Name: rs1168037153
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.

rs1168037153

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:184917369-184917393 (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(T)₁₃ / del(T)₁₂ / del(T)₅ / de…
del(T)₁₃ / del(T)₁₂ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.3087 (1527/4946, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NIBAN1 : 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	4946	TTTTTTTTTTTTTTTTTTTTTTTTT=0.4402	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.3087, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.2311, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0158, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0020, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0022, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.531491	0.23072	0.237789	32
European	Sub	4642	TTTTTTTTTTTTTTTTTTTTTTTTT=0.4050	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.3277, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.2460, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0168, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0022, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0024, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.483274	0.253381	0.263345	32
African	Sub	222	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	210	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	42	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	38	TTTTTTTTTTTTTTTTTTTTTTTTT=0.82	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.16, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.833333	0.166667	0.0	10

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	4946	(T)₂₅=0.4402	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.3087, dupT=0.2311, dupTT=0.0158, dupTTT=0.0020, dup(T)₄=0.0022, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000
Allele Frequency Aggregator	European	Sub	4642	(T)₂₅=0.4050	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.3277, dupT=0.2460, dupTT=0.0168, dupTTT=0.0022, dup(T)₄=0.0024, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000
Allele Frequency Aggregator	African	Sub	222	(T)₂₅=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Latin American 2	Sub	42	(T)₂₅=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	Other	Sub	38	(T)₂₅=0.82	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.16, dupT=0.03, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	Asian	Sub	2	(T)₂₅=1.0	del(T)₁₃=0.0, del(T)₁₂=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0, dup(T)₈=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₂₅=0	del(T)₁₃=0, del(T)₁₂=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0, dup(T)₈=0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₂₅=0	del(T)₁₃=0, del(T)₁₂=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0, dup(T)₈=0

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.184917381_184917393del
GRCh38.p14 chr 1	NC_000001.11:g.184917382_184917393del
GRCh38.p14 chr 1	NC_000001.11:g.184917389_184917393del
GRCh38.p14 chr 1	NC_000001.11:g.184917390_184917393del
GRCh38.p14 chr 1	NC_000001.11:g.184917391_184917393del
GRCh38.p14 chr 1	NC_000001.11:g.184917392_184917393del
GRCh38.p14 chr 1	NC_000001.11:g.184917393del
GRCh38.p14 chr 1	NC_000001.11:g.184917393dup
GRCh38.p14 chr 1	NC_000001.11:g.184917392_184917393dup
