053.1:c.985-175d… XM_047450053.1:c.985-175dup	N/A	Intron Variant
FBXL5 transcript variant X7	XM_047450054.1:c.985-175d… XM_047450054.1:c.985-175dup	N/A	Intron Variant
FBXL5 transcript variant X8	XM_047450055.1:c.985-175d… XM_047450055.1:c.985-175dup	N/A	Intron Variant
FBXL5 transcript variant X9	XM_047450056.1:c.985-175d… XM_047450056.1:c.985-175dup	N/A	Intron Variant
FBXL5 transcript variant X11	XM_047450057.1:c.934-175d… XM_047450057.1:c.934-175dup	N/A	Intron Variant
FBXL5 transcript variant X12	XM_047450058.1:c.934-175d… XM_047450058.1:c.934-175dup	N/A	Intron Variant
FBXL5 transcript variant X13	XM_047450059.1:c.934-175d… XM_047450059.1:c.934-175dup	N/A	Intron Variant
FBXL5 transcript variant X14	XM_047450060.1:c.934-175d… XM_047450060.1:c.934-175dup	N/A	Intron Variant
FBXL5 transcript variant X15	XM_047450061.1:c.877-175d… XM_047450061.1:c.877-175dup	N/A	Intron Variant

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

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	T=	dupT	insTT	insTTT	ins(T)₄	ins(T)₅	ins(T)₇	ins(T)₉	ins(T)₁₁	ins(T)₁₅	ins(T)₁₇	ins(T)₁₈	ins(T)₂₁	ins(T)₂₆
GRCh38.p14 chr 4	NC_000004.12:g.15627130=	NC_000004.12:g.15627130dup	NC_000004.12:g.15627130_15627131insTT	NC_000004.12:g.15627130_15627131insTTT	NC_000004.12:g.15627130_15627131insTTTT	NC_000004.12:g.15627130_15627131insTTTTT	NC_000004.12:g.15627130_15627131insTTTTTTT	NC_000004.12:g.15627130_15627131insTTTTTTTTT	NC_000004.12:g.15627130_15627131insTTTTTTTTTTT	NC_000004.12:g.15627130_15627131insTTTTTTTTTTTTTTT	NC_000004.12:g.15627130_15627131insTTTTTTTTTTTTTTTTT	NC_000004.12:g.15627130_15627131insTTTTTTTTTTTTTTTTTT	NC_000004.12:g.15627130_15627131insTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.15627130_15627131insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.15628753=	NC_000004.11:g.15628753dup	NC_000004.11:g.15628753_15628754insTT	NC_000004.11:g.15628753_15628754insTTT	NC_000004.11:g.15628753_15628754insTTTT	NC_000004.11:g.15628753_15628754insTTTTT	NC_000004.11:g.15628753_15628754insTTTTTTT	NC_000004.11:g.15628753_15628754insTTTTTTTTT	NC_000004.11:g.15628753_15628754insTTTTTTTTTTT	NC_000004.11:g.15628753_15628754insTTTTTTTTTTTTTTT	NC_000004.11:g.15628753_15628754insTTTTTTTTTTTTTTTTT	NC_000004.11:g.15628753_15628754insTTTTTTTTTTTTTTTTTT	NC_000004.11:g.15628753_15628754insTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.15628753_15628754insTTTTTTTTTTTTTTTTTTTTTTTTTT
FBXL5 RefSeqGene	NG_047143.1:g.37788=	NG_047143.1:g.37788dup	NG_047143.1:g.37788_37789insAA	NG_047143.1:g.37788_37789insAAA	NG_047143.1:g.37788_37789insAAAA	NG_047143.1:g.37788_37789insAAAAA	NG_047143.1:g.37788_37789insAAAAAAA	NG_047143.1:g.37788_37789insAAAAAAAAA	NG_047143.1:g.37788_37789insAAAAAAAAAAA	NG_047143.1:g.37788_37789insAAAAAAAAAAAAAAA	NG_047143.1:g.37788_37789insAAAAAAAAAAAAAAAAA	NG_047143.1:g.37788_37789insAAAAAAAAAAAAAAAAAA	NG_047143.1:g.37788_37789insAAAAAAAAAAAAAAAAAAAAA	NG_047143.1:g.37788_37789insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant 3	NM_001193534.1:c.1039-175=	NM_001193534.1:c.1039-175dup	NM_001193534.1:c.1039-175_1039-174insAA	NM_001193534.1:c.1039-175_1039-174insAAA	