Name: rs71361745
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.

rs71361745

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:54959617-54959634 (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)₅ / del(T)₄ / delTTT / delTT…
del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₇ / dup(T)₉
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.1871 (1235/6602, ALFA)
delT=0.2837 (1421/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: COX11 : Intron Variant
TOM1L1 : 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	6602	TTTTTTTTTTTTTTTTTT=0.6593	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTTT=0.1506, TTTTTTTTTTTTTTTTTTTT=0.1871, TTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTT=0.0024, TTTTTTTTTTTTTTTTTTTTTT=0.0000	0.700837	0.102092	0.197071	32
European	Sub	5980	TTTTTTTTTTTTTTTTTT=0.6247	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTTT=0.1659, TTTTTTTTTTTTTTTTTTTT=0.2060, TTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTT=0.0027, TTTTTTTTTTTTTTTTTTTTTT=0.0000	0.656896	0.117251	0.225853	32
African	Sub	272	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	2	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	270	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	52	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	44	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	26	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	160	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	22	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	90	TTTTTTTTTTTTTTTTTT=0.94	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	0.976744	0.0	0.023256	0

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	6602	(T)₁₈=0.6593	del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0002, delT=0.1506, dupT=0.0005, dupTT=0.1871, dupTTT=0.0024, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	5980	(T)₁₈=0.6247	del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0002, delT=0.1659, dupT=0.0005, dupTT=0.2060, dupTTT=0.0027, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	272	(T)₁₈=1.000	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
Allele Frequency Aggregator	Latin American 2	Sub	160	(T)₁₈=1.000	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
Allele Frequency Aggregator	Other	Sub	90	(T)₁₈=0.94	del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.02, dupT=0.00, dupTT=0.03, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	52	(T)₁₈=1.00	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
Allele Frequency Aggregator	Latin American 1	Sub	26	(T)₁₈=1.00	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
Allele Frequency Aggregator	South Asian	Sub	22	(T)₁₈=1.00	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
1000Genomes	Global	Study-wide	5008	(T)₁₈=0.7163	delT=0.2837
1000Genomes	African	Sub	1322	(T)₁₈=0.5938	delT=0.4062
1000Genomes	East Asian	Sub	1008	(T)₁₈=0.8095	delT=0.1905
1000Genomes	Europe	Sub	1006	(T)₁₈=0.7048	delT=0.2952
1000Genomes	South Asian	Sub	978	(T)₁₈=0.766	delT=0.234
1000Genomes	American	Sub	694	(T)₁₈=0.761	delT=0.239

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 17	NC_000017.11:g.54959630_54959634del
GRCh38.p14 chr 17	NC_000017.11:g.54959631_54959634del
GRCh38.p14 chr 17	NC_000017.11:g.54959632_54959634del
GRCh38.p14 chr 17	NC_000017.11:g.54959633_54959634del
