Name: rs11443697
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.

rs11443697

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:101319642-101319661 (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)₉ / del(T)₇ / del(T)₆ / del(…
del(T)₉ / del(T)₇ / del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.0950 (704/7412, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IFT22 : 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	7412	TTTTTTTTTTTTTTTTTTTT=0.8539	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0468, TTTTTTTTTTTTTTTTTTTTT=0.0950, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0015, TTTTTTTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0013, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.856248	0.039964	0.103788	32
European	Sub	6874	TTTTTTTTTTTTTTTTTTTT=0.8424	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0006, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0505, TTTTTTTTTTTTTTTTTTTTT=0.1024, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0016, TTTTTTTTTTTTTTTTTTTTTT=0.0010, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0015, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.843709	0.04345	0.11284	32
African	Sub	246	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	12	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	234	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	16	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	12	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	32	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	122	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	28	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	94	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	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	7412	(T)₂₀=0.8539	del(T)₉=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0005, delTT=0.0000, delT=0.0468, dupT=0.0950, dupTT=0.0009, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0015, dup(T)₆=0.0013
Allele Frequency Aggregator	European	Sub	6874	(T)₂₀=0.8424	del(T)₉=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0006, delTT=0.0000, delT=0.0505, dupT=0.1024, dupTT=0.0010, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0016, dup(T)₆=0.0015
Allele Frequency Aggregator	African	Sub	246	(T)₂₀=1.000	del(T)₉=0.000, del(T)₆=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
Allele Frequency Aggregator	Latin American 2	Sub	122	(T)₂₀=1.000	del(T)₉=0.000, del(T)₆=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
Allele Frequency Aggregator	Other	Sub	94	(T)₂₀=1.00	del(T)₉=0.00, del(T)₆=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
Allele Frequency Aggregator	Latin American 1	Sub	32	(T)₂₀=1.00	del(T)₉=0.00, del(T)₆=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
Allele Frequency Aggregator	South Asian	Sub	28	(T)₂₀=1.00	del(T)₉=0.00, del(T)₆=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
Allele Frequency Aggregator	Asian	Sub	16	(T)₂₀=1.00	del(T)₉=0.00, del(T)₆=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