NM_001193534.1:c.1039-175_1039-174insAAAA	NM_001193534.1:c.1039-175_1039-174insAAAAA	NM_001193534.1:c.1039-175_1039-174insAAAAAAA	NM_001193534.1:c.1039-175_1039-174insAAAAAAAAA	NM_001193534.1:c.1039-175_1039-174insAAAAAAAAAAA	NM_001193534.1:c.1039-175_1039-174insAAAAAAAAAAAAAAA	NM_001193534.1:c.1039-175_1039-174insAAAAAAAAAAAAAAAAA	NM_001193534.1:c.1039-175_1039-174insAAAAAAAAAAAAAAAAAA	NM_001193534.1:c.1039-175_1039-174insAAAAAAAAAAAAAAAAAAAAA	NM_001193534.1:c.1039-175_1039-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant 3	NM_001193534.2:c.1039-175=	NM_001193534.2:c.1039-175dup	NM_001193534.2:c.1039-175_1039-174insAA	NM_001193534.2:c.1039-175_1039-174insAAA	NM_001193534.2:c.1039-175_1039-174insAAAA	NM_001193534.2:c.1039-175_1039-174insAAAAA	NM_001193534.2:c.1039-175_1039-174insAAAAAAA	NM_001193534.2:c.1039-175_1039-174insAAAAAAAAA	NM_001193534.2:c.1039-175_1039-174insAAAAAAAAAAA	NM_001193534.2:c.1039-175_1039-174insAAAAAAAAAAAAAAA	NM_001193534.2:c.1039-175_1039-174insAAAAAAAAAAAAAAAAA	NM_001193534.2:c.1039-175_1039-174insAAAAAAAAAAAAAAAAAA	NM_001193534.2:c.1039-175_1039-174insAAAAAAAAAAAAAAAAAAAAA	NM_001193534.2:c.1039-175_1039-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant 4	NM_001193535.1:c.991-175=	NM_001193535.1:c.991-175dup	NM_001193535.1:c.991-175_991-174insAA	NM_001193535.1:c.991-175_991-174insAAA	NM_001193535.1:c.991-175_991-174insAAAA	NM_001193535.1:c.991-175_991-174insAAAAA	NM_001193535.1:c.991-175_991-174insAAAAAAA	NM_001193535.1:c.991-175_991-174insAAAAAAAAA	NM_001193535.1:c.991-175_991-174insAAAAAAAAAAA	NM_001193535.1:c.991-175_991-174insAAAAAAAAAAAAAAA	NM_001193535.1:c.991-175_991-174insAAAAAAAAAAAAAAAAA	NM_001193535.1:c.991-175_991-174insAAAAAAAAAAAAAAAAAA	NM_001193535.1:c.991-175_991-174insAAAAAAAAAAAAAAAAAAAAA	NM_001193535.1:c.991-175_991-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant 4	NM_001193535.2:c.991-175=	NM_001193535.2:c.991-175dup	NM_001193535.2:c.991-175_991-174insAA	NM_001193535.2:c.991-175_991-174insAAA	NM_001193535.2:c.991-175_991-174insAAAA	NM_001193535.2:c.991-175_991-174insAAAAA	NM_001193535.2:c.991-175_991-174insAAAAAAA	NM_001193535.2:c.991-175_991-174insAAAAAAAAA	NM_001193535.2:c.991-175_991-174insAAAAAAAAAAA	NM_001193535.2:c.991-175_991-174insAAAAAAAAAAAAAAA	NM_001193535.2:c.991-175_991-174insAAAAAAAAAAAAAAAAA	NM_001193535.2:c.991-175_991-174insAAAAAAAAAAAAAAAAAA	NM_001193535.2:c.991-175_991-174insAAAAAAAAAAAAAAAAAAAAA	NM_001193535.2:c.991-175_991-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant 1	NM_012161.3:c.1042-175=	NM_012161.3:c.1042-175dup	NM_012161.3:c.1042-175_1042-174insAA	NM_012161.3:c.1042-175_1042-174insAAA	NM_012161.3:c.1042-175_1042-174insAAAA	NM_012161.3:c.1042-175_1042-174insAAAAA	NM_012161.3:c.1042-175_1042-174insAAAAAAA	NM_012161.3:c.1042-175_1042-174insAAAAAAAAA	NM_012161.3:c.1042-175_1042-174insAAAAAAAAAAA	NM_012161.3:c.1042-175_1042-174insAAAAAAAAAAAAAAA	NM_012161.3:c.1042-175_1042-174insAAAAAAAAAAAAAAAAA	NM_012161.3:c.1042-175_1042-174insAAAAAAAAAAAAAAAAAA	NM_012161.3:c.1042-175_1042-174insAAAAAAAAAAAAAAAAAAAAA	NM_012161.3:c.1042-175_1042-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant 1	NM_012161.4:c.1042-175=	