GRCh38.p14 chr 17	NC_000017.11:g.54959634del
GRCh38.p14 chr 17	NC_000017.11:g.54959634dup
GRCh38.p14 chr 17	NC_000017.11:g.54959633_54959634dup
GRCh38.p14 chr 17	NC_000017.11:g.54959632_54959634dup
GRCh38.p14 chr 17	NC_000017.11:g.54959631_54959634dup
GRCh38.p14 chr 17	NC_000017.11:g.54959630_54959634dup
GRCh38.p14 chr 17	NC_000017.11:g.54959628_54959634dup
GRCh38.p14 chr 17	NC_000017.11:g.54959626_54959634dup
GRCh37.p13 chr 17	NC_000017.10:g.53036991_53036995del
GRCh37.p13 chr 17	NC_000017.10:g.53036992_53036995del
GRCh37.p13 chr 17	NC_000017.10:g.53036993_53036995del
GRCh37.p13 chr 17	NC_000017.10:g.53036994_53036995del
GRCh37.p13 chr 17	NC_000017.10:g.53036995del
GRCh37.p13 chr 17	NC_000017.10:g.53036995dup
GRCh37.p13 chr 17	NC_000017.10:g.53036994_53036995dup
GRCh37.p13 chr 17	NC_000017.10:g.53036993_53036995dup
GRCh37.p13 chr 17	NC_000017.10:g.53036992_53036995dup
GRCh37.p13 chr 17	NC_000017.10:g.53036991_53036995dup
GRCh37.p13 chr 17	NC_000017.10:g.53036989_53036995dup
GRCh37.p13 chr 17	NC_000017.10:g.53036987_53036995dup

Gene: TOM1L1, target of myb1 like 1 membrane trafficking protein (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TOM1L1 transcript variant 3	NM_001321174.2:c.1140-936… NM_001321174.2:c.1140-936_1140-932del	N/A	Intron Variant
TOM1L1 transcript variant 4	NM_001321175.2:c.1140-936… NM_001321175.2:c.1140-936_1140-932del	N/A	Intron Variant
TOM1L1 transcript variant 5	NM_001321176.2:c.1140-936… NM_001321176.2:c.1140-936_1140-932del	N/A	Intron Variant
TOM1L1 transcript variant 1	NM_005486.3:c.1371-936_13… NM_005486.3:c.1371-936_1371-932del	N/A	Intron Variant
TOM1L1 transcript variant 2	NM_001321173.2:c.	N/A	Genic Downstream Transcript Variant
TOM1L1 transcript variant X3	XM_047435068.1:c.1086-936… XM_047435068.1:c.1086-936_1086-932del	N/A	Intron Variant
TOM1L1 transcript variant X4	XM_047435069.1:c.1266-936… XM_047435069.1:c.1266-936_1266-932del	N/A	Intron Variant
TOM1L1 transcript variant X1	XM_047435067.1:c.	N/A	Genic Downstream Transcript Variant
TOM1L1 transcript variant X2	XR_243612.4:n.	N/A	Intron Variant

Gene: COX11, cytochrome c oxidase copper chaperone COX11 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
COX11 transcript variant 2	NM_001162861.2:c.	N/A	Genic Downstream Transcript Variant
COX11 transcript variant 3	NM_001162862.2:c.	N/A	Genic Downstream Transcript Variant
COX11 transcript variant 6	NM_001321518.1:c.	N/A	Genic Downstream Transcript Variant
COX11 transcript variant 1	NM_004375.5:c.	N/A	Genic Downstream Transcript Variant
COX11 transcript variant 4	NR_027941.3:n.	N/A	Intron Variant
COX11 transcript variant 5	NR_027942.3:n.	N/A	Intron Variant
COX11 transcript variant 7	NR_135677.2:n.	N/A	Intron Variant
COX11 transcript variant X1	XM_011524342.4:c.1615-15… XM_011524342.4:c.1615-155_*1615-151del	N/A	Intron Variant
COX11 transcript variant X2	XM_017024192.3:c.1615-15… XM_017024192.3:c.1615-151_*1615-147del	N/A	Intron Variant
COX11 transcript variant X7	XM_017024196.3:c.146+149… XM_017024196.3:c.146+1498_*146+1502del	N/A	Intron Variant
COX11 transcript variant X5	XM_024450583.2:c.147-155… XM_024450583.2:c.147-155_*147-151del	N/A	Intron Variant
COX11 transcript variant X6	XM_024450584.2:c.147-151… XM_024450584.2:c.147-151_*147-147del	N/A	Intron Variant
COX11 transcript variant X3	XM_047435370.1:c.1614+14… XM_047435370.1:c.1614+1498_*1614+1502del	N/A	Intron Variant