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 7	NC_000007.14:g.101319653_101319661del
GRCh38.p14 chr 7	NC_000007.14:g.101319655_101319661del
GRCh38.p14 chr 7	NC_000007.14:g.101319656_101319661del
GRCh38.p14 chr 7	NC_000007.14:g.101319658_101319661del
GRCh38.p14 chr 7	NC_000007.14:g.101319659_101319661del
GRCh38.p14 chr 7	NC_000007.14:g.101319660_101319661del
GRCh38.p14 chr 7	NC_000007.14:g.101319661del
GRCh38.p14 chr 7	NC_000007.14:g.101319661dup
GRCh38.p14 chr 7	NC_000007.14:g.101319660_101319661dup
GRCh38.p14 chr 7	NC_000007.14:g.101319659_101319661dup
GRCh38.p14 chr 7	NC_000007.14:g.101319658_101319661dup
GRCh38.p14 chr 7	NC_000007.14:g.101319657_101319661dup
GRCh38.p14 chr 7	NC_000007.14:g.101319656_101319661dup
GRCh38.p14 chr 7	NC_000007.14:g.101319655_101319661dup
GRCh37.p13 chr 7	NC_000007.13:g.100962934_100962942del
GRCh37.p13 chr 7	NC_000007.13:g.100962936_100962942del
GRCh37.p13 chr 7	NC_000007.13:g.100962937_100962942del
GRCh37.p13 chr 7	NC_000007.13:g.100962939_100962942del
GRCh37.p13 chr 7	NC_000007.13:g.100962940_100962942del
GRCh37.p13 chr 7	NC_000007.13:g.100962941_100962942del
GRCh37.p13 chr 7	NC_000007.13:g.100962942del
GRCh37.p13 chr 7	NC_000007.13:g.100962942dup
GRCh37.p13 chr 7	NC_000007.13:g.100962941_100962942dup
GRCh37.p13 chr 7	NC_000007.13:g.100962940_100962942dup
GRCh37.p13 chr 7	NC_000007.13:g.100962939_100962942dup
GRCh37.p13 chr 7	NC_000007.13:g.100962938_100962942dup
GRCh37.p13 chr 7	NC_000007.13:g.100962937_100962942dup
GRCh37.p13 chr 7	NC_000007.13:g.100962936_100962942dup

Gene: IFT22, intraflagellar transport 22 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IFT22 transcript variant 2	NM_001130820.3:c.40-618_4… NM_001130820.3:c.40-618_40-610del	N/A	Intron Variant
IFT22 transcript variant 3	NM_001130821.3:c.-223-587… NM_001130821.3:c.-223-587_-223-579del	N/A	Intron Variant
IFT22 transcript variant 4	NM_001130822.3:c.-115-143… NM_001130822.3:c.-115-1437_-115-1429del	N/A	Intron Variant
IFT22 transcript variant 5	NM_001287525.2:c.-192-618… NM_001287525.2:c.-192-618_-192-610del	N/A	Intron Variant
IFT22 transcript variant 6	NM_001287526.1:c.-26+2021… NM_001287526.1:c.-26+2021_-26+2029del	N/A	Intron Variant
IFT22 transcript variant 1	NM_022777.4:c.40-618_40-6… NM_022777.4:c.40-618_40-610del	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)₂₀=	del(T)₉	del(T)₇	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇
GRCh38.p14 chr 7	NC_000007.14:g.101319642_101319661=	NC_000007.14:g.101319653_101319661del	NC_000007.14:g.101319655_101319661del	NC_000007.14:g.101319656_101319661del	NC_000007.14:g.101319658_101319661del	NC_000007.14:g.101319659_101319661del	NC_000007.14:g.101319660_101319661del	NC_000007.14:g.101319661del	NC_000007.14:g.101319661dup	NC_000007.14:g.101319660_101319661dup	NC_000007.14:g.101319659_101319661dup	NC_000007.14:g.101319658_101319661dup	NC_000007.14:g.101319657_101319661dup	NC_000007.14:g.101319656_101319661dup	NC_000007.14:g.101319655_101319661dup