GRCh38.p14 chr 1	NC_000001.11:g.184917391_184917393dup
GRCh38.p14 chr 1	NC_000001.11:g.184917390_184917393dup
GRCh38.p14 chr 1	NC_000001.11:g.184917389_184917393dup
GRCh38.p14 chr 1	NC_000001.11:g.184917388_184917393dup
GRCh38.p14 chr 1	NC_000001.11:g.184917387_184917393dup
GRCh38.p14 chr 1	NC_000001.11:g.184917386_184917393dup
GRCh37.p13 chr 1	NC_000001.10:g.184886514_184886526del
GRCh37.p13 chr 1	NC_000001.10:g.184886515_184886526del
GRCh37.p13 chr 1	NC_000001.10:g.184886522_184886526del
GRCh37.p13 chr 1	NC_000001.10:g.184886523_184886526del
GRCh37.p13 chr 1	NC_000001.10:g.184886524_184886526del
GRCh37.p13 chr 1	NC_000001.10:g.184886525_184886526del
GRCh37.p13 chr 1	NC_000001.10:g.184886526del
GRCh37.p13 chr 1	NC_000001.10:g.184886526dup
GRCh37.p13 chr 1	NC_000001.10:g.184886525_184886526dup
GRCh37.p13 chr 1	NC_000001.10:g.184886524_184886526dup
GRCh37.p13 chr 1	NC_000001.10:g.184886523_184886526dup
GRCh37.p13 chr 1	NC_000001.10:g.184886522_184886526dup
GRCh37.p13 chr 1	NC_000001.10:g.184886521_184886526dup
GRCh37.p13 chr 1	NC_000001.10:g.184886520_184886526dup
GRCh37.p13 chr 1	NC_000001.10:g.184886519_184886526dup
NIBAN1 RefSeqGene	NG_051588.1:g.62206_62218del
NIBAN1 RefSeqGene	NG_051588.1:g.62207_62218del
NIBAN1 RefSeqGene	NG_051588.1:g.62214_62218del
NIBAN1 RefSeqGene	NG_051588.1:g.62215_62218del
NIBAN1 RefSeqGene	NG_051588.1:g.62216_62218del
NIBAN1 RefSeqGene	NG_051588.1:g.62217_62218del
NIBAN1 RefSeqGene	NG_051588.1:g.62218del
NIBAN1 RefSeqGene	NG_051588.1:g.62218dup
NIBAN1 RefSeqGene	NG_051588.1:g.62217_62218dup
NIBAN1 RefSeqGene	NG_051588.1:g.62216_62218dup
NIBAN1 RefSeqGene	NG_051588.1:g.62215_62218dup
NIBAN1 RefSeqGene	NG_051588.1:g.62214_62218dup
NIBAN1 RefSeqGene	NG_051588.1:g.62213_62218dup
NIBAN1 RefSeqGene	NG_051588.1:g.62212_62218dup
NIBAN1 RefSeqGene	NG_051588.1:g.62211_62218dup

Gene: NIBAN1, niban apoptosis regulator 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NIBAN1 transcript	NM_052966.4:c.56-18072_56… NM_052966.4:c.56-18072_56-18060del	N/A	Intron Variant
NIBAN1 transcript variant X1	XM_047444091.1:c.233-1807… XM_047444091.1:c.233-18072_233-18060del	N/A	Intron Variant
NIBAN1 transcript variant X2	XM_047444093.1:c.233-1807… XM_047444093.1:c.233-18072_233-18060del	N/A	Intron Variant
NIBAN1 transcript variant X3	XM_047444094.1:c.233-1807… XM_047444094.1:c.233-18072_233-18060del	N/A	Intron Variant
NIBAN1 transcript variant X4	XM_047444098.1:c.56-18072… XM_047444098.1:c.56-18072_56-18060del	N/A	Intron Variant
NIBAN1 transcript variant X5	XM_047444102.1:c.56-18072… XM_047444102.1:c.56-18072_56-18060del	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)₂₅=	del(T)₁₃	del(T)₁₂	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈
GRCh38.p14 chr 1	NC_000001.11:g.184917369_184917393=	NC_000001.11:g.184917381_184917393del	NC_000001.11:g.184917382_184917393del	NC_000001.11:g.184917389_184917393del	NC_000001.11:g.184917390_184917393del	NC_000001.11:g.184917391_184917393del	NC_000001.11:g.184917392_184917393del	NC_000001.11:g.184917393del	NC_000001.11:g.184917393dup	NC_000001.11:g.184917392_184917393dup	NC_000001.11:g.184917391_184917393dup	NC_000001.11:g.184917390_184917393dup	NC_000001.11:g.184917389_184917393dup	NC_000001.11:g.184917388_184917393dup	NC_000001.11:g.184917387_184917393dup	NC_000001.11:g.184917386_184917393dup
