Name: rs34351733
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.

rs34351733

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:33281407-33281441 (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(GT)₈ / del(GT)₇ / del(GT)₆ / d…
del(GT)₈ / del(GT)₇ / del(GT)₆ / del(GT)₅ / del(GT)₄ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅ / dup(GT)₆ / dup(GT)₇ / dup(GT)₈ / dup(GT)₉ / dup(GT)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupGT=0.0527 (523/9917, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: STARD13 : Intron Variant
STARD13-AS : 500B Downstream 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	9917	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.8837	TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0303, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0314, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0017, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0527, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0002, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.908795	0.008609	0.082597	32
European	Sub	8467	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.8642	TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0352, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0366, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0020, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0618, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0002, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.89038	0.010347	0.099273	27
African	Sub	870	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	30	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	840	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	32	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	28	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	68	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	218	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	48	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other	Sub	214	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.986	TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.009, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.005, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9917	(TG)₁₇T=0.8837	del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0303, delGT=0.0314, dupGT=0.0527, dupGTGT=0.0017, dup(GT)₃=0.0000, dup(GT)₄=0.0002, dup(GT)₅=0.0000, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000, dup(GT)₁₀=0.0000
Allele Frequency Aggregator	European	Sub	8467	(TG)₁₇T=0.8642	del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0352, delGT=0.0366, dupGT=0.0618, dupGTGT=0.0020, dup(GT)₃=0.0000, dup(GT)₄=0.0002, dup(GT)₅=0.0000, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000, dup(GT)₁₀=0.0000
Allele Frequency Aggregator	African	Sub	870	(TG)₁₇T=1.000	del(GT)₈=0.000, del(GT)₇=0.000, del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₉=0.000, dup(GT)₁₀=0.000
Allele Frequency Aggregator	Latin American 2	Sub	218	(TG)₁₇T=1.000	del(GT)₈=0.000, del(GT)₇=0.000, del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₉=0.000, dup(GT)₁₀=0.000
Allele Frequency Aggregator	Other	Sub	214	(TG)₁₇T=0.986	del(GT)₈=0.000, del(GT)₇=0.000, del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₄=0.000, del(GT)₃=0.000, delGTGT=0.009, delGT=0.005, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₉=0.000, dup(GT)₁₀=0.000
Allele Frequency Aggregator	Latin American 1	Sub	68	(TG)₁₇T=1.00	del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00
Allele Frequency Aggregator	South Asian	Sub	48	(TG)₁₇T=1.00	del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00
