Name: rs778728861
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.

rs778728861

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:76603828-76603844 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₅ / delTTT / delTT / delT / …
del(T)₅ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂
Variation Type: Indel Insertion and Deletion
Frequency: dup(T)₅=0.0936 (729/7788, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC03009 : 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	7788	TTTTTTTTTTTTTTTTT=0.8218	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0021, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0014, TTTTTTTTTTTTTTTTTTTTTT=0.0936, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0794, TTTTTTTTTTTTTTTTTTTTTTT=0.0008, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0010, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.862757	0.039595	0.097648	32
European	Sub	6784	TTTTTTTTTTTTTTTTT=0.7963	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0024, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0016, TTTTTTTTTTTTTTTTTTTTTT=0.1070, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0907, TTTTTTTTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.839105	0.04617	0.114725	32
African	Sub	610	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	20	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	590	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	36	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	28	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	38	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	180	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	16	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	124	TTTTTTTTTTTTTTTTT=0.952	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.024, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.024, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.983333	0.016667	0.0	32

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	7788	(T)₁₇=0.8218	del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0021, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0014, dup(T)₅=0.0936, dup(T)₆=0.0008, dup(T)₇=0.0000, dup(T)₈=0.0010, dup(T)₉=0.0794, dup(T)₁₀=0.0000
Allele Frequency Aggregator	European	Sub	6784	(T)₁₇=0.7963	del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0024, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0016, dup(T)₅=0.1070, dup(T)₆=0.0009, dup(T)₇=0.0000, dup(T)₈=0.0012, dup(T)₉=0.0907, dup(T)₁₀=0.0000
Allele Frequency Aggregator	African	Sub	610	(T)₁₇=1.000	del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000
Allele Frequency Aggregator	Latin American 2	Sub	180	(T)₁₇=1.000	del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000
Allele Frequency Aggregator	Other	Sub	124	(T)₁₇=0.952	del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.024, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.024, dup(T)₁₀=0.000
Allele Frequency Aggregator	Latin American 1	Sub	38	(T)₁₇=1.00	del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00
Allele Frequency Aggregator	Asian	Sub	36	(T)₁₇=1.00	del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00
Allele Frequency Aggregator	South Asian	Sub	16	(T)₁₇=1.00	del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)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 7	NC_000007.14:g.76603840_76603844del
GRCh38.p14 chr 7	NC_000007.14:g.76603842_76603844del
GRCh38.p14 chr 7	NC_000007.14:g.76603843_76603844del
GRCh38.p14 chr 7	NC_000007.14:g.76603844del
GRCh38.p14 chr 7	NC_000007.14:g.76603844dup
GRCh38.p14 chr 7	NC_000007.14:g.76603843_76603844dup
GRCh38.p14 chr 7	NC_000007.14:g.76603842_76603844dup
GRCh38.p14 chr 7	NC_000007.14:g.76603841_76603844dup
GRCh38.p14 chr 7	NC_000007.14:g.76603840_76603844dup
GRCh38.p14 chr 7	NC_000007.14:g.76603839_76603844dup
GRCh38.p14 chr 7	NC_000007.14:g.76603838_76603844dup
GRCh38.p14 chr 7	NC_000007.14:g.76603837_76603844dup
GRCh38.p14 chr 7	NC_000007.14:g.76603836_76603844dup
GRCh38.p14 chr 7	NC_000007.14:g.76603835_76603844dup
GRCh38.p14 chr 7	NC_000007.14:g.76603834_76603844dup
GRCh38.p14 chr 7	NC_000007.14:g.76603833_76603844dup
GRCh37.p13 chr 7	NC_000007.13:g.76233157_76233161del
GRCh37.p13 chr 7	NC_000007.13:g.76233159_76233161del
GRCh37.p13 chr 7	NC_000007.13:g.76233160_76233161del
GRCh37.p13 chr 7	NC_000007.13:g.76233161del
GRCh37.p13 chr 7	NC_000007.13:g.76233161dup
GRCh37.p13 chr 7	NC_000007.13:g.76233160_76233161dup
GRCh37.p13 chr 7	NC_000007.13:g.76233159_76233161dup
GRCh37.p13 chr 7	NC_000007.13:g.76233158_76233161dup
GRCh37.p13 chr 7	NC_000007.13:g.76233157_76233161dup
GRCh37.p13 chr 7	NC_000007.13:g.76233156_76233161dup
GRCh37.p13 chr 7	NC_000007.13:g.76233155_76233161dup
GRCh37.p13 chr 7	NC_000007.13:g.76233154_76233161dup
GRCh37.p13 chr 7	NC_000007.13:g.76233153_76233161dup
GRCh37.p13 chr 7	NC_000007.13:g.76233152_76233161dup
GRCh37.p13 chr 7	NC_000007.13:g.76233151_76233161dup
GRCh37.p13 chr 7	NC_000007.13:g.76233150_76233161dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90675_90679del
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90677_90679del
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90678_90679del
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90679del
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90679dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90678_90679dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90677_90679dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90676_90679dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90675_90679dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90674_90679dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90673_90679dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90672_90679dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90671_90679dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90670_90679dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90669_90679dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90668_90679dup