COX11 transcript variant X4	XM_047435372.1:c.3099_3… XM_047435372.1:c.3099_3116=	N/A	3 Prime UTR 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)₁₈=	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₇	dup(T)₉
GRCh38.p14 chr 17	NC_000017.11:g.54959617_54959634=	NC_000017.11:g.54959630_54959634del	NC_000017.11:g.54959631_54959634del	NC_000017.11:g.54959632_54959634del	NC_000017.11:g.54959633_54959634del	NC_000017.11:g.54959634del	NC_000017.11:g.54959634dup	NC_000017.11:g.54959633_54959634dup	NC_000017.11:g.54959632_54959634dup	NC_000017.11:g.54959631_54959634dup	NC_000017.11:g.54959630_54959634dup	NC_000017.11:g.54959628_54959634dup	NC_000017.11:g.54959626_54959634dup
GRCh37.p13 chr 17	NC_000017.10:g.53036978_53036995=	NC_000017.10:g.53036991_53036995del	NC_000017.10:g.53036992_53036995del	NC_000017.10:g.53036993_53036995del	NC_000017.10:g.53036994_53036995del	NC_000017.10:g.53036995del	NC_000017.10:g.53036995dup	NC_000017.10:g.53036994_53036995dup	NC_000017.10:g.53036993_53036995dup	NC_000017.10:g.53036992_53036995dup	NC_000017.10:g.53036991_53036995dup	NC_000017.10:g.53036989_53036995dup	NC_000017.10:g.53036987_53036995dup
COX11 transcript variant X4	XM_047435372.1:c.3099_3116=	XM_047435372.1:c.3112_3116del	XM_047435372.1:c.3113_3116del	XM_047435372.1:c.3114_3116del	XM_047435372.1:c.3115_3116del	XM_047435372.1:c.*3116del	XM_047435372.1:c.*3116dup	XM_047435372.1:c.3115_3116dup	XM_047435372.1:c.3114_3116dup	XM_047435372.1:c.3113_3116dup	XM_047435372.1:c.3112_3116dup	XM_047435372.1:c.3110_3116dup	XM_047435372.1:c.3108_3116dup
TOM1L1 transcript variant 3	NM_001321174.2:c.1140-949=	NM_001321174.2:c.1140-936_1140-932del	NM_001321174.2:c.1140-935_1140-932del	NM_001321174.2:c.1140-934_1140-932del	NM_001321174.2:c.1140-933_1140-932del	NM_001321174.2:c.1140-932del	NM_001321174.2:c.1140-932dup	NM_001321174.2:c.1140-933_1140-932dup	NM_001321174.2:c.1140-934_1140-932dup	NM_001321174.2:c.1140-935_1140-932dup	NM_001321174.2:c.1140-936_1140-932dup	NM_001321174.2:c.1140-938_1140-932dup	NM_001321174.2:c.1140-940_1140-932dup
TOM1L1 transcript variant 4	NM_001321175.2:c.1140-949=	NM_001321175.2:c.1140-936_1140-932del	NM_001321175.2:c.1140-935_1140-932del	NM_001321175.2:c.1140-934_1140-932del	NM_001321175.2:c.1140-933_1140-932del	NM_001321175.2:c.1140-932del	NM_001321175.2:c.1140-932dup	NM_001321175.2:c.1140-933_1140-932dup	NM_001321175.2:c.1140-934_1140-932dup	NM_001321175.2:c.1140-935_1140-932dup	NM_001321175.2:c.1140-936_1140-932dup	NM_001321175.2:c.1140-938_1140-932dup	NM_001321175.2:c.1140-940_1140-932dup
TOM1L1 transcript variant 5	NM_001321176.2:c.1140-949=	NM_001321176.2:c.1140-936_1140-932del	NM_001321176.2:c.1140-935_1140-932del	NM_001321176.2:c.1140-934_1140-932del	NM_001321176.2:c.1140-933_1140-932del	NM_001321176.2:c.1140-932del	NM_001321176.2:c.1140-932dup	NM_001321176.2:c.1140-933_1140-932dup	NM_001321176.2:c.1140-934_1140-932dup	NM_001321176.2:c.1140-935_1140-932dup	NM_001321176.2:c.1140-936_1140-932dup	NM_001321176.2:c.1140-938_1140-932dup	NM_001321176.2:c.1140-940_1140-932dup
TOM1L1 transcript variant 1	NM_005486.2:c.1371-949=	NM_005486.2:c.1371-936_1371-932del	NM_005486.2:c.1371-935_1371-932del	NM_005486.2:c.1371-934_1371-932del	NM_005486.2:c.1371-933_1371-932del	NM_005486.2:c.1371-932del	NM_005486.2:c.1371-932dup	NM_005486.2:c.1371-933_1371-932dup	NM_005486.2:c.1371-934_1371-932dup	NM_005486.2:c.1371-935_1371-932dup	NM_005486.2:c.1371-936_1371-932dup	NM_005486.2:c.1371-938_1371-932dup	NM_005486.2:c.1371-940_1371-932dup