Allele Frequency Aggregator	Asian	Sub	32	(TG)₁₇T=1.00	del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00, dup(GT)₁₀=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[9]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[10]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[11]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[12]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[13]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[14]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[15]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[16]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[18]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[19]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[20]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[21]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[22]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[23]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[24]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[25]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[26]
GRCh38.p14 chr 13	NC_000013.11:g.33281408GT[27]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[9]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[10]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[11]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[12]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[13]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[14]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[15]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[16]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[18]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[19]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[20]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[21]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[22]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[23]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[24]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[25]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[26]
GRCh37.p13 chr 13	NC_000013.10:g.33855545GT[27]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[9]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[10]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[11]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[12]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[13]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[14]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[15]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[16]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[18]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[19]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[20]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[21]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[22]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[23]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[24]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[25]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[26]
STARD13 RefSeqGene	NG_029752.2:g.400396CA[27]

Gene: STARD13, StAR related lipid transfer domain containing 13 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
STARD13 transcript variant 4	NM_001243476.3:c.65-11381… NM_001243476.3:c.65-113818CA[9]	N/A	Intron Variant
STARD13 transcript variant 1	NM_178006.4:c.169+4030CA[… NM_178006.4:c.169+4030CA[9]	N/A	Intron Variant
STARD13 transcript variant 5	NM_001243466.2:c.	N/A	Genic Upstream Transcript Variant
STARD13 transcript variant 6	NM_001243474.2:c.	N/A	Genic Upstream Transcript Variant
STARD13 transcript variant 3	NM_052851.3:c.	N/A	Genic Upstream Transcript Variant
STARD13 transcript variant 2	NM_178007.3:c.	N/A	Genic Upstream Transcript Variant
STARD13 transcript variant X2	XM_017020834.3:c.124+6885… XM_017020834.3:c.124+68850CA[9]	N/A	Intron Variant
STARD13 transcript variant X3	XM_017020835.3:c.65-11381… XM_017020835.3:c.65-113818CA[9]	N/A	Intron Variant
STARD13 transcript variant X2	XM_024449429.2:c.65-11381… XM_024449429.2:c.65-113818CA[9]	N/A	Intron Variant
STARD13 transcript variant X1	XM_047430759.1:c.200-1138… XM_047430759.1:c.200-113818CA[9]	N/A	Intron Variant
STARD13 transcript variant X4	XM_047430760.1:c.65-11381… XM_047430760.1:c.65-113818CA[9]	N/A	Intron Variant

Gene: STARD13-AS, STARD13 antisense RNA (plus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
STARD13-AS transcript	NR_046693.1:n.	N/A	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	(TG)₁₇T=	del(GT)₈	del(GT)₇	del(GT)₆	del(GT)₅	del(GT)₄	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅	dup(GT)₆	dup(GT)₇	dup(GT)₈	dup(GT)₉	dup(GT)₁₀