Gene: LINC03009, long intergenic non-protein coding RNA 3009 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC03009 transcript	NR_029411.1:n.	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)₁₇=	del(T)₅	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂
GRCh38.p14 chr 7	NC_000007.14:g.76603828_76603844=	NC_000007.14:g.76603840_76603844del	NC_000007.14:g.76603842_76603844del	NC_000007.14:g.76603843_76603844del	NC_000007.14:g.76603844del	NC_000007.14:g.76603844dup	NC_000007.14:g.76603843_76603844dup	NC_000007.14:g.76603842_76603844dup	NC_000007.14:g.76603841_76603844dup	NC_000007.14:g.76603840_76603844dup	NC_000007.14:g.76603839_76603844dup	NC_000007.14:g.76603838_76603844dup	NC_000007.14:g.76603837_76603844dup	NC_000007.14:g.76603836_76603844dup	NC_000007.14:g.76603835_76603844dup	NC_000007.14:g.76603834_76603844dup	NC_000007.14:g.76603833_76603844dup
GRCh37.p13 chr 7	NC_000007.13:g.76233145_76233161=	NC_000007.13:g.76233157_76233161del	NC_000007.13:g.76233159_76233161del	NC_000007.13:g.76233160_76233161del	NC_000007.13:g.76233161del	NC_000007.13:g.76233161dup	NC_000007.13:g.76233160_76233161dup	NC_000007.13:g.76233159_76233161dup	NC_000007.13:g.76233158_76233161dup	NC_000007.13:g.76233157_76233161dup	NC_000007.13:g.76233156_76233161dup	NC_000007.13:g.76233155_76233161dup	NC_000007.13:g.76233154_76233161dup	NC_000007.13:g.76233153_76233161dup	NC_000007.13:g.76233152_76233161dup	NC_000007.13:g.76233151_76233161dup	NC_000007.13:g.76233150_76233161dup
GRCh38.p14 chr 7 alt locus HSCHR7_2_CTG4_4	NT_187561.1:g.90663_90679=	NT_187561.1:g.90675_90679del	NT_187561.1:g.90677_90679del	NT_187561.1:g.90678_90679del	NT_187561.1:g.90679del	NT_187561.1:g.90679dup	NT_187561.1:g.90678_90679dup	NT_187561.1:g.90677_90679dup	NT_187561.1:g.90676_90679dup	NT_187561.1:g.90675_90679dup	NT_187561.1:g.90674_90679dup	NT_187561.1:g.90673_90679dup	NT_187561.1:g.90672_90679dup	NT_187561.1:g.90671_90679dup	NT_187561.1:g.90670_90679dup	NT_187561.1:g.90669_90679dup	NT_187561.1:g.90668_90679dup
LOC100505767 transcript variant X2	XM_005250741.1:c.830-63482=	XM_005250741.1:c.830-63486_830-63482del	XM_005250741.1:c.830-63484_830-63482del	XM_005250741.1:c.830-63483_830-63482del	XM_005250741.1:c.830-63482del	XM_005250741.1:c.830-63482dup	XM_005250741.1:c.830-63483_830-63482dup	XM_005250741.1:c.830-63484_830-63482dup	XM_005250741.1:c.830-63485_830-63482dup	XM_005250741.1:c.830-63486_830-63482dup	XM_005250741.1:c.830-63487_830-63482dup	XM_005250741.1:c.830-63488_830-63482dup	XM_005250741.1:c.830-63489_830-63482dup	XM_005250741.1:c.830-63490_830-63482dup	XM_005250741.1:c.830-63491_830-63482dup	XM_005250741.1:c.830-63492_830-63482dup	XM_005250741.1:c.830-63493_830-63482dup

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#.

