Name: rs778467789
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.

rs778467789

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:40730521-40730539 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₃ / del(T)₁₂ / del(T)₁₀ / d…
del(T)₁₃ / del(T)₁₂ / del(T)₁₀ / del(T)₉ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / insC(T)₂₄ / insC(T)₃₉ / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₁₈ / dup(T)₁₉ / ins(T)₂₀ / ins(T)₂₁ / ins(T)₂₂
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.02098 (324/15446, ALFA)
(T)₁₉=0.05 (2/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RAD51 : 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	15446	TTTTTTTTTTTTTTTTTTT=0.97605	TTTTTT=0.00000, TTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00013, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.02098, TTTTTTTTTTTTTTTTTTTT=0.00285, TTTTTTTTTTTTTTTTTTTTT=0.00000	0.963272	0.004949	0.031779	32
European	Sub	12882	TTTTTTTTTTTTTTTTTTT=0.97128	TTTTTT=0.00000, TTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00016, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.02515, TTTTTTTTTTTTTTTTTTTT=0.00342, TTTTTTTTTTTTTTTTTTTTT=0.00000	0.95591	0.005941	0.038149	32
African	Sub	1436	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	56	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1380	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	72	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	60	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	110	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	502	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	88	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	356	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=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	15446	(T)₁₉=0.97605	del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₀=0.00000, del(T)₅=0.00013, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.02098, dupT=0.00285, dupTT=0.00000
Allele Frequency Aggregator	European	Sub	12882	(T)₁₉=0.97128	del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₀=0.00000, del(T)₅=0.00016, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.02515, dupT=0.00342, dupTT=0.00000
Allele Frequency Aggregator	African	Sub	1436	(T)₁₉=1.0000	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	502	(T)₁₉=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	356	(T)₁₉=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	110	(T)₁₉=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	South Asian	Sub	88	(T)₁₉=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	72	(T)₁₉=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dup(T)₁₉=0.95

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 15	NC_000015.10:g.40730527_40730539del
GRCh38.p14 chr 15	NC_000015.10:g.40730528_40730539del
GRCh38.p14 chr 15	NC_000015.10:g.40730530_40730539del
GRCh38.p14 chr 15	NC_000015.10:g.40730531_40730539del
GRCh38.p14 chr 15	NC_000015.10:g.40730534_40730539del
GRCh38.p14 chr 15	NC_000015.10:g.40730535_40730539del
GRCh38.p14 chr 15	NC_000015.10:g.40730536_40730539del
GRCh38.p14 chr 15	NC_000015.10:g.40730537_40730539del
GRCh38.p14 chr 15	NC_000015.10:g.40730538_40730539del
GRCh38.p14 chr 15	NC_000015.10:g.40730539del
GRCh38.p14 chr 15	NC_000015.10:g.40730521_40730539T[19]CTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 15	NC_000015.10:g.40730521_40730539T[19]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 15	NC_000015.10:g.40730539dup
GRCh38.p14 chr 15	NC_000015.10:g.40730538_40730539dup
GRCh38.p14 chr 15	NC_000015.10:g.40730537_40730539dup
GRCh38.p14 chr 15	NC_000015.10:g.40730536_40730539dup
GRCh38.p14 chr 15	NC_000015.10:g.40730535_40730539dup
GRCh38.p14 chr 15	NC_000015.10:g.40730534_40730539dup
GRCh38.p14 chr 15	NC_000015.10:g.40730533_40730539dup
GRCh38.p14 chr 15	NC_000015.10:g.40730532_40730539dup
GRCh38.p14 chr 15	NC_000015.10:g.40730522_40730539dup
GRCh38.p14 chr 15	NC_000015.10:g.40730521_40730539dup
GRCh38.p14 chr 15	NC_000015.10:g.40730539_40730540insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 15	NC_000015.10:g.40730539_40730540insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 15	NC_000015.10:g.40730539_40730540insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.41022725_41022737del
GRCh37.p13 chr 15	NC_000015.9:g.41022726_41022737del
GRCh37.p13 chr 15	NC_000015.9:g.41022728_41022737del
GRCh37.p13 chr 15	NC_000015.9:g.41022729_41022737del
GRCh37.p13 chr 15	NC_000015.9:g.41022732_41022737del