GRCh38.p14 chr 13	NC_000013.11:g.33281407_33281441=	NC_000013.11:g.33281408GT[9]	NC_000013.11:g.33281408GT[10]	NC_000013.11:g.33281408GT[11]	NC_000013.11:g.33281408GT[12]	NC_000013.11:g.33281408GT[13]	NC_000013.11:g.33281408GT[14]	NC_000013.11:g.33281408GT[15]	NC_000013.11:g.33281408GT[16]	NC_000013.11:g.33281408GT[18]	NC_000013.11:g.33281408GT[19]	NC_000013.11:g.33281408GT[20]	NC_000013.11:g.33281408GT[21]	NC_000013.11:g.33281408GT[22]	NC_000013.11:g.33281408GT[23]	NC_000013.11:g.33281408GT[24]	NC_000013.11:g.33281408GT[25]	NC_000013.11:g.33281408GT[26]	NC_000013.11:g.33281408GT[27]
GRCh37.p13 chr 13	NC_000013.10:g.33855544_33855578=	NC_000013.10:g.33855545GT[9]	NC_000013.10:g.33855545GT[10]	NC_000013.10:g.33855545GT[11]	NC_000013.10:g.33855545GT[12]	NC_000013.10:g.33855545GT[13]	NC_000013.10:g.33855545GT[14]	NC_000013.10:g.33855545GT[15]	NC_000013.10:g.33855545GT[16]	NC_000013.10:g.33855545GT[18]	NC_000013.10:g.33855545GT[19]	NC_000013.10:g.33855545GT[20]	NC_000013.10:g.33855545GT[21]	NC_000013.10:g.33855545GT[22]	NC_000013.10:g.33855545GT[23]	NC_000013.10:g.33855545GT[24]	NC_000013.10:g.33855545GT[25]	NC_000013.10:g.33855545GT[26]	NC_000013.10:g.33855545GT[27]
STARD13 RefSeqGene	NG_029752.2:g.400395_400429=	NG_029752.2:g.400396CA[9]	NG_029752.2:g.400396CA[10]	NG_029752.2:g.400396CA[11]	NG_029752.2:g.400396CA[12]	NG_029752.2:g.400396CA[13]	NG_029752.2:g.400396CA[14]	NG_029752.2:g.400396CA[15]	NG_029752.2:g.400396CA[16]	NG_029752.2:g.400396CA[18]	NG_029752.2:g.400396CA[19]	NG_029752.2:g.400396CA[20]	NG_029752.2:g.400396CA[21]	NG_029752.2:g.400396CA[22]	NG_029752.2:g.400396CA[23]	NG_029752.2:g.400396CA[24]	NG_029752.2:g.400396CA[25]	NG_029752.2:g.400396CA[26]	NG_029752.2:g.400396CA[27]
STARD13 transcript variant 4	NM_001243476.1:c.65-113785=	NM_001243476.1:c.65-113818CA[9]	NM_001243476.1:c.65-113818CA[10]	NM_001243476.1:c.65-113818CA[11]	NM_001243476.1:c.65-113818CA[12]	NM_001243476.1:c.65-113818CA[13]	NM_001243476.1:c.65-113818CA[14]	NM_001243476.1:c.65-113818CA[15]	NM_001243476.1:c.65-113818CA[16]	NM_001243476.1:c.65-113818CA[18]	NM_001243476.1:c.65-113818CA[19]	NM_001243476.1:c.65-113818CA[20]	NM_001243476.1:c.65-113818CA[21]	NM_001243476.1:c.65-113818CA[22]	NM_001243476.1:c.65-113818CA[23]	NM_001243476.1:c.65-113818CA[24]	NM_001243476.1:c.65-113818CA[25]	NM_001243476.1:c.65-113818CA[26]	NM_001243476.1:c.65-113818CA[27]
STARD13 transcript variant 4	NM_001243476.3:c.65-113785=	NM_001243476.3:c.65-113818CA[9]	NM_001243476.3:c.65-113818CA[10]	NM_001243476.3:c.65-113818CA[11]	NM_001243476.3:c.65-113818CA[12]	NM_001243476.3:c.65-113818CA[13]	NM_001243476.3:c.65-113818CA[14]	NM_001243476.3:c.65-113818CA[15]	NM_001243476.3:c.65-113818CA[16]	NM_001243476.3:c.65-113818CA[18]	NM_001243476.3:c.65-113818CA[19]	NM_001243476.3:c.65-113818CA[20]	NM_001243476.3:c.65-113818CA[21]	NM_001243476.3:c.65-113818CA[22]	NM_001243476.3:c.65-113818CA[23]	NM_001243476.3:c.65-113818CA[24]	NM_001243476.3:c.65-113818CA[25]	NM_001243476.3:c.65-113818CA[26]	NM_001243476.3:c.65-113818CA[27]
STARD13 transcript variant 1	NM_178006.3:c.169+4063=	NM_178006.3:c.169+4030CA[9]	NM_178006.3:c.169+4030CA[10]	NM_178006.3:c.169+4030CA[11]	NM_178006.3:c.169+4030CA[12]	NM_178006.3:c.169+4030CA[13]	NM_178006.3:c.169+4030CA[14]	NM_178006.3:c.169+4030CA[15]	NM_178006.3:c.169+4030CA[16]	NM_178006.3:c.169+4030CA[18]	NM_178006.3:c.169+4030CA[19]	NM_178006.3:c.169+4030CA[20]	NM_178006.3:c.169+4030CA[21]	NM_178006.3:c.169+4030CA[22]	NM_178006.3:c.169+4030CA[23]	NM_178006.3:c.169+4030CA[24]	NM_178006.3:c.169+4030CA[25]	NM_178006.3:c.169+4030CA[26]	NM_178006.3:c.169+4030CA[27]
STARD13 transcript variant 1	NM_178006.4:c.169+4063=	NM_178006.4:c.169+4030CA[9]	NM_178006.4:c.169+4030CA[10]	NM_178006.4:c.169+4030CA[11]	NM_178006.4:c.169+4030CA[12]	NM_178006.4:c.169+4030CA[13]	NM_178006.4:c.169+4030CA[14]	NM_178006.4:c.169+4030CA[15]	NM_178006.4:c.169+4030CA[16]	NM_178006.4:c.169+4030CA[18]	NM_178006.4:c.169+4030CA[19]	NM_178006.4:c.169+4030CA[20]	NM_178006.4:c.169+4030CA[21]	NM_178006.4:c.169+4030CA[22]	NM_178006.4:c.169+4030CA[23]	NM_178006.4:c.169+4030CA[24]	NM_178006.4:c.169+4030CA[25]	NM_178006.4:c.169+4030CA[26]	NM_178006.4:c.169+4030CA[27]