TOM1L1 transcript variant 1	NM_005486.3:c.1371-949=	NM_005486.3:c.1371-936_1371-932del	NM_005486.3:c.1371-935_1371-932del	NM_005486.3:c.1371-934_1371-932del	NM_005486.3:c.1371-933_1371-932del	NM_005486.3:c.1371-932del	NM_005486.3:c.1371-932dup	NM_005486.3:c.1371-933_1371-932dup	NM_005486.3:c.1371-934_1371-932dup	NM_005486.3:c.1371-935_1371-932dup	NM_005486.3:c.1371-936_1371-932dup	NM_005486.3:c.1371-938_1371-932dup	NM_005486.3:c.1371-940_1371-932dup
TOM1L1 transcript variant X1	XM_005256913.1:c.1350-949=	XM_005256913.1:c.1350-936_1350-932del	XM_005256913.1:c.1350-935_1350-932del	XM_005256913.1:c.1350-934_1350-932del	XM_005256913.1:c.1350-933_1350-932del	XM_005256913.1:c.1350-932del	XM_005256913.1:c.1350-932dup	XM_005256913.1:c.1350-933_1350-932dup	XM_005256913.1:c.1350-934_1350-932dup	XM_005256913.1:c.1350-935_1350-932dup	XM_005256913.1:c.1350-936_1350-932dup	XM_005256913.1:c.1350-938_1350-932dup	XM_005256913.1:c.1350-940_1350-932dup
TOM1L1 transcript variant X2	XM_005256914.1:c.1140-949=	XM_005256914.1:c.1140-936_1140-932del	XM_005256914.1:c.1140-935_1140-932del	XM_005256914.1:c.1140-934_1140-932del	XM_005256914.1:c.1140-933_1140-932del	XM_005256914.1:c.1140-932del	XM_005256914.1:c.1140-932dup	XM_005256914.1:c.1140-933_1140-932dup	XM_005256914.1:c.1140-934_1140-932dup	XM_005256914.1:c.1140-935_1140-932dup	XM_005256914.1:c.1140-936_1140-932dup	XM_005256914.1:c.1140-938_1140-932dup	XM_005256914.1:c.1140-940_1140-932dup
TOM1L1 transcript variant X3	XM_005256915.1:c.1140-949=	XM_005256915.1:c.1140-936_1140-932del	XM_005256915.1:c.1140-935_1140-932del	XM_005256915.1:c.1140-934_1140-932del	XM_005256915.1:c.1140-933_1140-932del	XM_005256915.1:c.1140-932del	XM_005256915.1:c.1140-932dup	XM_005256915.1:c.1140-933_1140-932dup	XM_005256915.1:c.1140-934_1140-932dup	XM_005256915.1:c.1140-935_1140-932dup	XM_005256915.1:c.1140-936_1140-932dup	XM_005256915.1:c.1140-938_1140-932dup	XM_005256915.1:c.1140-940_1140-932dup
TOM1L1 transcript variant X4	XM_005256916.1:c.1140-949=	XM_005256916.1:c.1140-936_1140-932del	XM_005256916.1:c.1140-935_1140-932del	XM_005256916.1:c.1140-934_1140-932del	XM_005256916.1:c.1140-933_1140-932del	XM_005256916.1:c.1140-932del	XM_005256916.1:c.1140-932dup	XM_005256916.1:c.1140-933_1140-932dup	XM_005256916.1:c.1140-934_1140-932dup	XM_005256916.1:c.1140-935_1140-932dup	XM_005256916.1:c.1140-936_1140-932dup	XM_005256916.1:c.1140-938_1140-932dup	XM_005256916.1:c.1140-940_1140-932dup
COX11 transcript variant X1	XM_011524342.4:c.*1615-151=	XM_011524342.4:c.1615-155_1615-151del	XM_011524342.4:c.1615-154_1615-151del	XM_011524342.4:c.1615-153_1615-151del	XM_011524342.4:c.1615-152_1615-151del	XM_011524342.4:c.*1615-151del	XM_011524342.4:c.*1615-151dup	XM_011524342.4:c.1615-152_1615-151dup	XM_011524342.4:c.1615-153_1615-151dup	XM_011524342.4:c.1615-154_1615-151dup	XM_011524342.4:c.1615-155_1615-151dup	XM_011524342.4:c.1615-157_1615-151dup	XM_011524342.4:c.1615-159_1615-151dup