GRCh37.p13 chr 15	NC_000015.9:g.41022733_41022737del
GRCh37.p13 chr 15	NC_000015.9:g.41022734_41022737del
GRCh37.p13 chr 15	NC_000015.9:g.41022735_41022737del
GRCh37.p13 chr 15	NC_000015.9:g.41022736_41022737del
GRCh37.p13 chr 15	NC_000015.9:g.41022737del
GRCh37.p13 chr 15	NC_000015.9:g.41022719_41022737T[19]CTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 15	NC_000015.9:g.41022719_41022737T[19]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 15	NC_000015.9:g.41022737dup
GRCh37.p13 chr 15	NC_000015.9:g.41022736_41022737dup
GRCh37.p13 chr 15	NC_000015.9:g.41022735_41022737dup
GRCh37.p13 chr 15	NC_000015.9:g.41022734_41022737dup
GRCh37.p13 chr 15	NC_000015.9:g.41022733_41022737dup
GRCh37.p13 chr 15	NC_000015.9:g.41022732_41022737dup
GRCh37.p13 chr 15	NC_000015.9:g.41022731_41022737dup
GRCh37.p13 chr 15	NC_000015.9:g.41022730_41022737dup
GRCh37.p13 chr 15	NC_000015.9:g.41022720_41022737dup
GRCh37.p13 chr 15	NC_000015.9:g.41022719_41022737dup
GRCh37.p13 chr 15	NC_000015.9:g.41022737_41022738insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.41022737_41022738insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.41022737_41022738insTTTTTTTTTTTTTTTTTTTTTT
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40367_40379del
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40368_40379del
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40370_40379del
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40371_40379del
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40374_40379del
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40375_40379del
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40376_40379del
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40377_40379del
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40378_40379del
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40379del
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40361_40379T[19]CTTTTTTTTTTTTTTTTTTTTTTTT[1]
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40361_40379T[19]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40379dup
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40378_40379dup
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40377_40379dup
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40376_40379dup
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40375_40379dup
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40374_40379dup
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40373_40379dup
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40372_40379dup
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40362_40379dup
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40361_40379dup
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40379_40380insTTTTTTTTTTTTTTTTTTTT
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40379_40380insTTTTTTTTTTTTTTTTTTTTT
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40379_40380insTTTTTTTTTTTTTTTTTTTTTT

Gene: RAD51, RAD51 recombinase (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RAD51 transcript variant 4	NM_001164269.2:c.900-528_… NM_001164269.2:c.900-528_900-516del	N/A	Intron Variant
RAD51 transcript variant 3	NM_001164270.2:c.775-528_… NM_001164270.2:c.775-528_775-516del	N/A	Intron Variant
RAD51 transcript variant 1	NM_002875.5:c.897-528_897… NM_002875.5:c.897-528_897-516del	N/A	Intron Variant
RAD51 transcript variant 2	NM_133487.4:c.900-528_900… NM_133487.4:c.900-528_900-516del	N/A	Intron Variant
RAD51 transcript variant X1	XM_011521857.3:c.987-528_… XM_011521857.3:c.987-528_987-516del	N/A	Intron Variant
RAD51 transcript variant X4	XM_011521858.3:c.897-528_… XM_011521858.3:c.897-528_897-516del	N/A	Intron Variant
RAD51 transcript variant X3	XM_011521859.3:c.897-528_… XM_011521859.3:c.897-528_897-516del	N/A	Intron Variant
RAD51 transcript variant X2	XM_011521860.3:c.897-528_… XM_011521860.3:c.897-528_897-516del	N/A	Intron Variant
RAD51 transcript variant X5	XM_011521861.3:c.865-528_… XM_011521861.3:c.865-528_865-516del	N/A	Intron Variant
RAD51 transcript variant X6	XM_047432925.1:c.525-528_… XM_047432925.1:c.525-528_525-516del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₁₉=	del(T)₁₃	del(T)₁₂	del(T)₁₀	del(T)₉	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	insC(T)₂₄	insC(T)₃₉	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₁₈	dup(T)₁₉	ins(T)₂₀	ins(T)₂₁	ins(T)₂₂