STARD13 transcript variant X1	XM_005266586.1:c.124+68883=	XM_005266586.1:c.124+68850CA[9]	XM_005266586.1:c.124+68850CA[10]	XM_005266586.1:c.124+68850CA[11]	XM_005266586.1:c.124+68850CA[12]	XM_005266586.1:c.124+68850CA[13]	XM_005266586.1:c.124+68850CA[14]	XM_005266586.1:c.124+68850CA[15]	XM_005266586.1:c.124+68850CA[16]	XM_005266586.1:c.124+68850CA[18]	XM_005266586.1:c.124+68850CA[19]	XM_005266586.1:c.124+68850CA[20]	XM_005266586.1:c.124+68850CA[21]	XM_005266586.1:c.124+68850CA[22]	XM_005266586.1:c.124+68850CA[23]	XM_005266586.1:c.124+68850CA[24]	XM_005266586.1:c.124+68850CA[25]	XM_005266586.1:c.124+68850CA[26]	XM_005266586.1:c.124+68850CA[27]
STARD13 transcript variant X2	XM_017020834.3:c.124+68883=	XM_017020834.3:c.124+68850CA[9]	XM_017020834.3:c.124+68850CA[10]	XM_017020834.3:c.124+68850CA[11]	XM_017020834.3:c.124+68850CA[12]	XM_017020834.3:c.124+68850CA[13]	XM_017020834.3:c.124+68850CA[14]	XM_017020834.3:c.124+68850CA[15]	XM_017020834.3:c.124+68850CA[16]	XM_017020834.3:c.124+68850CA[18]	XM_017020834.3:c.124+68850CA[19]	XM_017020834.3:c.124+68850CA[20]	XM_017020834.3:c.124+68850CA[21]	XM_017020834.3:c.124+68850CA[22]	XM_017020834.3:c.124+68850CA[23]	XM_017020834.3:c.124+68850CA[24]	XM_017020834.3:c.124+68850CA[25]	XM_017020834.3:c.124+68850CA[26]	XM_017020834.3:c.124+68850CA[27]
STARD13 transcript variant X3	XM_017020835.3:c.65-113785=	XM_017020835.3:c.65-113818CA[9]	XM_017020835.3:c.65-113818CA[10]	XM_017020835.3:c.65-113818CA[11]	XM_017020835.3:c.65-113818CA[12]	XM_017020835.3:c.65-113818CA[13]	XM_017020835.3:c.65-113818CA[14]	XM_017020835.3:c.65-113818CA[15]	XM_017020835.3:c.65-113818CA[16]	XM_017020835.3:c.65-113818CA[18]	XM_017020835.3:c.65-113818CA[19]	XM_017020835.3:c.65-113818CA[20]	XM_017020835.3:c.65-113818CA[21]	XM_017020835.3:c.65-113818CA[22]	XM_017020835.3:c.65-113818CA[23]	XM_017020835.3:c.65-113818CA[24]	XM_017020835.3:c.65-113818CA[25]	XM_017020835.3:c.65-113818CA[26]	XM_017020835.3:c.65-113818CA[27]
STARD13 transcript variant X2	XM_024449429.2:c.65-113785=	XM_024449429.2:c.65-113818CA[9]	XM_024449429.2:c.65-113818CA[10]	XM_024449429.2:c.65-113818CA[11]	XM_024449429.2:c.65-113818CA[12]	XM_024449429.2:c.65-113818CA[13]	XM_024449429.2:c.65-113818CA[14]	XM_024449429.2:c.65-113818CA[15]	XM_024449429.2:c.65-113818CA[16]	XM_024449429.2:c.65-113818CA[18]	XM_024449429.2:c.65-113818CA[19]	XM_024449429.2:c.65-113818CA[20]	XM_024449429.2:c.65-113818CA[21]	XM_024449429.2:c.65-113818CA[22]	XM_024449429.2:c.65-113818CA[23]	XM_024449429.2:c.65-113818CA[24]	XM_024449429.2:c.65-113818CA[25]	XM_024449429.2:c.65-113818CA[26]	XM_024449429.2:c.65-113818CA[27]
STARD13 transcript variant X1	XM_047430759.1:c.200-113785=	XM_047430759.1:c.200-113818CA[9]	XM_047430759.1:c.200-113818CA[10]	XM_047430759.1:c.200-113818CA[11]	XM_047430759.1:c.200-113818CA[12]	XM_047430759.1:c.200-113818CA[13]	XM_047430759.1:c.200-113818CA[14]	XM_047430759.1:c.200-113818CA[15]	XM_047430759.1:c.200-113818CA[16]	XM_047430759.1:c.200-113818CA[18]	XM_047430759.1:c.200-113818CA[19]	XM_047430759.1:c.200-113818CA[20]	XM_047430759.1:c.200-113818CA[21]	XM_047430759.1:c.200-113818CA[22]	XM_047430759.1:c.200-113818CA[23]	XM_047430759.1:c.200-113818CA[24]	XM_047430759.1:c.200-113818CA[25]	XM_047430759.1:c.200-113818CA[26]	XM_047430759.1:c.200-113818CA[27]
STARD13 transcript variant X4	XM_047430760.1:c.65-113785=	XM_047430760.1:c.65-113818CA[9]	XM_047430760.1:c.65-113818CA[10]	XM_047430760.1:c.65-113818CA[11]	XM_047430760.1:c.65-113818CA[12]	XM_047430760.1:c.65-113818CA[13]	XM_047430760.1:c.65-113818CA[14]	XM_047430760.1:c.65-113818CA[15]	XM_047430760.1:c.65-113818CA[16]	XM_047430760.1:c.65-113818CA[18]	XM_047430760.1:c.65-113818CA[19]	XM_047430760.1:c.65-113818CA[20]	XM_047430760.1:c.65-113818CA[21]	XM_047430760.1:c.65-113818CA[22]	XM_047430760.1:c.65-113818CA[23]	XM_047430760.1:c.65-113818CA[24]	XM_047430760.1:c.65-113818CA[25]	XM_047430760.1:c.65-113818CA[26]	XM_047430760.1:c.65-113818CA[27]

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#.

