Name: rs1181597035
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.

rs1181597035

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:135854530-135854551 (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(A)₁₃ / del(A)₁₂ / del(A)₁₁ / d…
del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.0000 (0/8970, ALFA)
del(A)₉=0.0000 (0/8970, ALFA)
del(A)₈=0.0000 (0/8970, ALFA) (+ 10 more)
del(A)₇=0.0000 (0/8970, ALFA)
del(A)₆=0.0000 (0/8970, ALFA)
del(A)₅=0.0000 (0/8970, ALFA)
delAAA=0.0000 (0/8970, ALFA)
delAA=0.0000 (0/8970, ALFA)
delA=0.0000 (0/8970, ALFA)
dupA=0.0000 (0/8970, ALFA)
dupAA=0.0000 (0/8970, ALFA)
dupAAA=0.0000 (0/8970, ALFA)
dup(A)₄=0.0000 (0/8970, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MCM6 : 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	HWEP
Total	Global	8970	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	5382	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	2360	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	94	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	2266	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	94	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	70	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	24	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	126	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	546	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	84	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	378	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	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	8970	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	5382	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	2360	(A)₂₂=1.0000	del(A)₁₃=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	546	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	378	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	126	(A)₂₂=1.000	del(A)₁₃=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Asian	Sub	94	(A)₂₂=1.00	del(A)₁₃=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	84	(A)₂₂=1.00	del(A)₁₃=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=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 2	NC_000002.12:g.135854539_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854540_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854541_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854542_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854543_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854544_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854545_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854546_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854547_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854548_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854549_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854550_135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854551del
GRCh38.p14 chr 2	NC_000002.12:g.135854551dup
GRCh38.p14 chr 2	NC_000002.12:g.135854550_135854551dup
GRCh38.p14 chr 2	NC_000002.12:g.135854549_135854551dup
GRCh38.p14 chr 2	NC_000002.12:g.135854548_135854551dup
GRCh38.p14 chr 2	NC_000002.12:g.135854547_135854551dup
GRCh37.p13 chr 2	NC_000002.11:g.136612109_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612110_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612111_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612112_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612113_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612114_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612115_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612116_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612117_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612118_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612119_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612120_136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612121del
GRCh37.p13 chr 2	NC_000002.11:g.136612121dup
GRCh37.p13 chr 2	NC_000002.11:g.136612120_136612121dup
GRCh37.p13 chr 2	NC_000002.11:g.136612119_136612121dup
GRCh37.p13 chr 2	NC_000002.11:g.136612118_136612121dup
GRCh37.p13 chr 2	NC_000002.11:g.136612117_136612121dup
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5628_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5629_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5630_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5631_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5632_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5633_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5634_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5635_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5636_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5637_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5638_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5639_5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5640del
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5640dup
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5639_5640dup
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5638_5640dup
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5637_5640dup
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5636_5640dup
MCM6 RefSeqGene	NG_008958.1:g.26900_26912del
MCM6 RefSeqGene	NG_008958.1:g.26901_26912del
MCM6 RefSeqGene	NG_008958.1:g.26902_26912del
MCM6 RefSeqGene	NG_008958.1:g.26903_26912del
MCM6 RefSeqGene	NG_008958.1:g.26904_26912del
MCM6 RefSeqGene	NG_008958.1:g.26905_26912del
MCM6 RefSeqGene	NG_008958.1:g.26906_26912del
MCM6 RefSeqGene	NG_008958.1:g.26907_26912del
MCM6 RefSeqGene	NG_008958.1:g.26908_26912del
MCM6 RefSeqGene	NG_008958.1:g.26909_26912del
MCM6 RefSeqGene	NG_008958.1:g.26910_26912del
MCM6 RefSeqGene	NG_008958.1:g.26911_26912del
MCM6 RefSeqGene	NG_008958.1:g.26912del
MCM6 RefSeqGene	NG_008958.1:g.26912dup
MCM6 RefSeqGene	NG_008958.1:g.26911_26912dup
MCM6 RefSeqGene	NG_008958.1:g.26910_26912dup
MCM6 RefSeqGene	NG_008958.1:g.26909_26912dup
MCM6 RefSeqGene	NG_008958.1:g.26908_26912dup