GRCh38.p14 chr 15	NC_000015.10:g.40730521_40730539=	NC_000015.10:g.40730527_40730539del	NC_000015.10:g.40730528_40730539del	NC_000015.10:g.40730530_40730539del	NC_000015.10:g.40730531_40730539del	NC_000015.10:g.40730534_40730539del	NC_000015.10:g.40730535_40730539del	NC_000015.10:g.40730536_40730539del	NC_000015.10:g.40730537_40730539del	NC_000015.10:g.40730538_40730539del	NC_000015.10:g.40730539del	NC_000015.10:g.40730521_40730539T[19]CTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000015.10:g.40730521_40730539T[19]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000015.10:g.40730539dup	NC_000015.10:g.40730538_40730539dup	NC_000015.10:g.40730537_40730539dup	NC_000015.10:g.40730536_40730539dup	NC_000015.10:g.40730535_40730539dup	NC_000015.10:g.40730534_40730539dup	NC_000015.10:g.40730533_40730539dup	NC_000015.10:g.40730532_40730539dup	NC_000015.10:g.40730522_40730539dup	NC_000015.10:g.40730521_40730539dup	NC_000015.10:g.40730539_40730540insTTTTTTTTTTTTTTTTTTTT	NC_000015.10:g.40730539_40730540insTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:g.40730539_40730540insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.41022719_41022737=	NC_000015.9:g.41022725_41022737del	NC_000015.9:g.41022726_41022737del	NC_000015.9:g.41022728_41022737del	NC_000015.9:g.41022729_41022737del	NC_000015.9:g.41022732_41022737del	NC_000015.9:g.41022733_41022737del	NC_000015.9:g.41022734_41022737del	NC_000015.9:g.41022735_41022737del	NC_000015.9:g.41022736_41022737del	NC_000015.9:g.41022737del	NC_000015.9:g.41022719_41022737T[19]CTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000015.9:g.41022719_41022737T[19]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000015.9:g.41022737dup	NC_000015.9:g.41022736_41022737dup	NC_000015.9:g.41022735_41022737dup	NC_000015.9:g.41022734_41022737dup	NC_000015.9:g.41022733_41022737dup	NC_000015.9:g.41022732_41022737dup	NC_000015.9:g.41022731_41022737dup	NC_000015.9:g.41022730_41022737dup	NC_000015.9:g.41022720_41022737dup	NC_000015.9:g.41022719_41022737dup	NC_000015.9:g.41022737_41022738insTTTTTTTTTTTTTTTTTTTT	NC_000015.9:g.41022737_41022738insTTTTTTTTTTTTTTTTTTTTT	NC_000015.9:g.41022737_41022738insTTTTTTTTTTTTTTTTTTTTTT
RAD51 RefSeqGene (LRG_313)	NG_012120.1:g.40361_40379=	NG_012120.1:g.40367_40379del	NG_012120.1:g.40368_40379del	NG_012120.1:g.40370_40379del	NG_012120.1:g.40371_40379del	NG_012120.1:g.40374_40379del	NG_012120.1:g.40375_40379del	NG_012120.1:g.40376_40379del	NG_012120.1:g.40377_40379del	NG_012120.1:g.40378_40379del	NG_012120.1:g.40379del	NG_012120.1:g.40361_40379T[19]CTTTTTTTTTTTTTTTTTTTTTTTT[1]	NG_012120.1:g.40361_40379T[19]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NG_012120.1:g.40379dup	NG_012120.1:g.40378_40379dup	NG_012120.1:g.40377_40379dup	NG_012120.1:g.40376_40379dup	NG_012120.1:g.40375_40379dup	NG_012120.1:g.40374_40379dup	NG_012120.1:g.40373_40379dup	NG_012120.1:g.40372_40379dup	NG_012120.1:g.40362_40379dup	NG_012120.1:g.40361_40379dup	NG_012120.1:g.40379_40380insTTTTTTTTTTTTTTTTTTTT	NG_012120.1:g.40379_40380insTTTTTTTTTTTTTTTTTTTTT	NG_012120.1:g.40379_40380insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant 4	NM_001164269.1:c.900-534=	NM_001164269.1:c.900-528_900-516del	NM_001164269.1:c.900-527_900-516del	NM_001164269.1:c.900-525_900-516del	NM_001164269.1:c.900-524_900-516del	NM_001164269.1:c.900-521_900-516del	NM_001164269.1:c.900-520_900-516del	NM_001164269.1:c.900-519_900-516del	NM_001164269.1:c.900-518_900-516del	NM_001164269.1:c.900-517_900-516del	NM_001164269.1:c.900-516del	NM_001164269.1:c.900-516_900-515insCTTTTTTTTTTTTTTTTTTTTTTTT	NM_001164269.1:c.900-516_900-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001164269.1:c.900-516dup	NM_001164269.1:c.900-517_900-516dup	NM_001164269.1:c.900-518_900-516dup	NM_001164269.1:c.900-519_900-516dup	NM_001164269.1:c.900-520_900-516dup	NM_001164269.1:c.900-521_900-516dup	NM_001164269.1:c.900-522_900-516dup	NM_001164269.1:c.900-523_900-516dup	NM_001164269.1:c.900-533_900-516dup	NM_001164269.1:c.900-534_900-516dup	NM_001164269.1:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTT	NM_001164269.1:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTTT	NM_001164269.1:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant 4	NM_001164269.2:c.900-534=	NM_001164269.2:c.900-528_900-516del	NM_001164269.2:c.900-527_900-516del	NM_001164269.2:c.900-525_900-516del	NM_001164269.2:c.900-524_900-516del	NM_001164269.2:c.900-521_900-516del	NM_001164269.2:c.900-520_900-516del	NM_001164269.2:c.900-519_900-516del	NM_001164269.2:c.900-518_900-516del	NM_001164269.2:c.900-517_900-516del	