NM_012161.4:c.1042-175dup	NM_012161.4:c.1042-175_1042-174insAA	NM_012161.4:c.1042-175_1042-174insAAA	NM_012161.4:c.1042-175_1042-174insAAAA	NM_012161.4:c.1042-175_1042-174insAAAAA	NM_012161.4:c.1042-175_1042-174insAAAAAAA	NM_012161.4:c.1042-175_1042-174insAAAAAAAAA	NM_012161.4:c.1042-175_1042-174insAAAAAAAAAAA	NM_012161.4:c.1042-175_1042-174insAAAAAAAAAAAAAAA	NM_012161.4:c.1042-175_1042-174insAAAAAAAAAAAAAAAAA	NM_012161.4:c.1042-175_1042-174insAAAAAAAAAAAAAAAAAA	NM_012161.4:c.1042-175_1042-174insAAAAAAAAAAAAAAAAAAAAA	NM_012161.4:c.1042-175_1042-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X1	XM_005248152.1:c.877-175=	XM_005248152.1:c.877-175dup	XM_005248152.1:c.877-175_877-174insAA	XM_005248152.1:c.877-175_877-174insAAA	XM_005248152.1:c.877-175_877-174insAAAA	XM_005248152.1:c.877-175_877-174insAAAAA	XM_005248152.1:c.877-175_877-174insAAAAAAA	XM_005248152.1:c.877-175_877-174insAAAAAAAAA	XM_005248152.1:c.877-175_877-174insAAAAAAAAAAA	XM_005248152.1:c.877-175_877-174insAAAAAAAAAAAAAAA	XM_005248152.1:c.877-175_877-174insAAAAAAAAAAAAAAAAA	XM_005248152.1:c.877-175_877-174insAAAAAAAAAAAAAAAAAA	XM_005248152.1:c.877-175_877-174insAAAAAAAAAAAAAAAAAAAAA	XM_005248152.1:c.877-175_877-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X2	XM_005248153.1:c.664-175=	XM_005248153.1:c.664-175dup	XM_005248153.1:c.664-175_664-174insAA	XM_005248153.1:c.664-175_664-174insAAA	XM_005248153.1:c.664-175_664-174insAAAA	XM_005248153.1:c.664-175_664-174insAAAAA	XM_005248153.1:c.664-175_664-174insAAAAAAA	XM_005248153.1:c.664-175_664-174insAAAAAAAAA	XM_005248153.1:c.664-175_664-174insAAAAAAAAAAA	XM_005248153.1:c.664-175_664-174insAAAAAAAAAAAAAAA	XM_005248153.1:c.664-175_664-174insAAAAAAAAAAAAAAAAA	XM_005248153.1:c.664-175_664-174insAAAAAAAAAAAAAAAAAA	XM_005248153.1:c.664-175_664-174insAAAAAAAAAAAAAAAAAAAAA	XM_005248153.1:c.664-175_664-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X5	XM_006713959.4:c.985-175=	XM_006713959.4:c.985-175dup	XM_006713959.4:c.985-175_985-174insAA	XM_006713959.4:c.985-175_985-174insAAA	XM_006713959.4:c.985-175_985-174insAAAA	XM_006713959.4:c.985-175_985-174insAAAAA	XM_006713959.4:c.985-175_985-174insAAAAAAA	XM_006713959.4:c.985-175_985-174insAAAAAAAAA	XM_006713959.4:c.985-175_985-174insAAAAAAAAAAA	XM_006713959.4:c.985-175_985-174insAAAAAAAAAAAAAAA	XM_006713959.4:c.985-175_985-174insAAAAAAAAAAAAAAAAA	XM_006713959.4:c.985-175_985-174insAAAAAAAAAAAAAAAAAA	XM_006713959.4:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAA	XM_006713959.4:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X10	XM_011513831.3:c.934-175=	XM_011513831.3:c.934-175dup	XM_011513831.3:c.934-175_934-174insAA	XM_011513831.3:c.934-175_934-174insAAA	XM_011513831.3:c.934-175_934-174insAAAA	XM_011513831.3:c.934-175_934-174insAAAAA	XM_011513831.3:c.934-175_934-174insAAAAAAA	XM_011513831.3:c.934-175_934-174insAAAAAAAAA	XM_011513831.3:c.934-175_934-174insAAAAAAAAAAA	XM_011513831.3:c.934-175_934-174insAAAAAAAAAAAAAAA	XM_011513831.3:c.934-175_934-174insAAAAAAAAAAAAAAAAA	XM_011513831.3:c.934-175_934-174insAAAAAAAAAAAAAAAAAA	XM_011513831.3:c.934-175_934-174insAAAAAAAAAAAAAAAAAAAAA	