COX11 transcript variant X2	XM_017024192.3:c.*1615-147=	XM_017024192.3:c.1615-151_1615-147del	XM_017024192.3:c.1615-150_1615-147del	XM_017024192.3:c.1615-149_1615-147del	XM_017024192.3:c.1615-148_1615-147del	XM_017024192.3:c.*1615-147del	XM_017024192.3:c.*1615-147dup	XM_017024192.3:c.1615-148_1615-147dup	XM_017024192.3:c.1615-149_1615-147dup	XM_017024192.3:c.1615-150_1615-147dup	XM_017024192.3:c.1615-151_1615-147dup	XM_017024192.3:c.1615-153_1615-147dup	XM_017024192.3:c.1615-155_1615-147dup
COX11 transcript variant X7	XM_017024196.3:c.*146+1502=	XM_017024196.3:c.146+1498_146+1502del	XM_017024196.3:c.146+1499_146+1502del	XM_017024196.3:c.146+1500_146+1502del	XM_017024196.3:c.146+1501_146+1502del	XM_017024196.3:c.*146+1502del	XM_017024196.3:c.*146+1502dup	XM_017024196.3:c.146+1501_146+1502dup	XM_017024196.3:c.146+1500_146+1502dup	XM_017024196.3:c.146+1499_146+1502dup	XM_017024196.3:c.146+1498_146+1502dup	XM_017024196.3:c.146+1496_146+1502dup	XM_017024196.3:c.146+1494_146+1502dup
COX11 transcript variant X5	XM_024450583.2:c.*147-151=	XM_024450583.2:c.147-155_147-151del	XM_024450583.2:c.147-154_147-151del	XM_024450583.2:c.147-153_147-151del	XM_024450583.2:c.147-152_147-151del	XM_024450583.2:c.*147-151del	XM_024450583.2:c.*147-151dup	XM_024450583.2:c.147-152_147-151dup	XM_024450583.2:c.147-153_147-151dup	XM_024450583.2:c.147-154_147-151dup	XM_024450583.2:c.147-155_147-151dup	XM_024450583.2:c.147-157_147-151dup	XM_024450583.2:c.147-159_147-151dup
COX11 transcript variant X6	XM_024450584.2:c.*147-147=	XM_024450584.2:c.147-151_147-147del	XM_024450584.2:c.147-150_147-147del	XM_024450584.2:c.147-149_147-147del	XM_024450584.2:c.147-148_147-147del	XM_024450584.2:c.*147-147del	XM_024450584.2:c.*147-147dup	XM_024450584.2:c.147-148_147-147dup	XM_024450584.2:c.147-149_147-147dup	XM_024450584.2:c.147-150_147-147dup	XM_024450584.2:c.147-151_147-147dup	XM_024450584.2:c.147-153_147-147dup	XM_024450584.2:c.147-155_147-147dup
TOM1L1 transcript variant X3	XM_047435068.1:c.1086-949=	XM_047435068.1:c.1086-936_1086-932del	XM_047435068.1:c.1086-935_1086-932del	XM_047435068.1:c.1086-934_1086-932del	XM_047435068.1:c.1086-933_1086-932del	XM_047435068.1:c.1086-932del	XM_047435068.1:c.1086-932dup	XM_047435068.1:c.1086-933_1086-932dup	XM_047435068.1:c.1086-934_1086-932dup	XM_047435068.1:c.1086-935_1086-932dup	XM_047435068.1:c.1086-936_1086-932dup	XM_047435068.1:c.1086-938_1086-932dup	XM_047435068.1:c.1086-940_1086-932dup
TOM1L1 transcript variant X4	XM_047435069.1:c.1266-949=	XM_047435069.1:c.1266-936_1266-932del	XM_047435069.1:c.1266-935_1266-932del	XM_047435069.1:c.1266-934_1266-932del	XM_047435069.1:c.1266-933_1266-932del	XM_047435069.1:c.1266-932del	XM_047435069.1:c.1266-932dup	XM_047435069.1:c.1266-933_1266-932dup	XM_047435069.1:c.1266-934_1266-932dup	XM_047435069.1:c.1266-935_1266-932dup	XM_047435069.1:c.1266-936_1266-932dup	XM_047435069.1:c.1266-938_1266-932dup	XM_047435069.1:c.1266-940_1266-932dup
COX11 transcript variant X3	XM_047435370.1:c.*1614+1502=	XM_047435370.1:c.1614+1498_1614+1502del	XM_047435370.1:c.1614+1499_1614+1502del	XM_047435370.1:c.1614+1500_1614+1502del	XM_047435370.1:c.1614+1501_1614+1502del	XM_047435370.1:c.*1614+1502del	XM_047435370.1:c.*1614+1502dup	XM_047435370.1:c.1614+1501_1614+1502dup	XM_047435370.1:c.1614+1500_1614+1502dup	XM_047435370.1:c.1614+1499_1614+1502dup	XM_047435370.1:c.1614+1498_1614+1502dup	XM_047435370.1:c.1614+1496_1614+1502dup	XM_047435370.1:c.1614+1494_1614+1502dup

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#.

