Name: rs3070736
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.

rs3070736

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:64168903-64168919 (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)₇ / del(T)₆ / del(T)₅ / del(…
del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTTT / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / ins(T)₁₈ / ins(T)₁₉ / ins(T)₃₃
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₇=0.000004 (1/264690, TOPMED)
dup(T)₇=0.2324 (1482/6378, ALFA)
(T)₁₇=0.3946 (1976/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TEX2 : 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	6378	TTTTTTTTTTTTTTTTT=0.7248	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0019, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0027, TTTTTTTTTTTTTTTTTTTTTTTT=0.2324, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0013, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0256, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0114	0.688829	0.146473	0.164698	32
European	Sub	5696	TTTTTTTTTTTTTTTTT=0.6926	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0021, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0030, TTTTTTTTTTTTTTTTTTTTTTTT=0.2595, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0014, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0286, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0128	0.649504	0.165141	0.185355	32
African	Sub	534	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	26	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	508	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	8	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	8	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	14	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	40	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	18	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	68	TTTTTTTTTTTTTTTTT=0.94	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.06, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.911765	0.029412	0.058824	5

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
TopMed	Global	Study-wide	264690	(T)₁₇=0.999996	del(T)₇=0.000004
Allele Frequency Aggregator	Total	Global	6378	(T)₁₇=0.7248	del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0019, dup(T)₅=0.0000, dup(T)₆=0.0027, dup(T)₇=0.2324, dup(T)₈=0.0256, dup(T)₉=0.0114, dup(T)₁₀=0.0013
Allele Frequency Aggregator	European	Sub	5696	(T)₁₇=0.6926	del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0021, dup(T)₅=0.0000, dup(T)₆=0.0030, dup(T)₇=0.2595, dup(T)₈=0.0286, dup(T)₉=0.0128, dup(T)₁₀=0.0014
Allele Frequency Aggregator	African	Sub	534	(T)₁₇=1.000	del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000
Allele Frequency Aggregator	Other	Sub	68	(T)₁₇=0.94	del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.06, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00
Allele Frequency Aggregator	Latin American 2	Sub	40	(T)₁₇=1.00	del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(T)₁₇=1.00	del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(T)₁₇=1.00	del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00
Allele Frequency Aggregator	Asian	Sub	8	(T)₁₇=1.0	del(T)₇=0.0, del(T)₅=0.0, del(T)₄=0.0, delTT=0.0, delT=0.0, dupT=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0, dup(T)₈=0.0, dup(T)₉=0.0, dup(T)₁₀=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dup(T)₇=0.6054
1000Genomes	African	Sub	1322	- No frequency provided	dup(T)₇=0.3026
1000Genomes	East Asian	Sub	1008	- No frequency provided	dup(T)₇=0.7976
1000Genomes	Europe	Sub	1006	- No frequency provided	dup(T)₇=0.6829
1000Genomes	South Asian	Sub	978	- No frequency provided	dup(T)₇=0.596
1000Genomes	American	Sub	694	- No frequency provided	dup(T)₇=0.804

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.64168913_64168919del
GRCh38.p14 chr 17	NC_000017.11:g.64168914_64168919del
GRCh38.p14 chr 17	NC_000017.11:g.64168915_64168919del
GRCh38.p14 chr 17	NC_000017.11:g.64168916_64168919del
GRCh38.p14 chr 17	NC_000017.11:g.64168917_64168919del
GRCh38.p14 chr 17	NC_000017.11:g.64168918_64168919del
GRCh38.p14 chr 17	NC_000017.11:g.64168919del
GRCh38.p14 chr 17	NC_000017.11:g.64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168917_64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168915_64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168914_64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168913_64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168912_64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168911_64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168910_64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168909_64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168908_64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168907_64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168906_64168919dup