XM_011513831.3:c.934-175_934-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X17	XM_011513833.3:c.826-175=	XM_011513833.3:c.826-175dup	XM_011513833.3:c.826-175_826-174insAA	XM_011513833.3:c.826-175_826-174insAAA	XM_011513833.3:c.826-175_826-174insAAAA	XM_011513833.3:c.826-175_826-174insAAAAA	XM_011513833.3:c.826-175_826-174insAAAAAAA	XM_011513833.3:c.826-175_826-174insAAAAAAAAA	XM_011513833.3:c.826-175_826-174insAAAAAAAAAAA	XM_011513833.3:c.826-175_826-174insAAAAAAAAAAAAAAA	XM_011513833.3:c.826-175_826-174insAAAAAAAAAAAAAAAAA	XM_011513833.3:c.826-175_826-174insAAAAAAAAAAAAAAAAAA	XM_011513833.3:c.826-175_826-174insAAAAAAAAAAAAAAAAAAAAA	XM_011513833.3:c.826-175_826-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X16	XM_017008019.3:c.877-175=	XM_017008019.3:c.877-175dup	XM_017008019.3:c.877-175_877-174insAA	XM_017008019.3:c.877-175_877-174insAAA	XM_017008019.3:c.877-175_877-174insAAAA	XM_017008019.3:c.877-175_877-174insAAAAA	XM_017008019.3:c.877-175_877-174insAAAAAAA	XM_017008019.3:c.877-175_877-174insAAAAAAAAA	XM_017008019.3:c.877-175_877-174insAAAAAAAAAAA	XM_017008019.3:c.877-175_877-174insAAAAAAAAAAAAAAA	XM_017008019.3:c.877-175_877-174insAAAAAAAAAAAAAAAAA	XM_017008019.3:c.877-175_877-174insAAAAAAAAAAAAAAAAAA	XM_017008019.3:c.877-175_877-174insAAAAAAAAAAAAAAAAAAAAA	XM_017008019.3:c.877-175_877-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X1	XM_047450049.1:c.985-175=	XM_047450049.1:c.985-175dup	XM_047450049.1:c.985-175_985-174insAA	XM_047450049.1:c.985-175_985-174insAAA	XM_047450049.1:c.985-175_985-174insAAAA	XM_047450049.1:c.985-175_985-174insAAAAA	XM_047450049.1:c.985-175_985-174insAAAAAAA	XM_047450049.1:c.985-175_985-174insAAAAAAAAA	XM_047450049.1:c.985-175_985-174insAAAAAAAAAAA	XM_047450049.1:c.985-175_985-174insAAAAAAAAAAAAAAA	XM_047450049.1:c.985-175_985-174insAAAAAAAAAAAAAAAAA	XM_047450049.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAA	XM_047450049.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450049.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X2	XM_047450050.1:c.985-175=	XM_047450050.1:c.985-175dup	XM_047450050.1:c.985-175_985-174insAA	XM_047450050.1:c.985-175_985-174insAAA	XM_047450050.1:c.985-175_985-174insAAAA	XM_047450050.1:c.985-175_985-174insAAAAA	XM_047450050.1:c.985-175_985-174insAAAAAAA	XM_047450050.1:c.985-175_985-174insAAAAAAAAA	XM_047450050.1:c.985-175_985-174insAAAAAAAAAAA	XM_047450050.1:c.985-175_985-174insAAAAAAAAAAAAAAA	XM_047450050.1:c.985-175_985-174insAAAAAAAAAAAAAAAAA	XM_047450050.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAA	XM_047450050.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450050.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X3	XM_047450051.1:c.985-175=	XM_047450051.1:c.985-175dup	XM_047450051.1:c.985-175_985-174insAA	XM_047450051.1:c.985-175_985-174insAAA	XM_047450051.1:c.985-175_985-174insAAAA	XM_047450051.1:c.985-175_985-174insAAAAA	XM_047450051.1:c.985-175_985-174insAAAAAAA	XM_047450051.1:c.985-175_985-174insAAAAAAAAA	XM_047450051.1:c.985-175_985-174insAAAAAAAAAAA	XM_047450051.1:c.985-175_985-174insAAAAAAAAAAAAAAA	XM_047450051.1:c.985-175_985-174insAAAAAAAAAAAAAAAAA	XM_047450051.