NM_001164269.2:c.900-516del	NM_001164269.2:c.900-516_900-515insCTTTTTTTTTTTTTTTTTTTTTTTT	NM_001164269.2:c.900-516_900-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001164269.2:c.900-516dup	NM_001164269.2:c.900-517_900-516dup	NM_001164269.2:c.900-518_900-516dup	NM_001164269.2:c.900-519_900-516dup	NM_001164269.2:c.900-520_900-516dup	NM_001164269.2:c.900-521_900-516dup	NM_001164269.2:c.900-522_900-516dup	NM_001164269.2:c.900-523_900-516dup	NM_001164269.2:c.900-533_900-516dup	NM_001164269.2:c.900-534_900-516dup	NM_001164269.2:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTT	NM_001164269.2:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTTT	NM_001164269.2:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant 3	NM_001164270.1:c.775-534=	NM_001164270.1:c.775-528_775-516del	NM_001164270.1:c.775-527_775-516del	NM_001164270.1:c.775-525_775-516del	NM_001164270.1:c.775-524_775-516del	NM_001164270.1:c.775-521_775-516del	NM_001164270.1:c.775-520_775-516del	NM_001164270.1:c.775-519_775-516del	NM_001164270.1:c.775-518_775-516del	NM_001164270.1:c.775-517_775-516del	NM_001164270.1:c.775-516del	NM_001164270.1:c.775-516_775-515insCTTTTTTTTTTTTTTTTTTTTTTTT	NM_001164270.1:c.775-516_775-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001164270.1:c.775-516dup	NM_001164270.1:c.775-517_775-516dup	NM_001164270.1:c.775-518_775-516dup	NM_001164270.1:c.775-519_775-516dup	NM_001164270.1:c.775-520_775-516dup	NM_001164270.1:c.775-521_775-516dup	NM_001164270.1:c.775-522_775-516dup	NM_001164270.1:c.775-523_775-516dup	NM_001164270.1:c.775-533_775-516dup	NM_001164270.1:c.775-534_775-516dup	NM_001164270.1:c.775-516_775-515insTTTTTTTTTTTTTTTTTTTT	NM_001164270.1:c.775-516_775-515insTTTTTTTTTTTTTTTTTTTTT	NM_001164270.1:c.775-516_775-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant 3	NM_001164270.2:c.775-534=	NM_001164270.2:c.775-528_775-516del	NM_001164270.2:c.775-527_775-516del	NM_001164270.2:c.775-525_775-516del	NM_001164270.2:c.775-524_775-516del	NM_001164270.2:c.775-521_775-516del	NM_001164270.2:c.775-520_775-516del	NM_001164270.2:c.775-519_775-516del	NM_001164270.2:c.775-518_775-516del	NM_001164270.2:c.775-517_775-516del	NM_001164270.2:c.775-516del	NM_001164270.2:c.775-516_775-515insCTTTTTTTTTTTTTTTTTTTTTTTT	NM_001164270.2:c.775-516_775-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001164270.2:c.775-516dup	NM_001164270.2:c.775-517_775-516dup	NM_001164270.2:c.775-518_775-516dup	NM_001164270.2:c.775-519_775-516dup	NM_001164270.2:c.775-520_775-516dup	NM_001164270.2:c.775-521_775-516dup	NM_001164270.2:c.775-522_775-516dup	NM_001164270.2:c.775-523_775-516dup	NM_001164270.2:c.775-533_775-516dup	NM_001164270.2:c.775-534_775-516dup	NM_001164270.2:c.775-516_775-515insTTTTTTTTTTTTTTTTTTTT	NM_001164270.2:c.775-516_775-515insTTTTTTTTTTTTTTTTTTTTT	NM_001164270.2:c.775-516_775-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant 1	NM_002875.4:c.897-534=	NM_002875.4:c.897-528_897-516del	NM_002875.4:c.897-527_897-516del	NM_002875.4:c.897-525_897-516del	NM_002875.4:c.897-524_897-516del	NM_002875.4:c.897-521_897-516del	NM_002875.4:c.897-520_897-516del	NM_002875.4:c.897-519_897-516del	NM_002875.4:c.897-518_897-516del	NM_002875.4:c.897-517_897-516del	NM_002875.4:c.897-516del	NM_002875.4:c.897-516_897-515insCTTTTTTTTTTTTTTTTTTTTTTTT	NM_002875.4:c.897-516_897-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_002875.4:c.897-516dup	NM_002875.4:c.897-517_897-516dup	NM_002875.4:c.897-518_897-516dup	NM_002875.4:c.897-519_897-516dup	NM_002875.4:c.897-520_897-516dup	NM_002875.4:c.897-521_897-516dup	NM_002875.4:c.897-522_897-516dup	NM_002875.4:c.897-523_897-516dup	NM_002875.4:c.897-533_897-516dup	NM_002875.4:c.897-534_897-516dup	NM_002875.4:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTT	NM_002875.4:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTTT	NM_002875.4:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant 1	NM_002875.5:c.897-534=	NM_002875.5:c.897-528_897-516del	NM_002875.5:c.897-527_897-516del	NM_002875.5:c.897-525_897-516del	NM_002875.5:c.897-524_897-516del	NM_002875.5:c.897-521_897-516del	NM_002875.5:c.897-520_897-516del	NM_002875.5:c.897-519_897-516del	NM_002875.5:c.897-518_897-516del	NM_002875.5:c.897-517_897-516del	NM_002875.5:c.897-516del	NM_002875.5:c.897-516_897-515insCTTTTTTTTTTTTTTTTTTTTTTTT	NM_002875.5:c.897-516_897-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_002875.5:c.897-516dup	NM_002875.5:c.897-517_897-516dup	NM_002875.5:c.897-518_897-516dup	NM_002875.5:c.897-519_897-516dup	