GRCh38.p14 chr 17	NC_000017.11:g.64168919_64168920insTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 17	NC_000017.11:g.64168919_64168920insTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 17	NC_000017.11:g.64168919_64168920insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.62246273_62246279del
GRCh37.p13 chr 17	NC_000017.10:g.62246274_62246279del
GRCh37.p13 chr 17	NC_000017.10:g.62246275_62246279del
GRCh37.p13 chr 17	NC_000017.10:g.62246276_62246279del
GRCh37.p13 chr 17	NC_000017.10:g.62246277_62246279del
GRCh37.p13 chr 17	NC_000017.10:g.62246278_62246279del
GRCh37.p13 chr 17	NC_000017.10:g.62246279del
GRCh37.p13 chr 17	NC_000017.10:g.62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246277_62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246275_62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246274_62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246273_62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246272_62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246271_62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246270_62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246269_62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246268_62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246267_62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246266_62246279dup
GRCh37.p13 chr 17	NC_000017.10:g.62246279_62246280insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.62246279_62246280insTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.62246279_62246280insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: TEX2, testis expressed 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TEX2 transcript variant 2	NM_001288732.2:c.2671+219… NM_001288732.2:c.2671+2191_2671+2197del	N/A	Intron Variant
TEX2 transcript variant 3	NM_001288733.2:c.2671+219… NM_001288733.2:c.2671+2191_2671+2197del	N/A	Intron Variant
TEX2 transcript variant 1	NM_018469.5:c.2692+2191_2… NM_018469.5:c.2692+2191_2692+2197del	N/A	Intron Variant
TEX2 transcript variant X1	XM_011524998.2:c.2692+219… XM_011524998.2:c.2692+2191_2692+2197del	N/A	Intron Variant
TEX2 transcript variant X2	XM_011524999.2:c.2692+219… XM_011524999.2:c.2692+2191_2692+2197del	N/A	Intron Variant
TEX2 transcript variant X5	XM_011525000.3:c.2692+219… XM_011525000.3:c.2692+2191_2692+2197del	N/A	Intron Variant
TEX2 transcript variant X9	XM_017024846.3:c.2671+219… XM_017024846.3:c.2671+2191_2671+2197del	N/A	Intron Variant
TEX2 transcript variant X3	XM_047436392.1:c.2692+219… XM_047436392.1:c.2692+2191_2692+2197del	N/A	Intron Variant
TEX2 transcript variant X4	XM_047436393.1:c.2692+219… XM_047436393.1:c.2692+2191_2692+2197del	N/A	Intron Variant
TEX2 transcript variant X6	XM_047436394.1:c.2671+219… XM_047436394.1:c.2671+2191_2671+2197del	N/A	Intron Variant
TEX2 transcript variant X7	XM_047436395.1:c.2671+219… XM_047436395.1:c.2671+2191_2671+2197del	N/A	Intron Variant
TEX2 transcript variant X8	XM_047436396.1:c.2671+219… XM_047436396.1:c.2671+2191_2671+2197del	N/A	Intron Variant
TEX2 transcript variant X10	XM_047436397.1:c.2671+219… XM_047436397.1:c.2671+2191_2671+2197del	N/A	Intron Variant
TEX2 transcript variant X11	XM_017024847.3:c.	N/A	Genic Downstream Transcript 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)₁₇=	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTTT	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	ins(T)₁₈	ins(T)₁₉	ins(T)₃₃
GRCh38.p14 chr 17	NC_000017.11:g.64168903_64168919=	NC_000017.11:g.64168913_64168919del	NC_000017.11:g.64168914_64168919del	NC_000017.11:g.64168915_64168919del	NC_000017.11:g.64168916_64168919del	NC_000017.11:g.64168917_64168919del	NC_000017.11:g.64168918_64168919del	NC_000017.11:g.64168919del	NC_000017.11:g.64168919dup	NC_000017.11:g.64168917_64168919dup	NC_000017.11:g.64168915_64168919dup	NC_000017.11:g.64168914_64168919dup	NC_000017.11:g.64168913_64168919dup	NC_000017.11:g.64168912_64168919dup	NC_000017.11:g.64168911_64168919dup	NC_000017.11:g.64168910_64168919dup	NC_000017.11:g.64168909_64168919dup	NC_000017.11:g.64168908_64168919dup	NC_000017.11:g.64168907_64168919dup	NC_000017.11:g.64168906_64168919dup	NC_000017.11:g.64168919_64168920insTTTTTTTTTTTTTTTTTT	NC_000017.11:g.64168919_64168920insTTTTTTTTTTTTTTTTTTT	NC_000017.11:g.64168919_64168920insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.62246263_62246279=	NC_000017.10:g.62246273_62246279del	NC_000017.10:g.62246274_62246279del	NC_000017.10:g.62246275_62246279del	NC_000017.10:g.62246276_62246279del	NC_000017.10:g.62246277_62246279del	NC_000017.10:g.62246278_62246279del	NC_000017.10:g.62246279del	NC_000017.10:g.62246279dup	NC_000017.10:g.62246277_62246279dup	NC_000017.10:g.62246275_62246279dup	NC_000017.10:g.62246274_62246279dup	NC_000017.10:g.62246273_62246279dup	NC_000017.10:g.62246272_62246279dup	NC_000017.10:g.62246271_62246279dup	NC_000017.10:g.62246270_62246279dup	NC_000017.10:g.62246269_62246279dup	NC_000017.10:g.62246268_62246279dup	NC_000017.10:g.62246267_62246279dup	NC_000017.10:g.62246266_62246279dup	NC_000017.10:g.62246279_62246280insTTTTTTTTTTTTTTTTTT	NC_000017.10:g.62246279_62246280insTTTTTTTTTTTTTTTTTTT	NC_000017.10:g.62246279_62246280insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