GRCh37.p13 chr 7	NC_000007.13:g.100962923_100962942=	NC_000007.13:g.100962934_100962942del	NC_000007.13:g.100962936_100962942del	NC_000007.13:g.100962937_100962942del	NC_000007.13:g.100962939_100962942del	NC_000007.13:g.100962940_100962942del	NC_000007.13:g.100962941_100962942del	NC_000007.13:g.100962942del	NC_000007.13:g.100962942dup	NC_000007.13:g.100962941_100962942dup	NC_000007.13:g.100962940_100962942dup	NC_000007.13:g.100962939_100962942dup	NC_000007.13:g.100962938_100962942dup	NC_000007.13:g.100962937_100962942dup	NC_000007.13:g.100962936_100962942dup
RABL5 transcript variant 2	NM_001130820.1:c.40-610=	NM_001130820.1:c.40-618_40-610del	NM_001130820.1:c.40-616_40-610del	NM_001130820.1:c.40-615_40-610del	NM_001130820.1:c.40-613_40-610del	NM_001130820.1:c.40-612_40-610del	NM_001130820.1:c.40-611_40-610del	NM_001130820.1:c.40-610del	NM_001130820.1:c.40-610dup	NM_001130820.1:c.40-611_40-610dup	NM_001130820.1:c.40-612_40-610dup	NM_001130820.1:c.40-613_40-610dup	NM_001130820.1:c.40-614_40-610dup	NM_001130820.1:c.40-615_40-610dup	NM_001130820.1:c.40-616_40-610dup
IFT22 transcript variant 2	NM_001130820.3:c.40-610=	NM_001130820.3:c.40-618_40-610del	NM_001130820.3:c.40-616_40-610del	NM_001130820.3:c.40-615_40-610del	NM_001130820.3:c.40-613_40-610del	NM_001130820.3:c.40-612_40-610del	NM_001130820.3:c.40-611_40-610del	NM_001130820.3:c.40-610del	NM_001130820.3:c.40-610dup	NM_001130820.3:c.40-611_40-610dup	NM_001130820.3:c.40-612_40-610dup	NM_001130820.3:c.40-613_40-610dup	NM_001130820.3:c.40-614_40-610dup	NM_001130820.3:c.40-615_40-610dup	NM_001130820.3:c.40-616_40-610dup
RABL5 transcript variant 3	NM_001130821.1:c.-223-579=	NM_001130821.1:c.-223-587_-223-579del	NM_001130821.1:c.-223-585_-223-579del	NM_001130821.1:c.-223-584_-223-579del	NM_001130821.1:c.-223-582_-223-579del	NM_001130821.1:c.-223-581_-223-579del	NM_001130821.1:c.-223-580_-223-579del	NM_001130821.1:c.-223-579del	NM_001130821.1:c.-223-579dup	NM_001130821.1:c.-223-580_-223-579dup	NM_001130821.1:c.-223-581_-223-579dup	NM_001130821.1:c.-223-582_-223-579dup	NM_001130821.1:c.-223-583_-223-579dup	NM_001130821.1:c.-223-584_-223-579dup	NM_001130821.1:c.-223-585_-223-579dup
IFT22 transcript variant 3	NM_001130821.3:c.-223-579=	NM_001130821.3:c.-223-587_-223-579del	NM_001130821.3:c.-223-585_-223-579del	NM_001130821.3:c.-223-584_-223-579del	NM_001130821.3:c.-223-582_-223-579del	NM_001130821.3:c.-223-581_-223-579del	NM_001130821.3:c.-223-580_-223-579del	NM_001130821.3:c.-223-579del	NM_001130821.3:c.-223-579dup	NM_001130821.3:c.-223-580_-223-579dup	NM_001130821.3:c.-223-581_-223-579dup	NM_001130821.3:c.-223-582_-223-579dup	NM_001130821.3:c.-223-583_-223-579dup	NM_001130821.3:c.-223-584_-223-579dup	NM_001130821.3:c.-223-585_-223-579dup
RABL5 transcript variant 4	NM_001130822.1:c.-115-1429=	NM_001130822.1:c.-115-1437_-115-1429del	NM_001130822.1:c.-115-1435_-115-1429del	NM_001130822.1:c.-115-1434_-115-1429del	NM_001130822.1:c.-115-1432_-115-1429del	NM_001130822.1:c.-115-1431_-115-1429del	NM_001130822.1:c.-115-1430_-115-1429del	NM_001130822.1:c.-115-1429del	NM_001130822.1:c.-115-1429dup	NM_001130822.1:c.-115-1430_-115-1429dup	NM_001130822.1:c.-115-1431_-115-1429dup	NM_001130822.1:c.-115-1432_-115-1429dup	NM_001130822.1:c.-115-1433_-115-1429dup	NM_001130822.1:c.-115-1434_-115-1429dup	NM_001130822.1:c.-115-1435_-115-1429dup