NM_002875.5:c.897-520_897-516dup	NM_002875.5:c.897-521_897-516dup	NM_002875.5:c.897-522_897-516dup	NM_002875.5:c.897-523_897-516dup	NM_002875.5:c.897-533_897-516dup	NM_002875.5:c.897-534_897-516dup	NM_002875.5:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTT	NM_002875.5:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTTT	NM_002875.5:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant 2	NM_133487.3:c.900-534=	NM_133487.3:c.900-528_900-516del	NM_133487.3:c.900-527_900-516del	NM_133487.3:c.900-525_900-516del	NM_133487.3:c.900-524_900-516del	NM_133487.3:c.900-521_900-516del	NM_133487.3:c.900-520_900-516del	NM_133487.3:c.900-519_900-516del	NM_133487.3:c.900-518_900-516del	NM_133487.3:c.900-517_900-516del	NM_133487.3:c.900-516del	NM_133487.3:c.900-516_900-515insCTTTTTTTTTTTTTTTTTTTTTTTT	NM_133487.3:c.900-516_900-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_133487.3:c.900-516dup	NM_133487.3:c.900-517_900-516dup	NM_133487.3:c.900-518_900-516dup	NM_133487.3:c.900-519_900-516dup	NM_133487.3:c.900-520_900-516dup	NM_133487.3:c.900-521_900-516dup	NM_133487.3:c.900-522_900-516dup	NM_133487.3:c.900-523_900-516dup	NM_133487.3:c.900-533_900-516dup	NM_133487.3:c.900-534_900-516dup	NM_133487.3:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTT	NM_133487.3:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTTT	NM_133487.3:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant 2	NM_133487.4:c.900-534=	NM_133487.4:c.900-528_900-516del	NM_133487.4:c.900-527_900-516del	NM_133487.4:c.900-525_900-516del	NM_133487.4:c.900-524_900-516del	NM_133487.4:c.900-521_900-516del	NM_133487.4:c.900-520_900-516del	NM_133487.4:c.900-519_900-516del	NM_133487.4:c.900-518_900-516del	NM_133487.4:c.900-517_900-516del	NM_133487.4:c.900-516del	NM_133487.4:c.900-516_900-515insCTTTTTTTTTTTTTTTTTTTTTTTT	NM_133487.4:c.900-516_900-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_133487.4:c.900-516dup	NM_133487.4:c.900-517_900-516dup	NM_133487.4:c.900-518_900-516dup	NM_133487.4:c.900-519_900-516dup	NM_133487.4:c.900-520_900-516dup	NM_133487.4:c.900-521_900-516dup	NM_133487.4:c.900-522_900-516dup	NM_133487.4:c.900-523_900-516dup	NM_133487.4:c.900-533_900-516dup	NM_133487.4:c.900-534_900-516dup	NM_133487.4:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTT	NM_133487.4:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTTT	NM_133487.4:c.900-516_900-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant X1	XM_011521857.3:c.987-534=	XM_011521857.3:c.987-528_987-516del	XM_011521857.3:c.987-527_987-516del	XM_011521857.3:c.987-525_987-516del	XM_011521857.3:c.987-524_987-516del	XM_011521857.3:c.987-521_987-516del	XM_011521857.3:c.987-520_987-516del	XM_011521857.3:c.987-519_987-516del	XM_011521857.3:c.987-518_987-516del	XM_011521857.3:c.987-517_987-516del	XM_011521857.3:c.987-516del	XM_011521857.3:c.987-516_987-515insCTTTTTTTTTTTTTTTTTTTTTTTT	XM_011521857.3:c.987-516_987-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011521857.3:c.987-516dup	XM_011521857.3:c.987-517_987-516dup	XM_011521857.3:c.987-518_987-516dup	XM_011521857.3:c.987-519_987-516dup	XM_011521857.3:c.987-520_987-516dup	XM_011521857.3:c.987-521_987-516dup	XM_011521857.3:c.987-522_987-516dup	XM_011521857.3:c.987-523_987-516dup	XM_011521857.3:c.987-533_987-516dup	XM_011521857.3:c.987-534_987-516dup	XM_011521857.3:c.987-516_987-515insTTTTTTTTTTTTTTTTTTTT	XM_011521857.3:c.987-516_987-515insTTTTTTTTTTTTTTTTTTTTT	XM_011521857.3:c.987-516_987-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant X4	XM_011521858.3:c.897-534=	XM_011521858.3:c.897-528_897-516del	XM_011521858.3:c.897-527_897-516del	XM_011521858.3:c.897-525_897-516del	XM_011521858.3:c.897-524_897-516del	XM_011521858.3:c.897-521_897-516del	XM_011521858.3:c.897-520_897-516del	XM_011521858.3:c.897-519_897-516del	XM_011521858.3:c.897-518_897-516del	XM_011521858.3:c.897-517_897-516del	XM_011521858.3:c.897-516del	XM_011521858.3:c.897-516_897-515insCTTTTTTTTTTTTTTTTTTTTTTTT	XM_011521858.3:c.897-516_897-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011521858.3:c.897-516dup	XM_011521858.3:c.897-517_897-516dup	XM_011521858.3:c.897-518_897-516dup	XM_011521858.3:c.897-519_897-516dup	XM_011521858.3:c.897-520_897-516dup	XM_011521858.3:c.897-521_897-516dup	XM_011521858.3:c.897-522_897-516dup	XM_011521858.3:c.897-523_897-516dup	XM_011521858.3:c.897-533_897-516dup	XM_011521858.3:c.897-534_897-516dup	XM_011521858.3:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTT	XM_011521858.3:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTTT	XM_011521858.3:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant X3	XM_011521859.3:c.897-534=	XM_011521859.3:c.897-528_897-516del	XM_011521859.3:c.897-527_897-516del	XM_011521859.3:c.897-525_897-516del	XM_011521859.3:c.897-524_897-516del	XM_011521859.3:c.897-521_897-516del	XM_011521859.3:c.897-520_897-516del	XM_011521859.3:c.897-519_897-516del	XM_011521859.3:c.897-518_897-516del	XM_011521859.3:c.897-517_897-516del	XM_011521859.3:c.897-516del	XM_011521859.3:c.897-516_897-515insCTTTTTTTTTTTTTTTTTTTTTTTT	XM_011521859.3:c.897-516_897-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011521859.3:c.897-516dup	XM_011521859.3:c.897-517_897-516dup	XM_011521859.3:c.897-518_897-516dup	XM_011521859.3:c.897-519_897-516dup	XM_011521859.3:c.897-520_897-516dup	XM_011521859.3:c.897-521_897-516dup	XM_011521859.3:c.897-522_897-516dup	XM_011521859.3:c.897-523_897-516dup	XM_011521859.3:c.897-533_897-516dup	XM_011521859.3:c.897-534_897-516dup	XM_011521859.3:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTT	XM_011521859.3:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTTT	XM_011521859.3:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant X2	XM_011521860.3:c.897-534=	XM_011521860.3:c.897-528_897-516del	XM_011521860.3:c.897-527_897-516del	XM_011521860.3:c.897-525_897-516del	XM_011521860.3:c.897-524_897-516del	XM_011521860.3:c.897-521_897-516del	XM_011521860.3:c.897-520_897-516del	XM_011521860.3:c.897-519_897-516del	XM_011521860.3:c.897-518_897-516del	XM_011521860.3:c.897-517_897-516del	XM_011521860.3:c.897-516del	XM_011521860.3:c.897-516_897-515insCTTTTTTTTTTTTTTTTTTTTTTTT	XM_011521860.3:c.897-516_897-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011521860.3:c.897-516dup	XM_011521860.3:c.897-517_897-516dup	XM_011521860.3:c.897-518_897-516dup	XM_011521860.3:c.897-519_897-516dup	XM_011521860.3:c.897-520_897-516dup	XM_011521860.3:c.897-521_897-516dup	XM_011521860.3:c.897-522_897-516dup	XM_011521860.3:c.897-523_897-516dup	XM_011521860.3:c.897-533_897-516dup	XM_011521860.3:c.897-534_897-516dup	XM_011521860.3:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTT	XM_011521860.3:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTTT	XM_011521860.3:c.897-516_897-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant X5	XM_011521861.3:c.865-534=	XM_011521861.3:c.865-528_865-516del	XM_011521861.3:c.865-527_865-516del	XM_011521861.3:c.865-525_865-516del	XM_011521861.3:c.865-524_865-516del	XM_011521861.3:c.865-521_865-516del	XM_011521861.3:c.865-520_865-516del	XM_011521861.3:c.865-519_865-516del	XM_011521861.3:c.865-518_865-516del	XM_011521861.3:c.865-517_865-516del	XM_011521861.3:c.865-516del	XM_011521861.3:c.865-516_865-515insCTTTTTTTTTTTTTTTTTTTTTTTT	XM_011521861.3:c.865-516_865-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_011521861.3:c.865-516dup	XM_011521861.3:c.865-517_865-516dup	XM_011521861.3:c.865-518_865-516dup	XM_011521861.3:c.865-519_865-516dup	XM_011521861.3:c.865-520_865-516dup	XM_011521861.3:c.865-521_865-516dup	XM_011521861.3:c.865-522_865-516dup	XM_011521861.3:c.865-523_865-516dup	XM_011521861.3:c.865-533_865-516dup	XM_011521861.3:c.865-534_865-516dup	XM_011521861.3:c.865-516_865-515insTTTTTTTTTTTTTTTTTTTT	XM_011521861.3:c.865-516_865-515insTTTTTTTTTTTTTTTTTTTTT	XM_011521861.3:c.865-516_865-515insTTTTTTTTTTTTTTTTTTTTTT
RAD51 transcript variant X6	XM_047432925.1:c.525-534=	XM_047432925.1:c.525-528_525-516del	XM_047432925.1:c.525-527_525-516del	XM_047432925.1:c.525-525_525-516del	XM_047432925.1:c.525-524_525-516del	XM_047432925.1:c.525-521_525-516del	XM_047432925.1:c.525-520_525-516del	XM_047432925.1:c.525-519_525-516del	XM_047432925.1:c.525-518_525-516del	XM_047432925.1:c.525-517_525-516del	XM_047432925.1:c.525-516del	XM_047432925.1:c.525-516_525-515insCTTTTTTTTTTTTTTTTTTTTTTTT	XM_047432925.1:c.525-516_525-515insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047432925.1:c.525-516dup	XM_047432925.1:c.525-517_525-516dup	XM_047432925.1:c.525-518_525-516dup	XM_047432925.1:c.525-519_525-516dup	XM_047432925.1:c.525-520_525-516dup	XM_047432925.1:c.525-521_525-516dup	XM_047432925.1:c.525-522_525-516dup	XM_047432925.1:c.525-523_525-516dup	XM_047432925.1:c.525-533_525-516dup	XM_047432925.1:c.525-534_525-516dup	XM_047432925.1:c.525-516_525-515insTTTTTTTTTTTTTTTTTTTT	XM_047432925.1:c.525-516_525-515insTTTTTTTTTTTTTTTTTTTTT	XM_047432925.1:c.525-516_525-515insTTTTTTTTTTTTTTTTTTTTTT

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#.