TEX2 transcript variant 2	NM_001288732.2:c.2671+2197=	NM_001288732.2:c.2671+2191_2671+2197del	NM_001288732.2:c.2671+2192_2671+2197del	NM_001288732.2:c.2671+2193_2671+2197del	NM_001288732.2:c.2671+2194_2671+2197del	NM_001288732.2:c.2671+2195_2671+2197del	NM_001288732.2:c.2671+2196_2671+2197del	NM_001288732.2:c.2671+2197del	NM_001288732.2:c.2671+2197dup	NM_001288732.2:c.2671+2195_2671+2197dup	NM_001288732.2:c.2671+2193_2671+2197dup	NM_001288732.2:c.2671+2192_2671+2197dup	NM_001288732.2:c.2671+2191_2671+2197dup	NM_001288732.2:c.2671+2190_2671+2197dup	NM_001288732.2:c.2671+2189_2671+2197dup	NM_001288732.2:c.2671+2188_2671+2197dup	NM_001288732.2:c.2671+2187_2671+2197dup	NM_001288732.2:c.2671+2186_2671+2197dup	NM_001288732.2:c.2671+2185_2671+2197dup	NM_001288732.2:c.2671+2184_2671+2197dup	NM_001288732.2:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAA	NM_001288732.2:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAA	NM_001288732.2:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant 3	NM_001288733.2:c.2671+2197=	NM_001288733.2:c.2671+2191_2671+2197del	NM_001288733.2:c.2671+2192_2671+2197del	NM_001288733.2:c.2671+2193_2671+2197del	NM_001288733.2:c.2671+2194_2671+2197del	NM_001288733.2:c.2671+2195_2671+2197del	NM_001288733.2:c.2671+2196_2671+2197del	NM_001288733.2:c.2671+2197del	NM_001288733.2:c.2671+2197dup	NM_001288733.2:c.2671+2195_2671+2197dup	NM_001288733.2:c.2671+2193_2671+2197dup	NM_001288733.2:c.2671+2192_2671+2197dup	NM_001288733.2:c.2671+2191_2671+2197dup	NM_001288733.2:c.2671+2190_2671+2197dup	NM_001288733.2:c.2671+2189_2671+2197dup	NM_001288733.2:c.2671+2188_2671+2197dup	NM_001288733.2:c.2671+2187_2671+2197dup	NM_001288733.2:c.2671+2186_2671+2197dup	NM_001288733.2:c.2671+2185_2671+2197dup	NM_001288733.2:c.2671+2184_2671+2197dup	NM_001288733.2:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAA	NM_001288733.2:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAA	NM_001288733.2:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript	NM_018469.3:c.2692+2197=	NM_018469.3:c.2692+2191_2692+2197del	NM_018469.3:c.2692+2192_2692+2197del	NM_018469.3:c.2692+2193_2692+2197del	NM_018469.3:c.2692+2194_2692+2197del	NM_018469.3:c.2692+2195_2692+2197del	NM_018469.3:c.2692+2196_2692+2197del	NM_018469.3:c.2692+2197del	NM_018469.3:c.2692+2197dup	NM_018469.3:c.2692+2195_2692+2197dup	NM_018469.3:c.2692+2193_2692+2197dup	NM_018469.3:c.2692+2192_2692+2197dup	NM_018469.3:c.2692+2191_2692+2197dup	NM_018469.3:c.2692+2190_2692+2197dup	NM_018469.3:c.2692+2189_2692+2197dup	NM_018469.3:c.2692+2188_2692+2197dup	NM_018469.3:c.2692+2187_2692+2197dup	NM_018469.3:c.2692+2186_2692+2197dup	NM_018469.3:c.2692+2185_2692+2197dup	NM_018469.3:c.2692+2184_2692+2197dup	NM_018469.3:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAA	NM_018469.3:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAA	NM_018469.3:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant 1	NM_018469.5:c.2692+2197=	NM_018469.5:c.2692+2191_2692+2197del	NM_018469.5:c.2692+2192_2692+2197del	NM_018469.5:c.2692+2193_2692+2197del	NM_018469.5:c.2692+2194_2692+2197del	NM_018469.5:c.2692+2195_2692+2197del	NM_018469.5:c.2692+2196_2692+2197del	NM_018469.5:c.2692+2197del	NM_018469.5:c.2692+2197dup	NM_018469.5:c.2692+2195_2692+2197dup	NM_018469.5:c.2692+2193_2692+2197dup	NM_018469.5:c.2692+2192_2692+2197dup	NM_018469.5:c.2692+2191_2692+2197dup	NM_018469.5:c.2692+2190_2692+2197dup	NM_018469.5:c.2692+2189_2692+2197dup	NM_018469.5:c.2692+2188_2692+2197dup	NM_018469.5:c.2692+2187_2692+2197dup	NM_018469.5:c.2692+2186_2692+2197dup	NM_018469.5:c.2692+2185_2692+2197dup	NM_018469.5:c.2692+2184_2692+2197dup	NM_018469.5:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAA	NM_018469.5:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAA	NM_018469.5:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X1	XM_005257504.1:c.2692+2197=	XM_005257504.1:c.2692+2191_2692+2197del	XM_005257504.1:c.2692+2192_2692+2197del	XM_005257504.1:c.2692+2193_2692+2197del	XM_005257504.1:c.2692+2194_2692+2197del	XM_005257504.1:c.2692+2195_2692+2197del	XM_005257504.1:c.2692+2196_2692+2197del	XM_005257504.1:c.2692+2197del	XM_005257504.1:c.2692+2197dup	