80 SubSNP, 46 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40392231	Mar 13, 2006 (126)
2	HGSV	ss80513373	Oct 12, 2018 (152)
3	HGSV	ss81809981	Oct 12, 2018 (152)
4	HGSV	ss81822007	Oct 12, 2018 (152)
5	HUMANGENOME_JCVI	ss95763441	Feb 04, 2009 (130)
6	GMI	ss289170157	Oct 12, 2018 (152)
7	1000GENOMES	ss327512659	May 09, 2011 (135)
8	LUNTER	ss552280443	Apr 25, 2013 (138)
9	LUNTER	ss553514330	Apr 25, 2013 (138)
10	SSMP	ss664171907	Sep 08, 2015 (146)
11	BILGI_BIOE	ss666594569	Apr 25, 2013 (138)
12	MCHAISSO	ss3063759641	Nov 08, 2017 (151)
13	MCHAISSO	ss3064590715	Nov 08, 2017 (151)
14	MCHAISSO	ss3064590716	Nov 08, 2017 (151)
15	MCHAISSO	ss3065514188	Nov 08, 2017 (151)
16	EVA_DECODE	ss3695059218	Jul 13, 2019 (153)
17	EVA_DECODE	ss3695059219	Jul 13, 2019 (153)
18	EVA_DECODE	ss3695059220	Jul 13, 2019 (153)
19	EVA_DECODE	ss3695059221	Jul 13, 2019 (153)
20	EVA_DECODE	ss3695059222	Jul 13, 2019 (153)
21	EVA_DECODE	ss3695059223	Jul 13, 2019 (153)
22	ACPOP	ss3739642656	Jul 13, 2019 (153)
23	ACPOP	ss3739642657	Jul 13, 2019 (153)
24	ACPOP	ss3739642658	Jul 13, 2019 (153)
25	ACPOP	ss3739642659	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3816649283	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3816649284	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3816649285	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3816649286	Jul 13, 2019 (153)
30	KHV_HUMAN_GENOMES	ss3816649287	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3816649288	Jul 13, 2019 (153)
32	EVA	ss3845805851	Apr 27, 2020 (154)
33	KOGIC	ss3973334323	Apr 27, 2020 (154)
34	KOGIC	ss3973334324	Apr 27, 2020 (154)
35	KOGIC	ss3973334325	Apr 27, 2020 (154)
36	KOGIC	ss3973334326	Apr 27, 2020 (154)
37	KOGIC	ss3973334327	Apr 27, 2020 (154)
38	KOGIC	ss3973334328	Apr 27, 2020 (154)
39	GNOMAD	ss4263826926	Apr 26, 2021 (155)
40	GNOMAD	ss4263826927	Apr 26, 2021 (155)
41	GNOMAD	ss4263826928	Apr 26, 2021 (155)
42	GNOMAD	ss4263826929	Apr 26, 2021 (155)
43	GNOMAD	ss4263826930	Apr 26, 2021 (155)
44	GNOMAD	ss4263826931	Apr 26, 2021 (155)
45	GNOMAD	ss4263826932	Apr 26, 2021 (155)
46	GNOMAD	ss4263826933	Apr 26, 2021 (155)
47	GNOMAD	ss4263826934	Apr 26, 2021 (155)
48	GNOMAD	ss4263826935	Apr 26, 2021 (155)
49	GNOMAD	ss4263826937	Apr 26, 2021 (155)
50	GNOMAD	ss4263826938	Apr 26, 2021 (155)
51	GNOMAD	ss4263826939	Apr 26, 2021 (155)
52	GNOMAD	ss4263826940	Apr 26, 2021 (155)
53	GNOMAD	ss4263826941	Apr 26, 2021 (155)
54	GNOMAD	ss4263826942	Apr 26, 2021 (155)
55	GNOMAD	ss4263826943	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5209467131	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5209467132	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5209467133	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5209467134	Apr 26, 2021 (155)
60	TOMMO_GENOMICS	ss5209467135	Apr 26, 2021 (155)
61	TOMMO_GENOMICS	ss5209467136	Apr 26, 2021 (155)
62	1000G_HIGH_COVERAGE	ss5293325677	Oct 16, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5293325678	Oct 16, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5293325679	Oct 16, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5293325680	Oct 16, 2022 (156)
66	1000G_HIGH_COVERAGE	ss5293325681	Oct 16, 2022 (156)
67	HUGCELL_USP	ss5487730072	Oct 16, 2022 (156)
68	HUGCELL_USP	ss5487730073	Oct 16, 2022 (156)
69	HUGCELL_USP	ss5487730074	Oct 16, 2022 (156)
70	HUGCELL_USP	ss5487730075	Oct 16, 2022 (156)
71	HUGCELL_USP	ss5487730076	Oct 16, 2022 (156)
72	TOMMO_GENOMICS	ss5761192363	Oct 16, 2022 (156)
73	TOMMO_GENOMICS	ss5761192364	Oct 16, 2022 (156)
74	TOMMO_GENOMICS	ss5761192365	Oct 16, 2022 (156)
75	TOMMO_GENOMICS	ss5761192366	Oct 16, 2022 (156)
76	TOMMO_GENOMICS	ss5761192367	Oct 16, 2022 (156)
77	TOMMO_GENOMICS	ss5761192368	Oct 16, 2022 (156)
78	EVA	ss5839313686	Oct 16, 2022 (156)
79	EVA	ss5839313687	Oct 16, 2022 (156)
80	EVA	ss5839313688	Oct 16, 2022 (156)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 427347524 (NC_000013.11:33281406::TG 21584/135070) Row 427347525 (NC_000013.11:33281406::TGTG 4217/135168) Row 427347526 (NC_000013.11:33281406::TGTGTG 1003/135206)...	-	Apr 26, 2021 (155)