IFT22 transcript variant 4	NM_001130822.3:c.-115-1429=	NM_001130822.3:c.-115-1437_-115-1429del	NM_001130822.3:c.-115-1435_-115-1429del	NM_001130822.3:c.-115-1434_-115-1429del	NM_001130822.3:c.-115-1432_-115-1429del	NM_001130822.3:c.-115-1431_-115-1429del	NM_001130822.3:c.-115-1430_-115-1429del	NM_001130822.3:c.-115-1429del	NM_001130822.3:c.-115-1429dup	NM_001130822.3:c.-115-1430_-115-1429dup	NM_001130822.3:c.-115-1431_-115-1429dup	NM_001130822.3:c.-115-1432_-115-1429dup	NM_001130822.3:c.-115-1433_-115-1429dup	NM_001130822.3:c.-115-1434_-115-1429dup	NM_001130822.3:c.-115-1435_-115-1429dup
IFT22 transcript variant 5	NM_001287525.2:c.-192-610=	NM_001287525.2:c.-192-618_-192-610del	NM_001287525.2:c.-192-616_-192-610del	NM_001287525.2:c.-192-615_-192-610del	NM_001287525.2:c.-192-613_-192-610del	NM_001287525.2:c.-192-612_-192-610del	NM_001287525.2:c.-192-611_-192-610del	NM_001287525.2:c.-192-610del	NM_001287525.2:c.-192-610dup	NM_001287525.2:c.-192-611_-192-610dup	NM_001287525.2:c.-192-612_-192-610dup	NM_001287525.2:c.-192-613_-192-610dup	NM_001287525.2:c.-192-614_-192-610dup	NM_001287525.2:c.-192-615_-192-610dup	NM_001287525.2:c.-192-616_-192-610dup
IFT22 transcript variant 6	NM_001287526.1:c.-26+2029=	NM_001287526.1:c.-26+2021_-26+2029del	NM_001287526.1:c.-26+2023_-26+2029del	NM_001287526.1:c.-26+2024_-26+2029del	NM_001287526.1:c.-26+2026_-26+2029del	NM_001287526.1:c.-26+2027_-26+2029del	NM_001287526.1:c.-26+2028_-26+2029del	NM_001287526.1:c.-26+2029del	NM_001287526.1:c.-26+2029dup	NM_001287526.1:c.-26+2028_-26+2029dup	NM_001287526.1:c.-26+2027_-26+2029dup	NM_001287526.1:c.-26+2026_-26+2029dup	NM_001287526.1:c.-26+2025_-26+2029dup	NM_001287526.1:c.-26+2024_-26+2029dup	NM_001287526.1:c.-26+2023_-26+2029dup
RABL5 transcript variant 1	NM_022777.2:c.40-610=	NM_022777.2:c.40-618_40-610del	NM_022777.2:c.40-616_40-610del	NM_022777.2:c.40-615_40-610del	NM_022777.2:c.40-613_40-610del	NM_022777.2:c.40-612_40-610del	NM_022777.2:c.40-611_40-610del	NM_022777.2:c.40-610del	NM_022777.2:c.40-610dup	NM_022777.2:c.40-611_40-610dup	NM_022777.2:c.40-612_40-610dup	NM_022777.2:c.40-613_40-610dup	NM_022777.2:c.40-614_40-610dup	NM_022777.2:c.40-615_40-610dup	NM_022777.2:c.40-616_40-610dup
IFT22 transcript variant 1	NM_022777.4:c.40-610=	NM_022777.4:c.40-618_40-610del	NM_022777.4:c.40-616_40-610del	NM_022777.4:c.40-615_40-610del	NM_022777.4:c.40-613_40-610del	NM_022777.4:c.40-612_40-610del	NM_022777.4:c.40-611_40-610del	NM_022777.4:c.40-610del	NM_022777.4:c.40-610dup	NM_022777.4:c.40-611_40-610dup	NM_022777.4:c.40-612_40-610dup	NM_022777.4:c.40-613_40-610dup	NM_022777.4:c.40-614_40-610dup	NM_022777.4:c.40-615_40-610dup	NM_022777.4:c.40-616_40-610dup

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#.