50 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSMP	ss663799122	Apr 01, 2015 (144)
2	SWEGEN	ss3001451949	Nov 08, 2017 (151)
3	SWEGEN	ss3001451950	Nov 08, 2017 (151)
4	SWEGEN	ss3001451951	Nov 08, 2017 (151)
5	SWEGEN	ss3001451952	Nov 08, 2017 (151)
6	SWEGEN	ss3001451953	Nov 08, 2017 (151)
7	EVA_DECODE	ss3719999680	Jul 13, 2019 (153)
8	EVA_DECODE	ss3719999681	Jul 13, 2019 (153)
9	EVA_DECODE	ss3719999682	Jul 13, 2019 (153)
10	EVA_DECODE	ss3719999683	Jul 13, 2019 (153)
11	EVA_DECODE	ss3719999684	Jul 13, 2019 (153)
12	EVA_DECODE	ss3719999685	Jul 13, 2019 (153)
13	PACBIO	ss3785863030	Jul 13, 2019 (153)
14	PACBIO	ss3796038122	Jul 13, 2019 (153)
15	GNOMAD	ss4166553975	Apr 26, 2021 (155)
16	GNOMAD	ss4166553976	Apr 26, 2021 (155)
17	GNOMAD	ss4166553977	Apr 26, 2021 (155)
18	GNOMAD	ss4166553979	Apr 26, 2021 (155)
19	GNOMAD	ss4166553980	Apr 26, 2021 (155)
20	GNOMAD	ss4166553981	Apr 26, 2021 (155)
21	GNOMAD	ss4166553982	Apr 26, 2021 (155)
22	GNOMAD	ss4166553983	Apr 26, 2021 (155)
23	GNOMAD	ss4166553984	Apr 26, 2021 (155)
24	GNOMAD	ss4166553985	Apr 26, 2021 (155)
25	GNOMAD	ss4166553986	Apr 26, 2021 (155)
26	GNOMAD	ss4166553987	Apr 26, 2021 (155)
27	GNOMAD	ss4166553989	Apr 26, 2021 (155)
28	GNOMAD	ss4166553990	Apr 26, 2021 (155)
29	GNOMAD	ss4166553991	Apr 26, 2021 (155)
30	GNOMAD	ss4166553992	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5183938174	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5183938175	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5183938176	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5183938177	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5183938178	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5183938179	Apr 26, 2021 (155)
37	1000G_HIGH_COVERAGE	ss5273478643	Oct 13, 2022 (156)
38	HUGCELL_USP	ss5470509124	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5470509125	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5470509126	Oct 13, 2022 (156)
41	HUGCELL_USP	ss5470509127	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5470509128	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5470509129	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5724436067	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5724436068	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5724436069	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5724436070	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5724436071	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5724436072	Oct 13, 2022 (156)
50	EVA	ss5855957446	Oct 13, 2022 (156)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265957261 (NC_000007.14:76603827::T 825/106886) Row 265957262 (NC_000007.14:76603827::TT 54/106924) Row 265957263 (NC_000007.14:76603827::TTT 12/106918)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 41907481 (NC_000007.13:76233144::TTTTT 4647/16556) Row 41907482 (NC_000007.13:76233144::TTTTTTTTT 172/16556) Row 41907483 (NC_000007.13:76233144::TTTTTT 48/16556)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 41907481 (NC_000007.13:76233144::TTTTT 4647/16556) Row 41907482 (NC_000007.13:76233144::TTTTTTTTT 172/16556) Row 41907483 (NC_000007.13:76233144::TTTTTT 48/16556)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 41907481 (NC_000007.13:76233144::TTTTT 4647/16556) Row 41907482 (NC_000007.13:76233144::TTTTTTTTT 172/16556) Row 41907483 (NC_000007.13:76233144::TTTTTT 48/16556)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 41907481 (NC_000007.13:76233144::TTTTT 4647/16556) Row 41907482 (NC_000007.13:76233144::TTTTTTTTT 172/16556) Row 41907483 (NC_000007.13:76233144::TTTTTT 48/16556)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 41907481 (NC_000007.13:76233144::TTTTT 4647/16556) Row 41907482 (NC_000007.13:76233144::TTTTTTTTT 172/16556) Row 41907483 (NC_000007.13:76233144::TTTTTT 48/16556)...	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 41907481 (NC_000007.13:76233144::TTTTT 4647/16556) Row 41907482 (NC_000007.13:76233144::TTTTTTTTT 172/16556) Row 41907483 (NC_000007.13:76233144::TTTTTT 48/16556)...	-	Apr 26, 2021 (155)