XM_005257504.1:c.2692+2195_2692+2197dup	XM_005257504.1:c.2692+2193_2692+2197dup	XM_005257504.1:c.2692+2192_2692+2197dup	XM_005257504.1:c.2692+2191_2692+2197dup	XM_005257504.1:c.2692+2190_2692+2197dup	XM_005257504.1:c.2692+2189_2692+2197dup	XM_005257504.1:c.2692+2188_2692+2197dup	XM_005257504.1:c.2692+2187_2692+2197dup	XM_005257504.1:c.2692+2186_2692+2197dup	XM_005257504.1:c.2692+2185_2692+2197dup	XM_005257504.1:c.2692+2184_2692+2197dup	XM_005257504.1:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAA	XM_005257504.1:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAA	XM_005257504.1:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X2	XM_005257505.1:c.2671+2197=	XM_005257505.1:c.2671+2191_2671+2197del	XM_005257505.1:c.2671+2192_2671+2197del	XM_005257505.1:c.2671+2193_2671+2197del	XM_005257505.1:c.2671+2194_2671+2197del	XM_005257505.1:c.2671+2195_2671+2197del	XM_005257505.1:c.2671+2196_2671+2197del	XM_005257505.1:c.2671+2197del	XM_005257505.1:c.2671+2197dup	XM_005257505.1:c.2671+2195_2671+2197dup	XM_005257505.1:c.2671+2193_2671+2197dup	XM_005257505.1:c.2671+2192_2671+2197dup	XM_005257505.1:c.2671+2191_2671+2197dup	XM_005257505.1:c.2671+2190_2671+2197dup	XM_005257505.1:c.2671+2189_2671+2197dup	XM_005257505.1:c.2671+2188_2671+2197dup	XM_005257505.1:c.2671+2187_2671+2197dup	XM_005257505.1:c.2671+2186_2671+2197dup	XM_005257505.1:c.2671+2185_2671+2197dup	XM_005257505.1:c.2671+2184_2671+2197dup	XM_005257505.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAA	XM_005257505.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAA	XM_005257505.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X3	XM_005257506.1:c.2671+2197=	XM_005257506.1:c.2671+2191_2671+2197del	XM_005257506.1:c.2671+2192_2671+2197del	XM_005257506.1:c.2671+2193_2671+2197del	XM_005257506.1:c.2671+2194_2671+2197del	XM_005257506.1:c.2671+2195_2671+2197del	XM_005257506.1:c.2671+2196_2671+2197del	XM_005257506.1:c.2671+2197del	XM_005257506.1:c.2671+2197dup	XM_005257506.1:c.2671+2195_2671+2197dup	XM_005257506.1:c.2671+2193_2671+2197dup	XM_005257506.1:c.2671+2192_2671+2197dup	XM_005257506.1:c.2671+2191_2671+2197dup	XM_005257506.1:c.2671+2190_2671+2197dup	XM_005257506.1:c.2671+2189_2671+2197dup	XM_005257506.1:c.2671+2188_2671+2197dup	XM_005257506.1:c.2671+2187_2671+2197dup	XM_005257506.1:c.2671+2186_2671+2197dup	XM_005257506.1:c.2671+2185_2671+2197dup	XM_005257506.1:c.2671+2184_2671+2197dup	XM_005257506.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAA	XM_005257506.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAA	XM_005257506.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X4	XM_005257507.1:c.2671+2197=	XM_005257507.1:c.2671+2191_2671+2197del	XM_005257507.1:c.2671+2192_2671+2197del	XM_005257507.1:c.2671+2193_2671+2197del	XM_005257507.1:c.2671+2194_2671+2197del	XM_005257507.1:c.2671+2195_2671+2197del	XM_005257507.1:c.2671+2196_2671+2197del	XM_005257507.1:c.2671+2197del	XM_005257507.1:c.2671+2197dup	XM_005257507.1:c.2671+2195_2671+2197dup	XM_005257507.1:c.2671+2193_2671+2197dup	XM_005257507.1:c.2671+2192_2671+2197dup	XM_005257507.1:c.2671+2191_2671+2197dup	XM_005257507.1:c.2671+2190_2671+2197dup	XM_005257507.1:c.2671+2189_2671+2197dup	XM_005257507.1:c.2671+2188_2671+2197dup	XM_005257507.1:c.2671+2187_2671+2197dup	XM_005257507.1:c.2671+2186_2671+2197dup	XM_005257507.1:c.2671+2185_2671+2197dup	XM_005257507.1:c.2671+2184_2671+2197dup	XM_005257507.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAA	XM_005257507.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAA	XM_005257507.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X1	XM_011524998.2:c.2692+2197=	XM_011524998.2:c.2692+2191_2692+2197del	XM_011524998.2:c.2692+2192_2692+2197del	XM_011524998.2:c.2692+2193_2692+2197del	XM_011524998.2:c.2692+2194_2692+2197del	XM_011524998.2:c.2692+2195_2692+2197del	XM_011524998.2:c.2692+2196_2692+2197del	XM_011524998.2:c.2692+2197del	XM_011524998.2:c.2692+2197dup	XM_011524998.2:c.2692+2195_2692+2197dup	XM_011524998.2:c.2692+2193_2692+2197dup	XM_011524998.2:c.2692+2192_2692+2197dup	XM_011524998.2:c.2692+2191_2692+2197dup	XM_011524998.2:c.2692+2190_2692+2197dup	XM_011524998.2:c.2692+2189_2692+2197dup	XM_011524998.2:c.2692+2188_2692+2197dup	XM_011524998.2:c.2692+2187_2692+2197dup	XM_011524998.2:c.2692+2186_2692+2197dup	XM_011524998.2:c.2692+2185_2692+2197dup	XM_011524998.2:c.2692+2184_2692+2197dup	XM_011524998.2:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAA	XM_011524998.2:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAA	XM_011524998.2:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X2	XM_011524999.2:c.2692+2197=	XM_011524999.2:c.2692+2191_2692+2197del	XM_011524999.2:c.2692+2192_2692+2197del	XM_011524999.2:c.2692+2193_2692+2197del	XM_011524999.2:c.2692+2194_2692+2197del	