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAA	XM_047450051.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450051.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X4	XM_047450052.1:c.985-175=	XM_047450052.1:c.985-175dup	XM_047450052.1:c.985-175_985-174insAA	XM_047450052.1:c.985-175_985-174insAAA	XM_047450052.1:c.985-175_985-174insAAAA	XM_047450052.1:c.985-175_985-174insAAAAA	XM_047450052.1:c.985-175_985-174insAAAAAAA	XM_047450052.1:c.985-175_985-174insAAAAAAAAA	XM_047450052.1:c.985-175_985-174insAAAAAAAAAAA	XM_047450052.1:c.985-175_985-174insAAAAAAAAAAAAAAA	XM_047450052.1:c.985-175_985-174insAAAAAAAAAAAAAAAAA	XM_047450052.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAA	XM_047450052.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450052.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X6	XM_047450053.1:c.985-175=	XM_047450053.1:c.985-175dup	XM_047450053.1:c.985-175_985-174insAA	XM_047450053.1:c.985-175_985-174insAAA	XM_047450053.1:c.985-175_985-174insAAAA	XM_047450053.1:c.985-175_985-174insAAAAA	XM_047450053.1:c.985-175_985-174insAAAAAAA	XM_047450053.1:c.985-175_985-174insAAAAAAAAA	XM_047450053.1:c.985-175_985-174insAAAAAAAAAAA	XM_047450053.1:c.985-175_985-174insAAAAAAAAAAAAAAA	XM_047450053.1:c.985-175_985-174insAAAAAAAAAAAAAAAAA	XM_047450053.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAA	XM_047450053.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450053.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X7	XM_047450054.1:c.985-175=	XM_047450054.1:c.985-175dup	XM_047450054.1:c.985-175_985-174insAA	XM_047450054.1:c.985-175_985-174insAAA	XM_047450054.1:c.985-175_985-174insAAAA	XM_047450054.1:c.985-175_985-174insAAAAA	XM_047450054.1:c.985-175_985-174insAAAAAAA	XM_047450054.1:c.985-175_985-174insAAAAAAAAA	XM_047450054.1:c.985-175_985-174insAAAAAAAAAAA	XM_047450054.1:c.985-175_985-174insAAAAAAAAAAAAAAA	XM_047450054.1:c.985-175_985-174insAAAAAAAAAAAAAAAAA	XM_047450054.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAA	XM_047450054.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450054.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X8	XM_047450055.1:c.985-175=	XM_047450055.1:c.985-175dup	XM_047450055.1:c.985-175_985-174insAA	XM_047450055.1:c.985-175_985-174insAAA	XM_047450055.1:c.985-175_985-174insAAAA	XM_047450055.1:c.985-175_985-174insAAAAA	XM_047450055.1:c.985-175_985-174insAAAAAAA	XM_047450055.1:c.985-175_985-174insAAAAAAAAA	XM_047450055.1:c.985-175_985-174insAAAAAAAAAAA	XM_047450055.1:c.985-175_985-174insAAAAAAAAAAAAAAA	XM_047450055.1:c.985-175_985-174insAAAAAAAAAAAAAAAAA	XM_047450055.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAA	XM_047450055.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450055.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X9	XM_047450056.1:c.985-175=	XM_047450056.1:c.985-175dup	XM_047450056.1:c.985-175_985-174insAA	XM_047450056.1:c.985-175_985-174insAAA	XM_047450056.1:c.985-175_985-174insAAAA	XM_047450056.1:c.985-175_985-174insAAAAA	XM_047450056.1:c.985-175_985-174insAAAAAAA	XM_047450056.1:c.985-175_985-174insAAAAAAAAA	XM_047450056.1:c.985-175_985-174insAAAAAAAAAAA	XM_047450056.1:c.985-175_985-174insAAAAAAAAAAAAAAA	XM_047450056.1:c.985-175_985-174insAAAAAAAAAAAAAAAAA	XM_047450056.