44 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42943633	Mar 14, 2006 (144)
2	ABI	ss43104058	Dec 03, 2013 (138)
3	HGSV	ss81113732	Dec 14, 2007 (137)
4	HUMANGENOME_JCVI	ss95469853	Dec 05, 2013 (138)
5	PJP	ss295348701	May 09, 2011 (144)
6	PJP	ss295348702	Jan 10, 2018 (151)
7	SSIP	ss947202670	Aug 21, 2014 (142)
8	EVA_UK10K_ALSPAC	ss1705753937	Jan 10, 2018 (151)
9	EVA_UK10K_TWINSUK	ss1705753970	Jan 10, 2018 (151)
10	EVA_UK10K_ALSPAC	ss1710340523	Oct 12, 2018 (152)
11	EVA_UK10K_TWINSUK	ss1710343954	Oct 12, 2018 (152)
12	SWEGEN	ss3001729481	Nov 08, 2017 (151)
13	EVA	ss3830727457	Apr 26, 2020 (154)
14	GNOMAD	ss4169611136	Apr 26, 2021 (155)
15	GNOMAD	ss4169611137	Apr 26, 2021 (155)
16	GNOMAD	ss4169611138	Apr 26, 2021 (155)
17	GNOMAD	ss4169611139	Apr 26, 2021 (155)
18	GNOMAD	ss4169611140	Apr 26, 2021 (155)
19	GNOMAD	ss4169611141	Apr 26, 2021 (155)
20	GNOMAD	ss4169611142	Apr 26, 2021 (155)
21	GNOMAD	ss4169611143	Apr 26, 2021 (155)
22	GNOMAD	ss4169611144	Apr 26, 2021 (155)
23	GNOMAD	ss4169611145	Apr 26, 2021 (155)
24	GNOMAD	ss4169611146	Apr 26, 2021 (155)
25	GNOMAD	ss4169611147	Apr 26, 2021 (155)
26	GNOMAD	ss4169611148	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5184722862	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5184722863	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5184722864	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5184722865	Apr 26, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5274074671	Oct 13, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5274074672	Oct 13, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5274074673	Oct 13, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5274074674	Oct 13, 2022 (156)
35	HUGCELL_USP	ss5471037650	Oct 13, 2022 (156)
36	HUGCELL_USP	ss5471037651	Oct 13, 2022 (156)
37	HUGCELL_USP	ss5471037652	Oct 13, 2022 (156)
38	HUGCELL_USP	ss5471037653	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5471037654	Oct 13, 2022 (156)
40	TOMMO_GENOMICS	ss5725460343	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5725460344	Oct 13, 2022 (156)
42	TOMMO_GENOMICS	ss5725460345	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5725460346	Oct 13, 2022 (156)
44	EVA	ss5823271672	Oct 13, 2022 (156)
45	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 21364160 (NC_000007.13:100962922:TT: 908/3854) Row 21364161 (NC_000007.13:100962922::T 1870/3854)	-	Oct 12, 2018 (152)
46	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 21364160 (NC_000007.13:100962922:TT: 908/3854) Row 21364161 (NC_000007.13:100962922::T 1870/3854)	-	Oct 12, 2018 (152)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270998209 (NC_000007.14:101319641::T 36264/103102) Row 270998210 (NC_000007.14:101319641::TT 1163/103032) Row 270998211 (NC_000007.14:101319641::TTT 137/103074)...	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 42692169 (NC_000007.13:100962922::T 7238/16314) Row 42692170 (NC_000007.13:100962922::TT 1376/16314) Row 42692171 (NC_000007.13:100962922:T: 8/16314)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 42692169 (NC_000007.13:100962922::T 7238/16314) Row 42692170 (NC_000007.13:100962922::TT 1376/16314) Row 42692171 (NC_000007.13:100962922:T: 8/16314)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 42692169 (NC_000007.13:100962922::T 7238/16314) Row 42692170 (NC_000007.13:100962922::TT 1376/16314) Row 42692171 (NC_000007.13:100962922:T: 8/16314)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 42692169 (NC_000007.13:100962922::T 7238/16314) Row 42692170 (NC_000007.13:100962922::TT 1376/16314) Row 42692171 (NC_000007.13:100962922:T: 8/16314)...	-	Apr 26, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 59297447 (NC_000007.14:101319641::T 13395/28152) Row 59297448 (NC_000007.14:101319641::TT 2515/28152) Row 59297449 (NC_000007.14:101319641:T: 10/28152)...	-	Oct 13, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 59297447 (NC_000007.14:101319641::T 13395/28152) Row 59297448 (NC_000007.14:101319641::TT 2515/28152) Row 59297449 (NC_000007.14:101319641:T: 10/28152)...	-	Oct 13, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 59297447 (NC_000007.14:101319641::T 13395/28152) Row 59297448 (NC_000007.14:101319641::TT 2515/28152) Row 59297449 (NC_000007.14:101319641:T: 10/28152)...	-	Oct 13, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 59297447 (NC_000007.14:101319641::T 13395/28152) Row 59297448 (NC_000007.14:101319641::TT 2515/28152) Row 59297449 (NC_000007.14:101319641:T: 10/28152)...	-	Oct 13, 2022 (156)