XM_011524999.2:c.2692+2195_2692+2197del	XM_011524999.2:c.2692+2196_2692+2197del	XM_011524999.2:c.2692+2197del	XM_011524999.2:c.2692+2197dup	XM_011524999.2:c.2692+2195_2692+2197dup	XM_011524999.2:c.2692+2193_2692+2197dup	XM_011524999.2:c.2692+2192_2692+2197dup	XM_011524999.2:c.2692+2191_2692+2197dup	XM_011524999.2:c.2692+2190_2692+2197dup	XM_011524999.2:c.2692+2189_2692+2197dup	XM_011524999.2:c.2692+2188_2692+2197dup	XM_011524999.2:c.2692+2187_2692+2197dup	XM_011524999.2:c.2692+2186_2692+2197dup	XM_011524999.2:c.2692+2185_2692+2197dup	XM_011524999.2:c.2692+2184_2692+2197dup	XM_011524999.2:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAA	XM_011524999.2:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAA	XM_011524999.2:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X5	XM_011525000.3:c.2692+2197=	XM_011525000.3:c.2692+2191_2692+2197del	XM_011525000.3:c.2692+2192_2692+2197del	XM_011525000.3:c.2692+2193_2692+2197del	XM_011525000.3:c.2692+2194_2692+2197del	XM_011525000.3:c.2692+2195_2692+2197del	XM_011525000.3:c.2692+2196_2692+2197del	XM_011525000.3:c.2692+2197del	XM_011525000.3:c.2692+2197dup	XM_011525000.3:c.2692+2195_2692+2197dup	XM_011525000.3:c.2692+2193_2692+2197dup	XM_011525000.3:c.2692+2192_2692+2197dup	XM_011525000.3:c.2692+2191_2692+2197dup	XM_011525000.3:c.2692+2190_2692+2197dup	XM_011525000.3:c.2692+2189_2692+2197dup	XM_011525000.3:c.2692+2188_2692+2197dup	XM_011525000.3:c.2692+2187_2692+2197dup	XM_011525000.3:c.2692+2186_2692+2197dup	XM_011525000.3:c.2692+2185_2692+2197dup	XM_011525000.3:c.2692+2184_2692+2197dup	XM_011525000.3:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAA	XM_011525000.3:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAA	XM_011525000.3:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X9	XM_017024846.3:c.2671+2197=	XM_017024846.3:c.2671+2191_2671+2197del	XM_017024846.3:c.2671+2192_2671+2197del	XM_017024846.3:c.2671+2193_2671+2197del	XM_017024846.3:c.2671+2194_2671+2197del	XM_017024846.3:c.2671+2195_2671+2197del	XM_017024846.3:c.2671+2196_2671+2197del	XM_017024846.3:c.2671+2197del	XM_017024846.3:c.2671+2197dup	XM_017024846.3:c.2671+2195_2671+2197dup	XM_017024846.3:c.2671+2193_2671+2197dup	XM_017024846.3:c.2671+2192_2671+2197dup	XM_017024846.3:c.2671+2191_2671+2197dup	XM_017024846.3:c.2671+2190_2671+2197dup	XM_017024846.3:c.2671+2189_2671+2197dup	XM_017024846.3:c.2671+2188_2671+2197dup	XM_017024846.3:c.2671+2187_2671+2197dup	XM_017024846.3:c.2671+2186_2671+2197dup	XM_017024846.3:c.2671+2185_2671+2197dup	XM_017024846.3:c.2671+2184_2671+2197dup	XM_017024846.3:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAA	XM_017024846.3:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAA	XM_017024846.3:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X3	XM_047436392.1:c.2692+2197=	XM_047436392.1:c.2692+2191_2692+2197del	XM_047436392.1:c.2692+2192_2692+2197del	XM_047436392.1:c.2692+2193_2692+2197del	XM_047436392.1:c.2692+2194_2692+2197del	XM_047436392.1:c.2692+2195_2692+2197del	XM_047436392.1:c.2692+2196_2692+2197del	XM_047436392.1:c.2692+2197del	XM_047436392.1:c.2692+2197dup	XM_047436392.1:c.2692+2195_2692+2197dup	XM_047436392.1:c.2692+2193_2692+2197dup	XM_047436392.1:c.2692+2192_2692+2197dup	XM_047436392.1:c.2692+2191_2692+2197dup	XM_047436392.1:c.2692+2190_2692+2197dup	XM_047436392.1:c.2692+2189_2692+2197dup	XM_047436392.1:c.2692+2188_2692+2197dup	XM_047436392.1:c.2692+2187_2692+2197dup	XM_047436392.1:c.2692+2186_2692+2197dup	XM_047436392.1:c.2692+2185_2692+2197dup	XM_047436392.1:c.2692+2184_2692+2197dup	XM_047436392.1:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAA	XM_047436392.1:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAA	XM_047436392.1:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X4	XM_047436393.1:c.2692+2197=	XM_047436393.1:c.2692+2191_2692+2197del	XM_047436393.1:c.2692+2192_2692+2197del	XM_047436393.1:c.2692+2193_2692+2197del	XM_047436393.1:c.2692+2194_2692+2197del	XM_047436393.1:c.2692+2195_2692+2197del	XM_047436393.1:c.2692+2196_2692+2197del	XM_047436393.1:c.2692+2197del	XM_047436393.1:c.2692+2197dup	XM_047436393.1:c.2692+2195_2692+2197dup	XM_047436393.1:c.2692+2193_2692+2197dup	XM_047436393.1:c.2692+2192_2692+2197dup	XM_047436393.1:c.2692+2191_2692+2197dup	XM_047436393.1:c.2692+2190_2692+2197dup	XM_047436393.1:c.2692+2189_2692+2197dup	XM_047436393.1:c.2692+2188_2692+2197dup	XM_047436393.1:c.2692+2187_2692+2197dup	XM_047436393.1:c.2692+2186_2692+2197dup	XM_047436393.1:c.2692+2185_2692+2197dup	XM_047436393.1:c.2692+2184_2692+2197dup	XM_047436393.1:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAA	XM_047436393.1:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAA	XM_047436393.1:c.2692+2197_2692+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X6	XM_047436394.1:c.2671+2197=	