98	Korean Genome Project Submission ignored due to conflicting rows: Row 29712324 (NC_000013.11:33281418::TG 337/1832) Row 29712325 (NC_000013.11:33281418::TGTG 52/1832) Row 29712326 (NC_000013.11:33281406:TGTGTGTGTGTG: 18/1832)...	-	Apr 27, 2020 (154)
99	Korean Genome Project Submission ignored due to conflicting rows: Row 29712324 (NC_000013.11:33281418::TG 337/1832) Row 29712325 (NC_000013.11:33281418::TGTG 52/1832) Row 29712326 (NC_000013.11:33281406:TGTGTGTGTGTG: 18/1832)...	-	Apr 27, 2020 (154)
100	Korean Genome Project Submission ignored due to conflicting rows: Row 29712324 (NC_000013.11:33281418::TG 337/1832) Row 29712325 (NC_000013.11:33281418::TGTG 52/1832) Row 29712326 (NC_000013.11:33281406:TGTGTGTGTGTG: 18/1832)...	-	Apr 27, 2020 (154)
101	Korean Genome Project Submission ignored due to conflicting rows: Row 29712324 (NC_000013.11:33281418::TG 337/1832) Row 29712325 (NC_000013.11:33281418::TGTG 52/1832) Row 29712326 (NC_000013.11:33281406:TGTGTGTGTGTG: 18/1832)...	-	Apr 27, 2020 (154)
102	Korean Genome Project Submission ignored due to conflicting rows: Row 29712324 (NC_000013.11:33281418::TG 337/1832) Row 29712325 (NC_000013.11:33281418::TGTG 52/1832) Row 29712326 (NC_000013.11:33281406:TGTGTGTGTGTG: 18/1832)...	-	Apr 27, 2020 (154)
103	Korean Genome Project Submission ignored due to conflicting rows: Row 29712324 (NC_000013.11:33281418::TG 337/1832) Row 29712325 (NC_000013.11:33281418::TGTG 52/1832) Row 29712326 (NC_000013.11:33281406:TGTGTGTGTGTG: 18/1832)...	-	Apr 27, 2020 (154)
104	Northern Sweden Submission ignored due to conflicting rows: Row 12927521 (NC_000013.10:33855543:TG: 23/600) Row 12927522 (NC_000013.10:33855543:TGTG: 44/600) Row 12927523 (NC_000013.10:33855543::TG 73/600)...	-	Jul 13, 2019 (153)
105	Northern Sweden Submission ignored due to conflicting rows: Row 12927521 (NC_000013.10:33855543:TG: 23/600) Row 12927522 (NC_000013.10:33855543:TGTG: 44/600) Row 12927523 (NC_000013.10:33855543::TG 73/600)...	-	Jul 13, 2019 (153)
106	Northern Sweden Submission ignored due to conflicting rows: Row 12927521 (NC_000013.10:33855543:TG: 23/600) Row 12927522 (NC_000013.10:33855543:TGTG: 44/600) Row 12927523 (NC_000013.10:33855543::TG 73/600)...	-	Jul 13, 2019 (153)
107	Northern Sweden Submission ignored due to conflicting rows: Row 12927521 (NC_000013.10:33855543:TG: 23/600) Row 12927522 (NC_000013.10:33855543:TGTG: 44/600) Row 12927523 (NC_000013.10:33855543::TG 73/600)...	-	Jul 13, 2019 (153)
108	8.3KJPN Submission ignored due to conflicting rows: Row 67436438 (NC_000013.10:33855543::TGTGTG 216/16756) Row 67436439 (NC_000013.10:33855543::TG 2935/16756) Row 67436440 (NC_000013.10:33855543:TG: 223/16756)...	-	Apr 26, 2021 (155)
109	8.3KJPN Submission ignored due to conflicting rows: Row 67436438 (NC_000013.10:33855543::TGTGTG 216/16756) Row 67436439 (NC_000013.10:33855543::TG 2935/16756) Row 67436440 (NC_000013.10:33855543:TG: 223/16756)...	-	Apr 26, 2021 (155)
110	8.3KJPN Submission ignored due to conflicting rows: Row 67436438 (NC_000013.10:33855543::TGTGTG 216/16756) Row 67436439 (NC_000013.10:33855543::TG 2935/16756) Row 67436440 (NC_000013.10:33855543:TG: 223/16756)...	-	Apr 26, 2021 (155)
111	8.3KJPN Submission ignored due to conflicting rows: Row 67436438 (NC_000013.10:33855543::TGTGTG 216/16756) Row 67436439 (NC_000013.10:33855543::TG 2935/16756) Row 67436440 (NC_000013.10:33855543:TG: 223/16756)...	-	Apr 26, 2021 (155)
112	8.3KJPN Submission ignored due to conflicting rows: Row 67436438 (NC_000013.10:33855543::TGTGTG 216/16756) Row 67436439 (NC_000013.10:33855543::TG 2935/16756) Row 67436440 (NC_000013.10:33855543:TG: 223/16756)...	-	Apr 26, 2021 (155)
113	8.3KJPN Submission ignored due to conflicting rows: Row 67436438 (NC_000013.10:33855543::TGTGTG 216/16756) Row 67436439 (NC_000013.10:33855543::TG 2935/16756) Row 67436440 (NC_000013.10:33855543:TG: 223/16756)...	-	Apr 26, 2021 (155)