GRCh37.p13 chr 1	NC_000001.10:g.184886502_184886526=	NC_000001.10:g.184886514_184886526del	NC_000001.10:g.184886515_184886526del	NC_000001.10:g.184886522_184886526del	NC_000001.10:g.184886523_184886526del	NC_000001.10:g.184886524_184886526del	NC_000001.10:g.184886525_184886526del	NC_000001.10:g.184886526del	NC_000001.10:g.184886526dup	NC_000001.10:g.184886525_184886526dup	NC_000001.10:g.184886524_184886526dup	NC_000001.10:g.184886523_184886526dup	NC_000001.10:g.184886522_184886526dup	NC_000001.10:g.184886521_184886526dup	NC_000001.10:g.184886520_184886526dup	NC_000001.10:g.184886519_184886526dup
NIBAN1 RefSeqGene	NG_051588.1:g.62194_62218=	NG_051588.1:g.62206_62218del	NG_051588.1:g.62207_62218del	NG_051588.1:g.62214_62218del	NG_051588.1:g.62215_62218del	NG_051588.1:g.62216_62218del	NG_051588.1:g.62217_62218del	NG_051588.1:g.62218del	NG_051588.1:g.62218dup	NG_051588.1:g.62217_62218dup	NG_051588.1:g.62216_62218dup	NG_051588.1:g.62215_62218dup	NG_051588.1:g.62214_62218dup	NG_051588.1:g.62213_62218dup	NG_051588.1:g.62212_62218dup	NG_051588.1:g.62211_62218dup
FAM129A transcript	NM_052966.3:c.56-18060=	NM_052966.3:c.56-18072_56-18060del	NM_052966.3:c.56-18071_56-18060del	NM_052966.3:c.56-18064_56-18060del	NM_052966.3:c.56-18063_56-18060del	NM_052966.3:c.56-18062_56-18060del	NM_052966.3:c.56-18061_56-18060del	NM_052966.3:c.56-18060del	NM_052966.3:c.56-18060dup	NM_052966.3:c.56-18061_56-18060dup	NM_052966.3:c.56-18062_56-18060dup	NM_052966.3:c.56-18063_56-18060dup	NM_052966.3:c.56-18064_56-18060dup	NM_052966.3:c.56-18065_56-18060dup	NM_052966.3:c.56-18066_56-18060dup	NM_052966.3:c.56-18067_56-18060dup
NIBAN1 transcript	NM_052966.4:c.56-18060=	NM_052966.4:c.56-18072_56-18060del	NM_052966.4:c.56-18071_56-18060del	NM_052966.4:c.56-18064_56-18060del	NM_052966.4:c.56-18063_56-18060del	NM_052966.4:c.56-18062_56-18060del	NM_052966.4:c.56-18061_56-18060del	NM_052966.4:c.56-18060del	NM_052966.4:c.56-18060dup	NM_052966.4:c.56-18061_56-18060dup	NM_052966.4:c.56-18062_56-18060dup	NM_052966.4:c.56-18063_56-18060dup	NM_052966.4:c.56-18064_56-18060dup	NM_052966.4:c.56-18065_56-18060dup	NM_052966.4:c.56-18066_56-18060dup	NM_052966.4:c.56-18067_56-18060dup
FAM129A transcript variant X1	XM_005244873.1:c.56-18060=	XM_005244873.1:c.56-18072_56-18060del	XM_005244873.1:c.56-18071_56-18060del	XM_005244873.1:c.56-18064_56-18060del	XM_005244873.1:c.56-18063_56-18060del	XM_005244873.1:c.56-18062_56-18060del	XM_005244873.1:c.56-18061_56-18060del	XM_005244873.1:c.56-18060del	XM_005244873.1:c.56-18060dup	XM_005244873.1:c.56-18061_56-18060dup	XM_005244873.1:c.56-18062_56-18060dup	XM_005244873.1:c.56-18063_56-18060dup	XM_005244873.1:c.56-18064_56-18060dup	XM_005244873.1:c.56-18065_56-18060dup	XM_005244873.1:c.56-18066_56-18060dup	XM_005244873.1:c.56-18067_56-18060dup
NIBAN1 transcript variant X1	XM_047444091.1:c.233-18060=	XM_047444091.1:c.233-18072_233-18060del	XM_047444091.1:c.233-18071_233-18060del	XM_047444091.1:c.233-18064_233-18060del	XM_047444091.1:c.233-18063_233-18060del	XM_047444091.1:c.233-18062_233-18060del	XM_047444091.1:c.233-18061_233-18060del	XM_047444091.1:c.233-18060del	XM_047444091.1:c.233-18060dup	XM_047444091.1:c.233-18061_233-18060dup	XM_047444091.1:c.233-18062_233-18060dup	XM_047444091.1:c.233-18063_233-18060dup	XM_047444091.1:c.233-18064_233-18060dup	XM_047444091.1:c.233-18065_233-18060dup	XM_047444091.1:c.233-18066_233-18060dup	XM_047444091.1:c.233-18067_233-18060dup