XM_047436394.1:c.2671+2191_2671+2197del	XM_047436394.1:c.2671+2192_2671+2197del	XM_047436394.1:c.2671+2193_2671+2197del	XM_047436394.1:c.2671+2194_2671+2197del	XM_047436394.1:c.2671+2195_2671+2197del	XM_047436394.1:c.2671+2196_2671+2197del	XM_047436394.1:c.2671+2197del	XM_047436394.1:c.2671+2197dup	XM_047436394.1:c.2671+2195_2671+2197dup	XM_047436394.1:c.2671+2193_2671+2197dup	XM_047436394.1:c.2671+2192_2671+2197dup	XM_047436394.1:c.2671+2191_2671+2197dup	XM_047436394.1:c.2671+2190_2671+2197dup	XM_047436394.1:c.2671+2189_2671+2197dup	XM_047436394.1:c.2671+2188_2671+2197dup	XM_047436394.1:c.2671+2187_2671+2197dup	XM_047436394.1:c.2671+2186_2671+2197dup	XM_047436394.1:c.2671+2185_2671+2197dup	XM_047436394.1:c.2671+2184_2671+2197dup	XM_047436394.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAA	XM_047436394.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAA	XM_047436394.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X7	XM_047436395.1:c.2671+2197=	XM_047436395.1:c.2671+2191_2671+2197del	XM_047436395.1:c.2671+2192_2671+2197del	XM_047436395.1:c.2671+2193_2671+2197del	XM_047436395.1:c.2671+2194_2671+2197del	XM_047436395.1:c.2671+2195_2671+2197del	XM_047436395.1:c.2671+2196_2671+2197del	XM_047436395.1:c.2671+2197del	XM_047436395.1:c.2671+2197dup	XM_047436395.1:c.2671+2195_2671+2197dup	XM_047436395.1:c.2671+2193_2671+2197dup	XM_047436395.1:c.2671+2192_2671+2197dup	XM_047436395.1:c.2671+2191_2671+2197dup	XM_047436395.1:c.2671+2190_2671+2197dup	XM_047436395.1:c.2671+2189_2671+2197dup	XM_047436395.1:c.2671+2188_2671+2197dup	XM_047436395.1:c.2671+2187_2671+2197dup	XM_047436395.1:c.2671+2186_2671+2197dup	XM_047436395.1:c.2671+2185_2671+2197dup	XM_047436395.1:c.2671+2184_2671+2197dup	XM_047436395.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAA	XM_047436395.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAA	XM_047436395.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X8	XM_047436396.1:c.2671+2197=	XM_047436396.1:c.2671+2191_2671+2197del	XM_047436396.1:c.2671+2192_2671+2197del	XM_047436396.1:c.2671+2193_2671+2197del	XM_047436396.1:c.2671+2194_2671+2197del	XM_047436396.1:c.2671+2195_2671+2197del	XM_047436396.1:c.2671+2196_2671+2197del	XM_047436396.1:c.2671+2197del	XM_047436396.1:c.2671+2197dup	XM_047436396.1:c.2671+2195_2671+2197dup	XM_047436396.1:c.2671+2193_2671+2197dup	XM_047436396.1:c.2671+2192_2671+2197dup	XM_047436396.1:c.2671+2191_2671+2197dup	XM_047436396.1:c.2671+2190_2671+2197dup	XM_047436396.1:c.2671+2189_2671+2197dup	XM_047436396.1:c.2671+2188_2671+2197dup	XM_047436396.1:c.2671+2187_2671+2197dup	XM_047436396.1:c.2671+2186_2671+2197dup	XM_047436396.1:c.2671+2185_2671+2197dup	XM_047436396.1:c.2671+2184_2671+2197dup	XM_047436396.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAA	XM_047436396.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAA	XM_047436396.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
TEX2 transcript variant X10	XM_047436397.1:c.2671+2197=	XM_047436397.1:c.2671+2191_2671+2197del	XM_047436397.1:c.2671+2192_2671+2197del	XM_047436397.1:c.2671+2193_2671+2197del	XM_047436397.1:c.2671+2194_2671+2197del	XM_047436397.1:c.2671+2195_2671+2197del	XM_047436397.1:c.2671+2196_2671+2197del	XM_047436397.1:c.2671+2197del	XM_047436397.1:c.2671+2197dup	XM_047436397.1:c.2671+2195_2671+2197dup	XM_047436397.1:c.2671+2193_2671+2197dup	XM_047436397.1:c.2671+2192_2671+2197dup	XM_047436397.1:c.2671+2191_2671+2197dup	XM_047436397.1:c.2671+2190_2671+2197dup	XM_047436397.1:c.2671+2189_2671+2197dup	XM_047436397.1:c.2671+2188_2671+2197dup	XM_047436397.1:c.2671+2187_2671+2197dup	XM_047436397.1:c.2671+2186_2671+2197dup	XM_047436397.1:c.2671+2185_2671+2197dup	XM_047436397.1:c.2671+2184_2671+2197dup	XM_047436397.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAA	XM_047436397.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAA	XM_047436397.1:c.2671+2197_2671+2198insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

62 SubSNP, 36 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss4302113	Jan 05, 2002 (102)
2	HUMANGENOME_JCVI	ss95698465	Feb 06, 2009 (130)
3	1000GENOMES	ss1376823609	Aug 21, 2014 (142)
4	EVA_UK10K_ALSPAC	ss1708816466	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1708816468	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1708816550	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1708816551	Apr 01, 2015 (144)
8	SWEGEN	ss3015772500	Nov 08, 2017 (151)
9	SWEGEN	ss3015772501	Nov 08, 2017 (151)
10	SWEGEN	ss3015772502	Nov 08, 2017 (151)
11	SWEGEN	ss3015772503	Nov 08, 2017 (151)
12	SWEGEN	ss3015772504	Nov 08, 2017 (151)
13	PACBIO	ss3788244772	Jul 13, 2019 (153)
14	PACBIO	ss3793193972	Jul 13, 2019 (153)
15	PACBIO	ss3793193973	Jul 13, 2019 (153)
16	PACBIO	ss3798079792	Jul 13, 2019 (153)