114	14KJPN Submission ignored due to conflicting rows: Row 95029467 (NC_000013.11:33281406::TG 4857/28258) Row 95029468 (NC_000013.11:33281406::TGTGTGTG 843/28258) Row 95029469 (NC_000013.11:33281406::TGTG 688/28258)...	-	Oct 16, 2022 (156)
115	14KJPN Submission ignored due to conflicting rows: Row 95029467 (NC_000013.11:33281406::TG 4857/28258) Row 95029468 (NC_000013.11:33281406::TGTGTGTG 843/28258) Row 95029469 (NC_000013.11:33281406::TGTG 688/28258)...	-	Oct 16, 2022 (156)
116	14KJPN Submission ignored due to conflicting rows: Row 95029467 (NC_000013.11:33281406::TG 4857/28258) Row 95029468 (NC_000013.11:33281406::TGTGTGTG 843/28258) Row 95029469 (NC_000013.11:33281406::TGTG 688/28258)...	-	Oct 16, 2022 (156)
117	14KJPN Submission ignored due to conflicting rows: Row 95029467 (NC_000013.11:33281406::TG 4857/28258) Row 95029468 (NC_000013.11:33281406::TGTGTGTG 843/28258) Row 95029469 (NC_000013.11:33281406::TGTG 688/28258)...	-	Oct 16, 2022 (156)
118	14KJPN Submission ignored due to conflicting rows: Row 95029467 (NC_000013.11:33281406::TG 4857/28258) Row 95029468 (NC_000013.11:33281406::TGTGTGTG 843/28258) Row 95029469 (NC_000013.11:33281406::TGTG 688/28258)...	-	Oct 16, 2022 (156)
119	14KJPN Submission ignored due to conflicting rows: Row 95029467 (NC_000013.11:33281406::TG 4857/28258) Row 95029468 (NC_000013.11:33281406::TGTGTGTG 843/28258) Row 95029469 (NC_000013.11:33281406::TGTG 688/28258)...	-	Oct 16, 2022 (156)
120	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 7467470 (NC_000013.10:33855543:TG: 10/131) Row 7467471 (NC_000013.10:33855543::TGTGTGTG 11/132) Row 7467472 (NC_000013.10:33855543::TGTGTG 5/126)...	-	Jul 13, 2019 (153)
121	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 7467470 (NC_000013.10:33855543:TG: 10/131) Row 7467471 (NC_000013.10:33855543::TGTGTGTG 11/132) Row 7467472 (NC_000013.10:33855543::TGTGTG 5/126)...	-	Jul 13, 2019 (153)
122	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 7467470 (NC_000013.10:33855543:TG: 10/131) Row 7467471 (NC_000013.10:33855543::TGTGTGTG 11/132) Row 7467472 (NC_000013.10:33855543::TGTGTG 5/126)...	-	Jul 13, 2019 (153)
123	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 7467470 (NC_000013.10:33855543:TG: 10/131) Row 7467471 (NC_000013.10:33855543::TGTGTGTG 11/132) Row 7467472 (NC_000013.10:33855543::TGTGTG 5/126)...	-	Jul 13, 2019 (153)
124	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 7467470 (NC_000013.10:33855543:TG: 10/131) Row 7467471 (NC_000013.10:33855543::TGTGTGTG 11/132) Row 7467472 (NC_000013.10:33855543::TGTGTG 5/126)...	-	Jul 13, 2019 (153)
125	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 7467470 (NC_000013.10:33855543:TG: 10/131) Row 7467471 (NC_000013.10:33855543::TGTGTGTG 11/132) Row 7467472 (NC_000013.10:33855543::TGTGTG 5/126)...	-	Jul 13, 2019 (153)
126	ALFA	NC_000013.11 - 33281407	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)
rs139461472	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss4263826943	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss3973334325, ss4263826942	NC_000013.11:33281406:TGTGTGTGTGTG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4263826941	NC_000013.11:33281406:TGTGTGTGTG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4263826940	NC_000013.11:33281406:TGTGTGTG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3695059218, ss4263826939	NC_000013.11:33281406:TGTGTG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3739642657, ss5209467134, ss5839313687	NC_000013.10:33855543:TGTG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3816649286, ss3845805851, ss4263826938, ss5293325677, ss5487730076, ss5761192367	NC_000013.11:33281406:TGTG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3695059219	NC_000013.11:33281408:TGTG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3973334328	NC_000013.11:33281414:TGTG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss664171907, ss3739642656, ss5209467133, ss5839313688	