NIBAN1 transcript variant X2	XM_047444093.1:c.233-18060=	XM_047444093.1:c.233-18072_233-18060del	XM_047444093.1:c.233-18071_233-18060del	XM_047444093.1:c.233-18064_233-18060del	XM_047444093.1:c.233-18063_233-18060del	XM_047444093.1:c.233-18062_233-18060del	XM_047444093.1:c.233-18061_233-18060del	XM_047444093.1:c.233-18060del	XM_047444093.1:c.233-18060dup	XM_047444093.1:c.233-18061_233-18060dup	XM_047444093.1:c.233-18062_233-18060dup	XM_047444093.1:c.233-18063_233-18060dup	XM_047444093.1:c.233-18064_233-18060dup	XM_047444093.1:c.233-18065_233-18060dup	XM_047444093.1:c.233-18066_233-18060dup	XM_047444093.1:c.233-18067_233-18060dup
NIBAN1 transcript variant X3	XM_047444094.1:c.233-18060=	XM_047444094.1:c.233-18072_233-18060del	XM_047444094.1:c.233-18071_233-18060del	XM_047444094.1:c.233-18064_233-18060del	XM_047444094.1:c.233-18063_233-18060del	XM_047444094.1:c.233-18062_233-18060del	XM_047444094.1:c.233-18061_233-18060del	XM_047444094.1:c.233-18060del	XM_047444094.1:c.233-18060dup	XM_047444094.1:c.233-18061_233-18060dup	XM_047444094.1:c.233-18062_233-18060dup	XM_047444094.1:c.233-18063_233-18060dup	XM_047444094.1:c.233-18064_233-18060dup	XM_047444094.1:c.233-18065_233-18060dup	XM_047444094.1:c.233-18066_233-18060dup	XM_047444094.1:c.233-18067_233-18060dup
NIBAN1 transcript variant X4	XM_047444098.1:c.56-18060=	XM_047444098.1:c.56-18072_56-18060del	XM_047444098.1:c.56-18071_56-18060del	XM_047444098.1:c.56-18064_56-18060del	XM_047444098.1:c.56-18063_56-18060del	XM_047444098.1:c.56-18062_56-18060del	XM_047444098.1:c.56-18061_56-18060del	XM_047444098.1:c.56-18060del	XM_047444098.1:c.56-18060dup	XM_047444098.1:c.56-18061_56-18060dup	XM_047444098.1:c.56-18062_56-18060dup	XM_047444098.1:c.56-18063_56-18060dup	XM_047444098.1:c.56-18064_56-18060dup	XM_047444098.1:c.56-18065_56-18060dup	XM_047444098.1:c.56-18066_56-18060dup	XM_047444098.1:c.56-18067_56-18060dup
NIBAN1 transcript variant X5	XM_047444102.1:c.56-18060=	XM_047444102.1:c.56-18072_56-18060del	XM_047444102.1:c.56-18071_56-18060del	XM_047444102.1:c.56-18064_56-18060del	XM_047444102.1:c.56-18063_56-18060del	XM_047444102.1:c.56-18062_56-18060del	XM_047444102.1:c.56-18061_56-18060del	XM_047444102.1:c.56-18060del	XM_047444102.1:c.56-18060dup	XM_047444102.1:c.56-18061_56-18060dup	XM_047444102.1:c.56-18062_56-18060dup	XM_047444102.1:c.56-18063_56-18060dup	XM_047444102.1:c.56-18064_56-18060dup	XM_047444102.1:c.56-18065_56-18060dup	XM_047444102.1:c.56-18066_56-18060dup	XM_047444102.1:c.56-18067_56-18060dup

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, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80820573	Oct 11, 2018 (152)
2	SWEGEN	ss2988087959	Jan 10, 2018 (151)
3	MCHAISSO	ss3064433776	Nov 08, 2017 (151)
4	URBANLAB	ss3646836638	Oct 11, 2018 (152)
5	PACBIO	ss3794120775	Jul 12, 2019 (153)
6	GNOMAD	ss4007345567	Apr 25, 2021 (155)
7	GNOMAD	ss4007345568	Apr 25, 2021 (155)
8	GNOMAD	ss4007345569	Apr 25, 2021 (155)
9	GNOMAD	ss4007345570	Apr 25, 2021 (155)
10	GNOMAD	ss4007345571	Apr 25, 2021 (155)
11	GNOMAD	ss4007345572	Apr 25, 2021 (155)
12	GNOMAD	ss4007345573	Apr 25, 2021 (155)
13	GNOMAD	ss4007345574	Apr 25, 2021 (155)
14	GNOMAD	ss4007345576	Apr 25, 2021 (155)
15	GNOMAD	ss4007345577	Apr 25, 2021 (155)
16	GNOMAD	ss4007345578	Apr 25, 2021 (155)
17	GNOMAD	ss4007345579	Apr 25, 2021 (155)
18	GNOMAD	ss4007345580	Apr 25, 2021 (155)