17	PACBIO	ss3798079793	Jul 13, 2019 (153)
18	KHV_HUMAN_GENOMES	ss3820100353	Jul 13, 2019 (153)
19	EVA	ss3834936727	Apr 27, 2020 (154)
20	GNOMAD	ss4314211468	Apr 26, 2021 (155)
21	GNOMAD	ss4314211469	Apr 26, 2021 (155)
22	GNOMAD	ss4314211470	Apr 26, 2021 (155)
23	GNOMAD	ss4314211471	Apr 26, 2021 (155)
24	GNOMAD	ss4314211472	Apr 26, 2021 (155)
25	GNOMAD	ss4314211473	Apr 26, 2021 (155)
26	GNOMAD	ss4314211474	Apr 26, 2021 (155)
27	GNOMAD	ss4314211475	Apr 26, 2021 (155)
28	GNOMAD	ss4314211476	Apr 26, 2021 (155)
29	GNOMAD	ss4314211477	Apr 26, 2021 (155)
30	GNOMAD	ss4314211478	Apr 26, 2021 (155)
31	GNOMAD	ss4314211479	Apr 26, 2021 (155)
32	GNOMAD	ss4314211480	Apr 26, 2021 (155)
33	GNOMAD	ss4314211481	Apr 26, 2021 (155)
34	GNOMAD	ss4314211483	Apr 26, 2021 (155)
35	GNOMAD	ss4314211484	Apr 26, 2021 (155)
36	GNOMAD	ss4314211485	Apr 26, 2021 (155)
37	GNOMAD	ss4314211486	Apr 26, 2021 (155)
38	TOPMED	ss5041109103	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5223105788	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5223105789	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5223105790	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5223105791	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5223105792	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5303646438	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5303646439	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5303646440	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5303646441	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5303646442	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5496637823	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5496637824	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5496637825	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5779530595	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5779530596	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5779530597	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5779530598	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5779530599	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5779530600	Oct 16, 2022 (156)
58	EVA	ss5834177632	Oct 16, 2022 (156)
59	EVA	ss5834177633	Oct 16, 2022 (156)
60	EVA	ss5834177634	Oct 16, 2022 (156)
61	EVA	ss5834177635	Oct 16, 2022 (156)
62	EVA	ss5851861242	Oct 16, 2022 (156)
63	1000Genomes	NC_000017.10 - 62246263	Oct 12, 2018 (152)
64	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 40168665 (NC_000017.10:62246262::TTTTTTT 803/3854) Row 40168666 (NC_000017.10:62246262::TTTTTT 649/3854)	-	Oct 12, 2018 (152)
65	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 40168665 (NC_000017.10:62246262::TTTTTTT 803/3854) Row 40168666 (NC_000017.10:62246262::TTTTTT 649/3854)	-	Oct 12, 2018 (152)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 511564603 (NC_000017.11:64168902::T 249/99336) Row 511564604 (NC_000017.11:64168902::TTTTT 5/99336) Row 511564605 (NC_000017.11:64168902::TTTTTT 1668/99292)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 81075095 (NC_000017.10:62246262::TTTTTTT 9441/15522) Row 81075096 (NC_000017.10:62246262::TTTTTTTT 426/15522) Row 81075097 (NC_000017.10:62246262::TTTTTT 88/15522)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 81075095 (NC_000017.10:62246262::TTTTTTT 9441/15522) Row 81075096 (NC_000017.10:62246262::TTTTTTTT 426/15522) Row 81075097 (NC_000017.10:62246262::TTTTTT 88/15522)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 81075095 (NC_000017.10:62246262::TTTTTTT 9441/15522) Row 81075096 (NC_000017.10:62246262::TTTTTTTT 426/15522) Row 81075097 (NC_000017.10:62246262::TTTTTT 88/15522)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 81075095 (NC_000017.10:62246262::TTTTTTT 9441/15522) Row 81075096 (NC_000017.10:62246262::TTTTTTTT 426/15522) Row 81075097 (NC_000017.10:62246262::TTTTTT 88/15522)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 81075095 (NC_000017.10:62246262::TTTTTTT 9441/15522) Row 81075096 (NC_000017.10:62246262::TTTTTTTT 426/15522) Row 81075097 (NC_000017.10:62246262::TTTTTT 88/15522)...	-	Apr 26, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 113367699 (NC_000017.11:64168902::TTTTTTT 18175/27400) Row 113367700 (NC_000017.11:64168902::TTTTTTTT 780/27400) Row 113367701 (NC_000017.11:64168902::TTTTTT 153/27400)...	-	Oct 16, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 113367699 (NC_000017.11:64168902::TTTTTTT 18175/27400) Row 113367700 (NC_000017.11:64168902::TTTTTTTT 780/27400) Row 113367701 (NC_000017.11:64168902::TTTTTT 153/27400)...	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 113367699 (NC_000017.11:64168902::TTTTTTT 18175/27400) Row 113367700 (NC_000017.11:64168902::TTTTTTTT 780/27400) Row 113367701 (NC_000017.11:64168902::TTTTTT 153/27400)...	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 113367699 (NC_000017.11:64168902::TTTTTTT 18175/27400) Row 113367700 (NC_000017.11:64168902::TTTTTTTT 780/27400) Row 113367701 (NC_000017.11:64168902::TTTTTT 153/27400)...	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 113367699 (NC_000017.11:64168902::TTTTTTT 18175/27400) Row 113367700 (NC_000017.11:64168902::TTTTTTTT 780/27400) Row 113367701 (NC_000017.11:64168902::TTTTTT 153/27400)...	-	Oct 16, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 113367699 (NC_000017.11:64168902::TTTTTTT 18175/27400) Row 113367700 (NC_000017.11:64168902::TTTTTTTT 780/27400) Row 113367701 (NC_000017.11:64168902::TTTTTT 153/27400)...	-	Oct 16, 2022 (156)