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAA	XM_047450056.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450056.1:c.985-175_985-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X11	XM_047450057.1:c.934-175=	XM_047450057.1:c.934-175dup	XM_047450057.1:c.934-175_934-174insAA	XM_047450057.1:c.934-175_934-174insAAA	XM_047450057.1:c.934-175_934-174insAAAA	XM_047450057.1:c.934-175_934-174insAAAAA	XM_047450057.1:c.934-175_934-174insAAAAAAA	XM_047450057.1:c.934-175_934-174insAAAAAAAAA	XM_047450057.1:c.934-175_934-174insAAAAAAAAAAA	XM_047450057.1:c.934-175_934-174insAAAAAAAAAAAAAAA	XM_047450057.1:c.934-175_934-174insAAAAAAAAAAAAAAAAA	XM_047450057.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAA	XM_047450057.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450057.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X12	XM_047450058.1:c.934-175=	XM_047450058.1:c.934-175dup	XM_047450058.1:c.934-175_934-174insAA	XM_047450058.1:c.934-175_934-174insAAA	XM_047450058.1:c.934-175_934-174insAAAA	XM_047450058.1:c.934-175_934-174insAAAAA	XM_047450058.1:c.934-175_934-174insAAAAAAA	XM_047450058.1:c.934-175_934-174insAAAAAAAAA	XM_047450058.1:c.934-175_934-174insAAAAAAAAAAA	XM_047450058.1:c.934-175_934-174insAAAAAAAAAAAAAAA	XM_047450058.1:c.934-175_934-174insAAAAAAAAAAAAAAAAA	XM_047450058.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAA	XM_047450058.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450058.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X13	XM_047450059.1:c.934-175=	XM_047450059.1:c.934-175dup	XM_047450059.1:c.934-175_934-174insAA	XM_047450059.1:c.934-175_934-174insAAA	XM_047450059.1:c.934-175_934-174insAAAA	XM_047450059.1:c.934-175_934-174insAAAAA	XM_047450059.1:c.934-175_934-174insAAAAAAA	XM_047450059.1:c.934-175_934-174insAAAAAAAAA	XM_047450059.1:c.934-175_934-174insAAAAAAAAAAA	XM_047450059.1:c.934-175_934-174insAAAAAAAAAAAAAAA	XM_047450059.1:c.934-175_934-174insAAAAAAAAAAAAAAAAA	XM_047450059.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAA	XM_047450059.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450059.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X14	XM_047450060.1:c.934-175=	XM_047450060.1:c.934-175dup	XM_047450060.1:c.934-175_934-174insAA	XM_047450060.1:c.934-175_934-174insAAA	XM_047450060.1:c.934-175_934-174insAAAA	XM_047450060.1:c.934-175_934-174insAAAAA	XM_047450060.1:c.934-175_934-174insAAAAAAA	XM_047450060.1:c.934-175_934-174insAAAAAAAAA	XM_047450060.1:c.934-175_934-174insAAAAAAAAAAA	XM_047450060.1:c.934-175_934-174insAAAAAAAAAAAAAAA	XM_047450060.1:c.934-175_934-174insAAAAAAAAAAAAAAAAA	XM_047450060.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAA	XM_047450060.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450060.1:c.934-175_934-174insAAAAAAAAAAAAAAAAAAAAAAAAAA