19	GNOMAD	ss4007345581	Apr 25, 2021 (155)
20	TOMMO_GENOMICS	ss5147424546	Apr 25, 2021 (155)
21	TOMMO_GENOMICS	ss5147424547	Apr 25, 2021 (155)
22	TOMMO_GENOMICS	ss5147424548	Apr 25, 2021 (155)
23	TOMMO_GENOMICS	ss5147424549	Apr 25, 2021 (155)
24	TOMMO_GENOMICS	ss5147424550	Apr 25, 2021 (155)
25	TOMMO_GENOMICS	ss5147424551	Apr 25, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5245017212	Oct 12, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5245017213	Oct 12, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5245017214	Oct 12, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5245017215	Oct 12, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5245017216	Oct 12, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5245017217	Oct 12, 2022 (156)
32	HUGCELL_USP	ss5445530353	Oct 12, 2022 (156)
33	HUGCELL_USP	ss5445530354	Oct 12, 2022 (156)
34	HUGCELL_USP	ss5445530355	Oct 12, 2022 (156)
35	TOMMO_GENOMICS	ss5674895392	Oct 12, 2022 (156)
36	TOMMO_GENOMICS	ss5674895393	Oct 12, 2022 (156)
37	TOMMO_GENOMICS	ss5674895394	Oct 12, 2022 (156)
38	TOMMO_GENOMICS	ss5674895395	Oct 12, 2022 (156)
39	TOMMO_GENOMICS	ss5674895396	Oct 12, 2022 (156)
40	TOMMO_GENOMICS	ss5674895397	Oct 12, 2022 (156)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 33081428 (NC_000001.11:184917368::T 23881/81210) Row 33081429 (NC_000001.11:184917368::TT 929/81258) Row 33081430 (NC_000001.11:184917368::TTT 124/81278)...	-	Apr 25, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 5393853 (NC_000001.10:184886501:T: 5099/16284) Row 5393854 (NC_000001.10:184886501::T 4170/16284) Row 5393855 (NC_000001.10:184886501::TT 1099/16284)...	-	Apr 25, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 5393853 (NC_000001.10:184886501:T: 5099/16284) Row 5393854 (NC_000001.10:184886501::T 4170/16284) Row 5393855 (NC_000001.10:184886501::TT 1099/16284)...	-	Apr 25, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 5393853 (NC_000001.10:184886501:T: 5099/16284) Row 5393854 (NC_000001.10:184886501::T 4170/16284) Row 5393855 (NC_000001.10:184886501::TT 1099/16284)...	-	Apr 25, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 5393853 (NC_000001.10:184886501:T: 5099/16284) Row 5393854 (NC_000001.10:184886501::T 4170/16284) Row 5393855 (NC_000001.10:184886501::TT 1099/16284)...	-	Apr 25, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 5393853 (NC_000001.10:184886501:T: 5099/16284) Row 5393854 (NC_000001.10:184886501::T 4170/16284) Row 5393855 (NC_000001.10:184886501::TT 1099/16284)...	-	Apr 25, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 5393853 (NC_000001.10:184886501:T: 5099/16284) Row 5393854 (NC_000001.10:184886501::T 4170/16284) Row 5393855 (NC_000001.10:184886501::TT 1099/16284)...	-	Apr 25, 2021 (155)
62	14KJPN Submission ignored due to conflicting rows: Row 8732496 (NC_000001.11:184917368:T: 7231/23568) Row 8732497 (NC_000001.11:184917368::T 5474/23568) Row 8732498 (NC_000001.11:184917368::TT 1395/23568)...	-	Oct 12, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 8732496 (NC_000001.11:184917368:T: 7231/23568) Row 8732497 (NC_000001.11:184917368::T 5474/23568) Row 8732498 (NC_000001.11:184917368::TT 1395/23568)...	-	Oct 12, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 8732496 (NC_000001.11:184917368:T: 7231/23568) Row 8732497 (NC_000001.11:184917368::T 5474/23568) Row 8732498 (NC_000001.11:184917368::TT 1395/23568)...	