59 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss79838442	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95696752	Oct 12, 2018 (152)
3	HUMANGENOME_JCVI	ss96569294	Mar 15, 2016 (147)
4	GMI	ss289330601	May 04, 2012 (137)
5	PJP	ss294917436	May 09, 2011 (137)
6	1000GENOMES	ss1376758818	Aug 21, 2014 (142)
7	EVA_UK10K_ALSPAC	ss1708792488	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1708792745	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710735987	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710735992	Apr 01, 2015 (144)
11	SWEGEN	ss3015676206	Nov 08, 2017 (151)
12	URBANLAB	ss3650673548	Oct 12, 2018 (152)
13	EVA_DECODE	ss3700634490	Jul 13, 2019 (153)
14	EVA_DECODE	ss3700634491	Jul 13, 2019 (153)
15	EVA_DECODE	ss3700634492	Jul 13, 2019 (153)
16	EVA_DECODE	ss3700634493	Jul 13, 2019 (153)
17	EVA_DECODE	ss3700634494	Jul 13, 2019 (153)
18	EVA_DECODE	ss3700634495	Jul 13, 2019 (153)
19	ACPOP	ss3742098506	Jul 13, 2019 (153)
20	ACPOP	ss3742098507	Jul 13, 2019 (153)
21	KHV_HUMAN_GENOMES	ss3820032722	Jul 13, 2019 (153)
22	EVA	ss3834909833	Apr 27, 2020 (154)
23	GNOMAD	ss4313111945	Apr 27, 2021 (155)
24	GNOMAD	ss4313111946	Apr 27, 2021 (155)
25	GNOMAD	ss4313111947	Apr 27, 2021 (155)
26	GNOMAD	ss4313111948	Apr 27, 2021 (155)
27	GNOMAD	ss4313111949	Apr 27, 2021 (155)
28	GNOMAD	ss4313111950	Apr 27, 2021 (155)
29	GNOMAD	ss4313111951	Apr 27, 2021 (155)
30	GNOMAD	ss4313111952	Apr 27, 2021 (155)
31	GNOMAD	ss4313111953	Apr 27, 2021 (155)
32	GNOMAD	ss4313111954	Apr 27, 2021 (155)
33	GNOMAD	ss4313111955	Apr 27, 2021 (155)
34	TOMMO_GENOMICS	ss5222819360	Apr 27, 2021 (155)
35	TOMMO_GENOMICS	ss5222819361	Apr 27, 2021 (155)
36	TOMMO_GENOMICS	ss5222819362	Apr 27, 2021 (155)
37	TOMMO_GENOMICS	ss5222819363	Apr 27, 2021 (155)
38	TOMMO_GENOMICS	ss5222819364	Apr 27, 2021 (155)
39	TOMMO_GENOMICS	ss5222819365	Apr 27, 2021 (155)
40	1000G_HIGH_COVERAGE	ss5303430396	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5303430397	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5303430398	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5303430399	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5303430400	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5496447040	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5496447041	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5496447042	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5496447043	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5496447044	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5779154888	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5779154889	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5779154890	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5779154891	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5779154892	Oct 16, 2022 (156)
55	EVA	ss5834098666	Oct 16, 2022 (156)
56	EVA	ss5834098667	Oct 16, 2022 (156)
57	EVA	ss5834098668	Oct 16, 2022 (156)
58	EVA	ss5851840090	Oct 16, 2022 (156)
59	EVA	ss5914264864	Oct 16, 2022 (156)
60	1000Genomes	NC_000017.10 - 53036978	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 40030806 (NC_000017.10:53036977:T: 1222/3854) Row 40030807 (NC_000017.10:53036977::TT 1090/3854)	-	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 40030806 (NC_000017.10:53036977:T: 1222/3854) Row 40030807 (NC_000017.10:53036977::TT 1090/3854)	-	Oct 12, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 509737872 (NC_000017.11:54959616::T 2588/127402) Row 509737873 (NC_000017.11:54959616::TT 34544/127252) Row 509737874 (NC_000017.11:54959616::TTT 508/127414)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 509737872 (NC_000017.11:54959616::T 2588/127402) Row 509737873 (NC_000017.11:54959616::TT 34544/127252) Row 509737874 (NC_000017.11:54959616::TTT 508/127414)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 509737872 (NC_000017.11:54959616::T 2588/127402) Row 509737873 (NC_000017.11:54959616::TT 34544/127252) Row 509737874 (NC_000017.11:54959616::TTT 508/127414)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 509737872 (NC_000017.11:54959616::T 2588/127402) Row 509737873 (NC_000017.11:54959616::TT 34544/127252) Row 509737874 (NC_000017.11:54959616::TTT 508/127414)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 