FBXL5 transcript variant X15	XM_047450061.1:c.877-175=	XM_047450061.1:c.877-175dup	XM_047450061.1:c.877-175_877-174insAA	XM_047450061.1:c.877-175_877-174insAAA	XM_047450061.1:c.877-175_877-174insAAAA	XM_047450061.1:c.877-175_877-174insAAAAA	XM_047450061.1:c.877-175_877-174insAAAAAAA	XM_047450061.1:c.877-175_877-174insAAAAAAAAA	XM_047450061.1:c.877-175_877-174insAAAAAAAAAAA	XM_047450061.1:c.877-175_877-174insAAAAAAAAAAAAAAA	XM_047450061.1:c.877-175_877-174insAAAAAAAAAAAAAAAAA	XM_047450061.1:c.877-175_877-174insAAAAAAAAAAAAAAAAAA	XM_047450061.1:c.877-175_877-174insAAAAAAAAAAAAAAAAAAAAA	XM_047450061.1:c.877-175_877-174insAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

15 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ACPOP	ss3730891364	Jul 13, 2019 (153)
2	ACPOP	ss3730891365	Jul 13, 2019 (153)
3	ACPOP	ss3730891366	Jul 13, 2019 (153)
4	GNOMAD	ss4091236110	Apr 26, 2021 (155)
5	GNOMAD	ss4091236111	Apr 26, 2021 (155)
6	GNOMAD	ss4091236112	Apr 26, 2021 (155)
7	GNOMAD	ss4091236113	Apr 26, 2021 (155)
8	GNOMAD	ss4091236114	Apr 26, 2021 (155)
9	GNOMAD	ss4091236115	Apr 26, 2021 (155)
10	GNOMAD	ss4091236116	Apr 26, 2021 (155)
11	GNOMAD	ss4091236117	Apr 26, 2021 (155)
12	GNOMAD	ss4091236118	Apr 26, 2021 (155)
13	GNOMAD	ss4091236119	Apr 26, 2021 (155)
14	GNOMAD	ss4091236120	Apr 26, 2021 (155)
15	HUGCELL_USP	ss5457069253	Oct 17, 2022 (156)
16	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141369054 (NC_000004.12:15627129::T 67/79220) Row 141369055 (NC_000004.12:15627129::TT 10/79242) Row 141369056 (NC_000004.12:15627129::TTT 5/79250)...	-	Apr 26, 2021 (155)
17	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141369054 (NC_000004.12:15627129::T 67/79220) Row 141369055 (NC_000004.12:15627129::TT 10/79242) Row 141369056 (NC_000004.12:15627129::TTT 5/79250)...	-	Apr 26, 2021 (155)
18	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141369054 (NC_000004.12:15627129::T 67/79220) Row 141369055 (NC_000004.12:15627129::TT 10/79242) Row 141369056 (NC_000004.12:15627129::TTT 5/79250)...	-	Apr 26, 2021 (155)
19	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141369054 (NC_000004.12:15627129::T 67/79220) Row 141369055 (NC_000004.12:15627129::TT 10/79242) Row 141369056 (NC_000004.12:15627129::TTT 5/79250)...	-	Apr 26, 2021 (155)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141369054 (NC_000004.12:15627129::T 67/79220) Row 141369055 (NC_000004.12:15627129::TT 10/79242) Row 141369056 (NC_000004.12:15627129::TTT 5/79250)...	-	Apr 26, 2021 (155)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141369054 (NC_000004.12:15627129::T 67/79220) Row 141369055 (NC_000004.12:15627129::TT 10/79242) Row 141369056 (NC_000004.12:15627129::TTT 5/79250)...	-	Apr 26, 2021 (155)
22	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141369054 (NC_000004.12:15627129::T 67/79220) Row 141369055 (NC_000004.12:15627129::TT 10/79242) Row 141369056 (NC_000004.12:15627129::TTT 5/79250)...	-	Apr 26, 2021 (155)
23	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141369054 (NC_000004.12:15627129::T 67/79220) Row 141369055 (NC_000004.12:15627129::TT 10/79242) Row 141369056 (NC_000004.12:15627129::TTT 5/79250)...	-	Apr 26, 2021 (155)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141369054 (NC_000004.12:15627129::T 67/79220) Row 141369055 (NC_000004.12:15627129::TT 10/79242) Row 141369056 (NC_000004.12:15627129::TTT 5/79250)...	-	Apr 26, 2021 (155)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141369054 (NC_000004.12:15627129::T 67/79220) Row 141369055 (NC_000004.12:15627129::TT 10/79242) Row 141369056 (NC_000004.12:15627129::TTT 5/79250)...	-	Apr 26, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 141369054 (NC_000004.12:15627129::T 67/79220) Row 141369055 (NC_000004.12:15627129::TT 10/79242) Row 141369056 (NC_000004.12:15627129::TTT 5/79250)...	-	Apr 26, 2021 (155)