43 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_GENOME_DK	ss1576752405	Apr 01, 2015 (144)
2	SWEGEN	ss3013157819	Nov 08, 2017 (151)
3	EVA_DECODE	ss3697745805	Jul 13, 2019 (153)
4	EVA_DECODE	ss3697745806	Jul 13, 2019 (153)
5	EVA_DECODE	ss3697745807	Jul 13, 2019 (153)
6	EVA_DECODE	ss3697745808	Jul 13, 2019 (153)
7	KOGIC	ss3975984808	Apr 27, 2020 (154)
8	KOGIC	ss3975984810	Apr 27, 2020 (154)
9	KOGIC	ss3975984812	Apr 27, 2020 (154)
10	GNOMAD	ss4287403330	Apr 26, 2021 (155)
11	GNOMAD	ss4287403331	Apr 26, 2021 (155)
12	GNOMAD	ss4287403332	Apr 26, 2021 (155)
13	GNOMAD	ss4287403333	Apr 26, 2021 (155)
14	GNOMAD	ss4287403334	Apr 26, 2021 (155)
15	GNOMAD	ss4287403335	Apr 26, 2021 (155)
16	GNOMAD	ss4287403336	Apr 26, 2021 (155)
17	GNOMAD	ss4287403337	Apr 26, 2021 (155)
18	GNOMAD	ss4287403363	Apr 26, 2021 (155)
19	GNOMAD	ss4287403366	Apr 26, 2021 (155)
20	GNOMAD	ss4287403367	Apr 26, 2021 (155)
21	GNOMAD	ss4287403368	Apr 26, 2021 (155)
22	GNOMAD	ss4287403369	Apr 26, 2021 (155)
23	GNOMAD	ss4287403370	Apr 26, 2021 (155)
24	GNOMAD	ss4287403371	Apr 26, 2021 (155)
25	GNOMAD	ss4287403372	Apr 26, 2021 (155)
26	GNOMAD	ss4287403373	Apr 26, 2021 (155)
27	GNOMAD	ss4287403374	Apr 26, 2021 (155)
28	GNOMAD	ss4287403375	Apr 26, 2021 (155)
29	GNOMAD	ss4287403376	Apr 26, 2021 (155)
30	GNOMAD	ss4287403377	Apr 26, 2021 (155)
31	GNOMAD	ss4287403378	Apr 26, 2021 (155)
32	GNOMAD	ss4287403379	Apr 26, 2021 (155)
33	GNOMAD	ss4287403380	Apr 26, 2021 (155)
34	GNOMAD	ss4287403381	Apr 26, 2021 (155)
35	TOPMED	ss4988627974	Apr 26, 2021 (155)
36	TOPMED	ss4988627975	Apr 26, 2021 (155)
37	HUGCELL_USP	ss5491932402	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5491932403	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5491932405	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5491932406	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5769522789	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5769522790	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5769522791	Oct 16, 2022 (156)
44	The Danish reference pan genome	NC_000015.9 - 41022719	Apr 27, 2020 (154)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 466772905 (NC_000015.10:40730520::T 891/103886) Row 466772906 (NC_000015.10:40730520::TT 18/103864) Row 466772907 (NC_000015.10:40730520::TTT 7/103876)...	-	Apr 26, 2021 (155)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 32362809 (NC_000015.10:40730522:T: 187/1828) Row 32362811 (NC_000015.10:40730521:TT: 51/1828) Row 32362813 (NC_000015.10:40730520:TTT: 4/1828)	-	Apr 27, 2020 (154)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 32362809 (NC_000015.10:40730522:T: 187/1828) Row 32362811 (NC_000015.10:40730521:TT: 51/1828) Row 32362813 (NC_000015.10:40730520:TTT: 4/1828)	-	Apr 27, 2020 (154)
72	Korean Genome Project Submission ignored due to conflicting rows: Row 32362809 (NC_000015.10:40730522:T: 187/1828) Row 32362811 (NC_000015.10:40730521:TT: 51/1828) Row 32362813 (NC_000015.10:40730520:TTT: 4/1828)	-	Apr 27, 2020 (154)
73	14KJPN Submission ignored due to conflicting rows: Row 103359893 (NC_000015.10:40730520:TT: 829/27132) Row 103359894 (NC_000015.10:40730520:T: 2891/27132) Row 103359895 (NC_000015.10:40730520::TTTTTTTTTTTTTTTTTTT 6/27132)	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 103359893 (NC_000015.10:40730520:TT: 829/27132) Row 103359894 (NC_000015.10:40730520:T: 2891/27132) Row 103359895 (NC_000015.10:40730520::TTTTTTTTTTTTTTTTTTT 6/27132)	-	Oct 16, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 103359893 (NC_000015.10:40730520:TT: 829/27132) Row 103359894 (NC_000015.10:40730520:T: 2891/27132) Row 103359895 (NC_000015.10:40730520::TTTTTTTTTTTTTTTTTTT 6/27132)	-	Oct 16, 2022 (156)
76	TopMed Submission ignored due to conflicting rows: Row 204173634 (NC_000015.10:40730520:TTTTTTTTTT: 1/264690) Row 204173635 (NC_000015.10:40730520:TTTTTTTTTTTT: 23/264690)	-	Apr 26, 2021 (155)
77	TopMed Submission ignored due to conflicting rows: Row 204173634 (NC_000015.10:40730520:TTTTTTTTTT: 1/264690) Row 204173635 (NC_000015.10:40730520:TTTTTTTTTTTT: 23/264690)	-	Apr 26, 2021 (155)
78	ALFA	NC_000015.10 - 40730521	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4287403381	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTT:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTT	(self)