69	UK 10K study - Twins Submission ignored due to conflicting rows: Row 21364160 (NC_000007.13:100962922:TT: 827/3708) Row 21364161 (NC_000007.13:100962922::T 1785/3708)	-	Oct 12, 2018 (152)
70	UK 10K study - Twins Submission ignored due to conflicting rows: Row 21364160 (NC_000007.13:100962922:TT: 827/3708) Row 21364161 (NC_000007.13:100962922::T 1785/3708)	-	Oct 12, 2018 (152)
71	ALFA	NC_000007.14 - 101319642	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).

Associated ID	History Updated (Build)
rs11449822	May 11, 2012 (137)
rs34024913	May 11, 2012 (137)
rs34871563	Jul 01, 2015 (144)
rs35756649	May 23, 2006 (127)
rs56933925	May 11, 2012 (137)
rs66964984	May 11, 2012 (137)
rs66964985	Feb 26, 2009 (130)
rs71126402	May 11, 2012 (137)
rs796732113	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4169611148	NC_000007.14:101319641:TTTTTTTTT:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4169611147	NC_000007.14:101319641:TTTTTTT:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4169611146	NC_000007.14:101319641:TTTTTT:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4169611145	NC_000007.14:101319641:TTTT:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3001729481	NC_000007.13:100962922:TTT:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4169611144, ss5471037654	NC_000007.14:101319641:TTT:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss1705753937, ss1705753970, ss5823271672	NC_000007.13:100962922:TT:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4169611143, ss5471037653	NC_000007.14:101319641:TT:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss295348701	NC_000007.12:100749642:T:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5184722864	NC_000007.13:100962922:T:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5274074672, ss5471037650, ss5725460345	NC_000007.14:101319641:T:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss42943633	NT_007933.15:38995765:T:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss95469853	NT_007933.15:38995784:T:	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss295348702	NC_000007.12:100749662::T	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3830727457, ss5184722862	NC_000007.13:100962922::T	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss947202670	NC_000007.13:100962923::T	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss1710340523, ss1710343954	NC_000007.13:100962924::T	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4169611136, ss5274074671, ss5471037651, ss5725460343	NC_000007.14:101319641::T	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss43104058	NT_007933.15:38995766::T	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss81113732	NT_007933.15:38995785::T	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5184722863	NC_000007.13:100962922::TT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169611137, ss5274074673, ss5471037652, ss5725460344	NC_000007.14:101319641::TT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5184722865	NC_000007.13:100962922::TTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169611138, ss5274074674, ss5725460346	NC_000007.14:101319641::TTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169611139	NC_000007.14:101319641::TTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169611140	NC_000007.14:101319641::TTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169611141	NC_000007.14:101319641::TTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9340915793	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4169611142	NC_000007.14:101319641::TTTTTTT	NC_000007.14:101319641:TTTTTTTTTTT… NC_000007.14:101319641:TTTTTTTTTTTTTTTTTTTT: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 rs11443697

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

rs11443697