509737872 (NC_000017.11:54959616::T 2588/127402) Row 509737873 (NC_000017.11:54959616::TT 34544/127252) Row 509737874 (NC_000017.11:54959616::TTT 508/127414)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 509737872 (NC_000017.11:54959616::T 2588/127402) Row 509737873 (NC_000017.11:54959616::TT 34544/127252) Row 509737874 (NC_000017.11:54959616::TTT 508/127414)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 509737872 (NC_000017.11:54959616::T 2588/127402) Row 509737873 (NC_000017.11:54959616::TT 34544/127252) Row 509737874 (NC_000017.11:54959616::TTT 508/127414)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 509737872 (NC_000017.11:54959616::T 2588/127402) Row 509737873 (NC_000017.11:54959616::TT 34544/127252) Row 509737874 (NC_000017.11:54959616::TTT 508/127414)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 509737872 (NC_000017.11:54959616::T 2588/127402) Row 509737873 (NC_000017.11:54959616::TT 34544/127252) Row 509737874 (NC_000017.11:54959616::TTT 508/127414)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 509737872 (NC_000017.11:54959616::T 2588/127402) Row 509737873 (NC_000017.11:54959616::TT 34544/127252) Row 509737874 (NC_000017.11:54959616::TTT 508/127414)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 509737872 (NC_000017.11:54959616::T 2588/127402) Row 509737873 (NC_000017.11:54959616::TT 34544/127252) Row 509737874 (NC_000017.11:54959616::TTT 508/127414)...	-	Apr 27, 2021 (155)
74	Northern Sweden Submission ignored due to conflicting rows: Row 15383371 (NC_000017.10:53036977:T: 96/600) Row 15383372 (NC_000017.10:53036977::TT 211/600)	-	Jul 13, 2019 (153)
75	Northern Sweden Submission ignored due to conflicting rows: Row 15383371 (NC_000017.10:53036977:T: 96/600) Row 15383372 (NC_000017.10:53036977::TT 211/600)	-	Jul 13, 2019 (153)
76	8.3KJPN Submission ignored due to conflicting rows: Row 80788667 (NC_000017.10:53036977:T: 1162/16758) Row 80788668 (NC_000017.10:53036977::TT 2068/16758) Row 80788669 (NC_000017.10:53036977::T 115/16758)...	-	Apr 27, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 80788667 (NC_000017.10:53036977:T: 1162/16758) Row 80788668 (NC_000017.10:53036977::TT 2068/16758) Row 80788669 (NC_000017.10:53036977::T 115/16758)...	-	Apr 27, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 80788667 (NC_000017.10:53036977:T: 1162/16758) Row 80788668 (NC_000017.10:53036977::TT 2068/16758) Row 80788669 (NC_000017.10:53036977::T 115/16758)...	-	Apr 27, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 80788667 (NC_000017.10:53036977:T: 1162/16758) Row 80788668 (NC_000017.10:53036977::TT 2068/16758) Row 80788669 (NC_000017.10:53036977::T 115/16758)...	-	Apr 27, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 80788667 (NC_000017.10:53036977:T: 1162/16758) Row 80788668 (NC_000017.10:53036977::TT 2068/16758) Row 80788669 (NC_000017.10:53036977::T 115/16758)...	-	Apr 27, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 80788667 (NC_000017.10:53036977:T: 1162/16758) Row 80788668 (NC_000017.10:53036977::TT 2068/16758) Row 80788669 (NC_000017.10:53036977::T 115/16758)...	-	Apr 27, 2021 (155)
82	14KJPN Submission ignored due to conflicting rows: Row 112991992 (NC_000017.11:54959616:T: 1864/28258) Row 112991993 (NC_000017.11:54959616::TT 3612/28258) Row 112991994 (NC_000017.11:54959616::T 177/28258)...	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 112991992 (NC_000017.11:54959616:T: 1864/28258) Row 112991993 (NC_000017.11:54959616::TT 3612/28258) Row 112991994 (NC_000017.11:54959616::T 177/28258)...	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 112991992 (NC_000017.11:54959616:T: 1864/28258) Row 112991993 (NC_000017.11:54959616::TT 3612/28258) Row 112991994 (NC_000017.11:54959616::T 177/28258)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 112991992 (NC_000017.11:54959616:T: 1864/28258) Row 112991993 (NC_000017.11:54959616::TT 3612/28258) Row 112991994 (NC_000017.11:54959616::T 177/28258)...	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 112991992 (NC_000017.11:54959616:T: 1864/28258) Row 112991993 (NC_000017.11:54959616::TT 3612/28258) Row 112991994 (NC_000017.11:54959616::T 177/28258)...	-	Oct 16, 2022 (156)