7967982523	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTT	(self)
ss4287403380, ss4988627975	NC_000015.10:40730520:TTTTTTTTTTTT:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTT	(self)
7967982523	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTT	(self)
ss4287403379, ss4988627974	NC_000015.10:40730520:TTTTTTTTTT:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
7967982523	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4287403378	NC_000015.10:40730520:TTTTTTTTT:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4287403377	NC_000015.10:40730520:TTTTTT:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4287403376, ss5491932406	NC_000015.10:40730520:TTTTT:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
7967982523	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4287403375	NC_000015.10:40730520:TTTT:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7967982523	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3975984812, ss4287403374	NC_000015.10:40730520:TTT:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
7967982523	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3697745805, ss4287403373, ss5491932405, ss5769522789	NC_000015.10:40730520:TT:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
7967982523	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3975984810	NC_000015.10:40730521:TT:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3013157819	NC_000015.9:41022718:T:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4287403372, ss5491932402, ss5769522790	NC_000015.10:40730520:T:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
7967982523	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3697745806	NC_000015.10:40730521:T:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3975984808	NC_000015.10:40730522:T:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4287403367	NC_000015.10:40730520::TTTTTTTTTTT… NC_000015.10:40730520::TTTTTTTTTTTTTTTTTTTCTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403368	NC_000015.10:40730520::TTTTTTTTTTT… NC_000015.10:40730520::TTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403330, ss5491932403	NC_000015.10:40730520::T	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
7967982523	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3697745807	NC_000015.10:40730522::T	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4287403331	NC_000015.10:40730520::TT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
7967982523	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3697745808	NC_000015.10:40730522::TT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403332	NC_000015.10:40730520::TTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403333	NC_000015.10:40730520::TTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403334	NC_000015.10:40730520::TTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403335	NC_000015.10:40730520::TTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403336	NC_000015.10:40730520::TTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403337	NC_000015.10:40730520::TTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403363	NC_000015.10:40730520::TTTTTTTTTTT… NC_000015.10:40730520::TTTTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
35277, ss1576752405	NC_000015.9:41022718::TTTTTTTTTTTT… NC_000015.9:41022718::TTTTTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403366, ss5769522791	NC_000015.10:40730520::TTTTTTTTTTT… NC_000015.10:40730520::TTTTTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403369	NC_000015.10:40730520::TTTTTTTTTTT… NC_000015.10:40730520::TTTTTTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403370	NC_000015.10:40730520::TTTTTTTTTTT… NC_000015.10:40730520::TTTTTTTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4287403371	NC_000015.10:40730520::TTTTTTTTTTT… NC_000015.10:40730520::TTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2370788600	NC_000015.9:41022718:TTTTT:	NC_000015.10:40730520:TTTTTTTTTTTT… NC_000015.10:40730520:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

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

No publications for rs778467789

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

rs778467789