73	14KJPN Submission ignored due to conflicting rows: Row 58273171 (NC_000007.14:76603827::TTTTT 7190/27742) Row 58273172 (NC_000007.14:76603827:T: 57/27742) Row 58273173 (NC_000007.14:76603827:TT: 36/27742)...	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 58273171 (NC_000007.14:76603827::TTTTT 7190/27742) Row 58273172 (NC_000007.14:76603827:T: 57/27742) Row 58273173 (NC_000007.14:76603827:TT: 36/27742)...	-	Oct 13, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 58273171 (NC_000007.14:76603827::TTTTT 7190/27742) Row 58273172 (NC_000007.14:76603827:T: 57/27742) Row 58273173 (NC_000007.14:76603827:TT: 36/27742)...	-	Oct 13, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 58273171 (NC_000007.14:76603827::TTTTT 7190/27742) Row 58273172 (NC_000007.14:76603827:T: 57/27742) Row 58273173 (NC_000007.14:76603827:TT: 36/27742)...	-	Oct 13, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 58273171 (NC_000007.14:76603827::TTTTT 7190/27742) Row 58273172 (NC_000007.14:76603827:T: 57/27742) Row 58273173 (NC_000007.14:76603827:TT: 36/27742)...	-	Oct 13, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 58273171 (NC_000007.14:76603827::TTTTT 7190/27742) Row 58273172 (NC_000007.14:76603827:T: 57/27742) Row 58273173 (NC_000007.14:76603827:TT: 36/27742)...	-	Oct 13, 2022 (156)
79	ALFA	NC_000007.14 - 76603828	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
ss4166553992	NC_000007.14:76603827:TTTTT:	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4166553991	NC_000007.14:76603827:TTT:	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5183938178	NC_000007.13:76233144:TT:	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4166553990, ss5724436069	NC_000007.14:76603827:TT:	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5183938179	NC_000007.13:76233144:T:	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3719999680, ss4166553989, ss5470509125, ss5724436068	NC_000007.14:76603827:T:	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3001451951, ss5183938177	NC_000007.13:76233144::T	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4166553975, ss5724436071, ss5855957446	NC_000007.14:76603827::T	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4166553976	NC_000007.14:76603827::TT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4166553977	NC_000007.14:76603827::TTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3719999681	NC_000007.14:76603828::TTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss663799122, ss3001451953	NC_000007.13:76233144::TTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4166553979, ss5470509126	NC_000007.14:76603827::TTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3719999682	NC_000007.14:76603828::TTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3001451950, ss5183938174	NC_000007.13:76233144::TTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4166553980, ss5273478643, ss5470509124, ss5724436067	NC_000007.14:76603827::TTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3719999683	NC_000007.14:76603828::TTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5183938176	NC_000007.13:76233144::TTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4166553981, ss5470509127, ss5724436072	NC_000007.14:76603827::TTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4166553982	NC_000007.14:76603827::TTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3785863030, ss3796038122	NC_000007.13:76233144::TTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4166553983, ss5470509128	NC_000007.14:76603827::TTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3719999684	NC_000007.14:76603828::TTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3001451949, ss5183938175	NC_000007.13:76233144::TTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4166553984, ss5470509129, ss5724436070	NC_000007.14:76603827::TTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3719999685	NC_000007.14:76603828::TTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3001451952	NC_000007.13:76233144::TTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4166553985	NC_000007.14:76603827::TTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7100385070	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4166553986	NC_000007.14:76603827::TTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4166553987	NC_000007.14:76603827::TTTTTTTTTTTT	NC_000007.14:76603827:TTTTTTTTTTTT… NC_000007.14:76603827:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs778728861

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

rs778728861