87	UK 10K study - Twins Submission ignored due to conflicting rows: Row 40030806 (NC_000017.10:53036977:T: 1110/3708) Row 40030807 (NC_000017.10:53036977::TT 1057/3708)	-	Oct 12, 2018 (152)
88	UK 10K study - Twins Submission ignored due to conflicting rows: Row 40030806 (NC_000017.10:53036977:T: 1110/3708) Row 40030807 (NC_000017.10:53036977::TT 1057/3708)	-	Oct 12, 2018 (152)
89	ALFA	NC_000017.11 - 54959617	Apr 27, 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)
rs151037190	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4313111955	NC_000017.11:54959616:TTTTT:	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
12506365154	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4313111954	NC_000017.11:54959616:TTTT:	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
12506365154	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4313111953	NC_000017.11:54959616:TTT:	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12506365154	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5222819364	NC_000017.10:53036977:TT:	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3700634490, ss4313111952, ss5303430400, ss5496447043, ss5779154892	NC_000017.11:54959616:TT:	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12506365154	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss289330601	NC_000017.9:50391976:T:	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss294917436	NC_000017.9:50391993:T:	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
72238929, ss1376758818, ss1708792488, ss1708792745, ss3015676206, ss3742098506, ss5222819360, ss5834098667	NC_000017.10:53036977:T:	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3820032722, ss4313111951, ss5303430398, ss5496447040, ss5779154888	NC_000017.11:54959616:T:	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
12506365154	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3700634491	NC_000017.11:54959617:T:	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss96569294	NT_010783.15:18311129:T:	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5222819362	NC_000017.10:53036977::T	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4313111945, ss5303430397, ss5496447042, ss5779154890, ss5851840090	NC_000017.11:54959616::T	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
12506365154	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3700634492	NC_000017.11:54959618::T	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3742098507, ss3834909833, ss5222819361, ss5834098666	NC_000017.10:53036977::TT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss1710735987, ss1710735992	NC_000017.10:53036978::TT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3650673548, ss4313111946, ss5303430396, ss5496447041, ss5779154889, ss5914264864	NC_000017.11:54959616::TT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
12506365154	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3700634493	NC_000017.11:54959618::TT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss96569294	NT_010783.15:18311129:T:TTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss79838442, ss95696752	NT_010783.15:18311147::TT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5222819363, ss5834098668	NC_000017.10:53036977::TTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4313111947, ss5303430399, ss5496447044, ss5779154891	NC_000017.11:54959616::TTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
12506365154	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3700634494	NC_000017.11:54959618::TTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5222819365	NC_000017.10:53036977::TTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4313111948	NC_000017.11:54959616::TTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
12506365154	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4313111949	NC_000017.11:54959616::TTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4313111950	NC_000017.11:54959616::TTTTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3700634495	NC_000017.11:54959618::TTTTTTTTT	NC_000017.11:54959616:TTTTTTTTTTTT… NC_000017.11:54959616:TTTTTTTTTTTTTTTTTT: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 rs71361745

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs71361745