NC_000013.10:33855543:TG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3064590715, ss4263826937, ss5293325680, ss5487730073, ss5761192366	NC_000013.11:33281406:TG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3816649285	NC_000013.11:33281408:TG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3695059220	NC_000013.11:33281410:TG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss327512659, ss552280443, ss553514330	NC_000013.9:32753543::TG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss289170157	NC_000013.9:32753578::GT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss666594569, ss3739642658, ss5209467132, ss5839313686	NC_000013.10:33855543::TG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3063759641, ss3064590716, ss4263826926, ss5293325678, ss5487730074, ss5761192363	NC_000013.11:33281406::TG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3816649287	NC_000013.11:33281410::TG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3695059221	NC_000013.11:33281412::TG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3973334323	NC_000013.11:33281418::TG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss40392231, ss95763441	NT_024524.14:14835543::TG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss80513373	NT_024524.14:14835578::GT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3739642659, ss5209467135	NC_000013.10:33855543::TGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4263826927, ss5293325679, ss5487730072, ss5761192365	NC_000013.11:33281406::TGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3816649284	NC_000013.11:33281410::TGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3695059222	NC_000013.11:33281412::TGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3973334324	NC_000013.11:33281418::TGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss81809981, ss81822007	NT_024524.14:14835578::GTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5209467131	NC_000013.10:33855543::TGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4263826928, ss5761192368	NC_000013.11:33281406::TGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3816649283	NC_000013.11:33281410::TGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3695059223	NC_000013.11:33281412::TGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3973334327	NC_000013.11:33281418::TGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5209467136	NC_000013.10:33855543::TGTGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3065514188, ss4263826929, ss5293325681, ss5487730075, ss5761192364	NC_000013.11:33281406::TGTGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3816649288	NC_000013.11:33281410::TGTGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3973334326	NC_000013.11:33281418::TGTGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4263826930	NC_000013.11:33281406::TGTGTGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4263826931	NC_000013.11:33281406::TGTGTGTGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4263826932	NC_000013.11:33281406::TGTGTGTGTGT… NC_000013.11:33281406::TGTGTGTGTGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4263826933	NC_000013.11:33281406::TGTGTGTGTGT… NC_000013.11:33281406::TGTGTGTGTGTGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4263826934	NC_000013.11:33281406::TGTGTGTGTGT… NC_000013.11:33281406::TGTGTGTGTGTGTGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4263826935	NC_000013.11:33281406::TGTGTGTGTGT… NC_000013.11:33281406::TGTGTGTGTGTGTGTGTGTG	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
10373129386	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3189644486	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTG:	NC_000013.11:33281406:TGTGTGTGTGTG… NC_000013.11:33281406:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT

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

No publications for rs34351733

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34351733