95	TopMed	NC_000017.11 - 64168903	Apr 26, 2021 (155)
96	UK 10K study - Twins Submission ignored due to conflicting rows: Row 40168665 (NC_000017.10:62246262::TTTTTTT 752/3708) Row 40168666 (NC_000017.10:62246262::TTTTTT 620/3708)	-	Oct 12, 2018 (152)
97	UK 10K study - Twins Submission ignored due to conflicting rows: Row 40168665 (NC_000017.10:62246262::TTTTTTT 752/3708) Row 40168666 (NC_000017.10:62246262::TTTTTT 620/3708)	-	Oct 12, 2018 (152)
98	ALFA	NC_000017.11 - 64168903	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)
rs66643038	Feb 26, 2009 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
256654765, ss5041109103	NC_000017.11:64168902:TTTTTTT:	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss5779530599	NC_000017.11:64168902:TTTTTT:	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4314211486	NC_000017.11:64168902:TTTT:	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4314211485	NC_000017.11:64168902:TTT:	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4314211484	NC_000017.11:64168902:TT:	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4314211483	NC_000017.11:64168902:T:	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3015772502, ss5223105792	NC_000017.10:62246262::T	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4314211468, ss5303646442, ss5779530600	NC_000017.11:64168902::T	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5834177635	NC_000017.10:62246262::TTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
ss5834177634	NC_000017.10:62246262::TTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
ss4314211469	NC_000017.11:64168902::TTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss1708816468, ss1708816551, ss3015772500, ss3793193972, ss3798079792, ss5223105790, ss5834177633	NC_000017.10:62246262::TTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4314211470, ss5303646441, ss5496637824, ss5779530597	NC_000017.11:64168902::TTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
72490901, ss1376823609, ss1708816466, ss1708816550, ss3015772501, ss3788244772, ss3793193973, ss3798079793, ss5223105788, ss5834177632	NC_000017.10:62246262::TTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3820100353, ss4314211471, ss5303646438, ss5496637823, ss5779530595	NC_000017.11:64168902::TTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4302113, ss95698465	NT_010783.15:27520431::TTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3015772504, ss3834936727, ss5223105789	NC_000017.10:62246262::TTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4314211472, ss5303646440, ss5496637825, ss5779530596, ss5851861242	NC_000017.11:64168902::TTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3015772503, ss5223105791	NC_000017.10:62246262::TTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4314211473, ss5303646439, ss5779530598	NC_000017.11:64168902::TTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4314211474	NC_000017.11:64168902::TTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8027658683	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4314211475	NC_000017.11:64168902::TTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4314211476	NC_000017.11:64168902::TTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4314211477	NC_000017.11:64168902::TTTTTTTTTTT… NC_000017.11:64168902::TTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4314211478	NC_000017.11:64168902::TTTTTTTTTTT… NC_000017.11:64168902::TTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4314211479	NC_000017.11:64168902::TTTTTTTTTTT… NC_000017.11:64168902::TTTTTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4314211480	NC_000017.11:64168902::TTTTTTTTTTT… NC_000017.11:64168902::TTTTTTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4314211481	NC_000017.11:64168902::TTTTTTTTTTT… NC_000017.11:64168902::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:64168902:TTTTTTTTTTTT… NC_000017.11:64168902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs3070736

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

rs3070736