27	Northern Sweden Submission ignored due to conflicting rows: Row 4176229 (NC_000004.11:15628752::TTTTTTT 3/550) Row 4176230 (NC_000004.11:15628752::TTTTTTTTTTT 2/550) Row 4176231 (NC_000004.11:15628752::TTTTTTTTTTTTTTTTTT 1/550)	-	Jul 13, 2019 (153)
28	Northern Sweden Submission ignored due to conflicting rows: Row 4176229 (NC_000004.11:15628752::TTTTTTT 3/550) Row 4176230 (NC_000004.11:15628752::TTTTTTTTTTT 2/550) Row 4176231 (NC_000004.11:15628752::TTTTTTTTTTTTTTTTTT 1/550)	-	Jul 13, 2019 (153)
29	Northern Sweden Submission ignored due to conflicting rows: Row 4176229 (NC_000004.11:15628752::TTTTTTT 3/550) Row 4176230 (NC_000004.11:15628752::TTTTTTTTTTT 2/550) Row 4176231 (NC_000004.11:15628752::TTTTTTTTTTTTTTTTTT 1/550)	-	Jul 13, 2019 (153)
30	ALFA	NC_000004.12 - 15627130	Apr 26, 2021 (155)

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
ss4091236110, ss5457069253	NC_000004.12:15627129::T	NC_000004.12:15627129:T:TT	(self)
5297932684	NC_000004.12:15627129:T:TT	NC_000004.12:15627129:T:TT	(self)
ss4091236111	NC_000004.12:15627129::TT	NC_000004.12:15627129:T:TTT	(self)
ss4091236112	NC_000004.12:15627129::TTT	NC_000004.12:15627129:T:TTTT	(self)
ss4091236113	NC_000004.12:15627129::TTTT	NC_000004.12:15627129:T:TTTTT	(self)
ss4091236114	NC_000004.12:15627129::TTTTT	NC_000004.12:15627129:T:TTTTTT	(self)
ss3730891364	NC_000004.11:15628752::TTTTTTT	NC_000004.12:15627129:T:TTTTTTTT	(self)
ss4091236115	NC_000004.12:15627129::TTTTTTT	NC_000004.12:15627129:T:TTTTTTTT	(self)
ss4091236116	NC_000004.12:15627129::TTTTTTTTT	NC_000004.12:15627129:T:TTTTTTTTTT	(self)
ss3730891365	NC_000004.11:15628752::TTTTTTTTTTT	NC_000004.12:15627129:T:TTTTTTTTTT… NC_000004.12:15627129:T:TTTTTTTTTTTT	(self)
ss4091236117	NC_000004.12:15627129::TTTTTTTTTTT… NC_000004.12:15627129::TTTTTTTTTTTTTTT	NC_000004.12:15627129:T:TTTTTTTTTT… NC_000004.12:15627129:T:TTTTTTTTTTTTTTTT	(self)
ss4091236118	NC_000004.12:15627129::TTTTTTTTTTT… NC_000004.12:15627129::TTTTTTTTTTTTTTTTT	NC_000004.12:15627129:T:TTTTTTTTTT… NC_000004.12:15627129:T:TTTTTTTTTTTTTTTTTT	(self)
ss3730891366	NC_000004.11:15628752::TTTTTTTTTTT… NC_000004.11:15628752::TTTTTTTTTTTTTTTTTT	NC_000004.12:15627129:T:TTTTTTTTTT… NC_000004.12:15627129:T:TTTTTTTTTTTTTTTTTTT	(self)
ss4091236119	NC_000004.12:15627129::TTTTTTTTTTT… NC_000004.12:15627129::TTTTTTTTTTTTTTTTTTTTT	NC_000004.12:15627129:T:TTTTTTTTTT… NC_000004.12:15627129:T:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4091236120	NC_000004.12:15627129::TTTTTTTTTTT… NC_000004.12:15627129::TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:15627129:T:TTTTTTTTTT… NC_000004.12:15627129:T:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1491071832

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491071832