-	Oct 12, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 8732496 (NC_000001.11:184917368:T: 7231/23568) Row 8732497 (NC_000001.11:184917368::T 5474/23568) Row 8732498 (NC_000001.11:184917368::TT 1395/23568)...	-	Oct 12, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 8732496 (NC_000001.11:184917368:T: 7231/23568) Row 8732497 (NC_000001.11:184917368::T 5474/23568) Row 8732498 (NC_000001.11:184917368::TT 1395/23568)...	-	Oct 12, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 8732496 (NC_000001.11:184917368:T: 7231/23568) Row 8732497 (NC_000001.11:184917368::T 5474/23568) Row 8732498 (NC_000001.11:184917368::TT 1395/23568)...	-	Oct 12, 2022 (156)
68	ALFA	NC_000001.11 - 184917369	Apr 25, 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
ss4007345581	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTT:	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4007345580	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTT:	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4007345579	NC_000001.11:184917368:TTTTT:	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4007345578	NC_000001.11:184917368:TTTT:	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4007345577	NC_000001.11:184917368:TTT:	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss2988087959, ss5147424550	NC_000001.10:184886501:TT:	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007345576, ss5245017214, ss5445530354, ss5674895396	NC_000001.11:184917368:TT:	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3794120775, ss5147424546	NC_000001.10:184886501:T:	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3646836638, ss5245017212, ss5445530353, ss5674895392	NC_000001.11:184917368:T:	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5147424547	NC_000001.10:184886501::T	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3064433776, ss4007345567, ss5245017213, ss5445530355, ss5674895393	NC_000001.11:184917368::T	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss80820573	NT_004487.19:36375168::T	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5147424548	NC_000001.10:184886501::TT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007345568, ss5245017215, ss5674895394	NC_000001.11:184917368::TT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5147424549	NC_000001.10:184886501::TTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007345569, ss5245017216, ss5674895395	NC_000001.11:184917368::TTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5147424551	NC_000001.10:184886501::TTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007345570, ss5674895397	NC_000001.11:184917368::TTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007345571, ss5245017217	NC_000001.11:184917368::TTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007345572	NC_000001.11:184917368::TTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007345573	NC_000001.11:184917368::TTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4007345574	NC_000001.11:184917368::TTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12332531756	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:184917368:TTTTTTTTTTT… NC_000001.11:184917368:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs1168037153

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

rs1168037153