Gene: MCM6, minichromosome maintenance complex component 6 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MCM6 transcript	NM_005915.6:c.1627-1627_1… NM_005915.6:c.1627-1627_1627-1615del	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	(A)₂₂=	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅
GRCh38.p14 chr 2	NC_000002.12:g.135854530_135854551=	NC_000002.12:g.135854539_135854551del	NC_000002.12:g.135854540_135854551del	NC_000002.12:g.135854541_135854551del	NC_000002.12:g.135854542_135854551del	NC_000002.12:g.135854543_135854551del	NC_000002.12:g.135854544_135854551del	NC_000002.12:g.135854545_135854551del	NC_000002.12:g.135854546_135854551del	NC_000002.12:g.135854547_135854551del	NC_000002.12:g.135854548_135854551del	NC_000002.12:g.135854549_135854551del	NC_000002.12:g.135854550_135854551del	NC_000002.12:g.135854551del	NC_000002.12:g.135854551dup	NC_000002.12:g.135854550_135854551dup	NC_000002.12:g.135854549_135854551dup	NC_000002.12:g.135854548_135854551dup	NC_000002.12:g.135854547_135854551dup
GRCh37.p13 chr 2	NC_000002.11:g.136612100_136612121=	NC_000002.11:g.136612109_136612121del	NC_000002.11:g.136612110_136612121del	NC_000002.11:g.136612111_136612121del	NC_000002.11:g.136612112_136612121del	NC_000002.11:g.136612113_136612121del	NC_000002.11:g.136612114_136612121del	NC_000002.11:g.136612115_136612121del	NC_000002.11:g.136612116_136612121del	NC_000002.11:g.136612117_136612121del	NC_000002.11:g.136612118_136612121del	NC_000002.11:g.136612119_136612121del	NC_000002.11:g.136612120_136612121del	NC_000002.11:g.136612121del	NC_000002.11:g.136612121dup	NC_000002.11:g.136612120_136612121dup	NC_000002.11:g.136612119_136612121dup	NC_000002.11:g.136612118_136612121dup	NC_000002.11:g.136612117_136612121dup
LCT RefSeqGene (LRG_338)	NG_008104.2:g.5619_5640=	NG_008104.2:g.5628_5640del	NG_008104.2:g.5629_5640del	NG_008104.2:g.5630_5640del	NG_008104.2:g.5631_5640del	NG_008104.2:g.5632_5640del	NG_008104.2:g.5633_5640del	NG_008104.2:g.5634_5640del	NG_008104.2:g.5635_5640del	NG_008104.2:g.5636_5640del	NG_008104.2:g.5637_5640del	NG_008104.2:g.5638_5640del	NG_008104.2:g.5639_5640del	NG_008104.2:g.5640del	NG_008104.2:g.5640dup	NG_008104.2:g.5639_5640dup	NG_008104.2:g.5638_5640dup	NG_008104.2:g.5637_5640dup	NG_008104.2:g.5636_5640dup
MCM6 RefSeqGene	NG_008958.1:g.26891_26912=	NG_008958.1:g.26900_26912del	NG_008958.1:g.26901_26912del	NG_008958.1:g.26902_26912del	NG_008958.1:g.26903_26912del	NG_008958.1:g.26904_26912del	NG_008958.1:g.26905_26912del	NG_008958.1:g.26906_26912del	NG_008958.1:g.26907_26912del	NG_008958.1:g.26908_26912del	NG_008958.1:g.26909_26912del	NG_008958.1:g.26910_26912del	NG_008958.1:g.26911_26912del	NG_008958.1:g.26912del	NG_008958.1:g.26912dup	NG_008958.1:g.26911_26912dup	NG_008958.1:g.26910_26912dup	NG_008958.1:g.26909_26912dup	NG_008958.1:g.26908_26912dup
MCM6 transcript	NM_005915.5:c.1627-1615=	NM_005915.5:c.1627-1627_1627-1615del	NM_005915.5:c.1627-1626_1627-1615del	NM_005915.5:c.1627-1625_1627-1615del	NM_005915.5:c.1627-1624_1627-1615del	NM_005915.5:c.1627-1623_1627-1615del	NM_005915.5:c.1627-1622_1627-1615del	NM_005915.5:c.1627-1621_1627-1615del	NM_005915.5:c.1627-1620_1627-1615del	NM_005915.5:c.1627-1619_1627-1615del	NM_005915.5:c.1627-1618_1627-1615del	NM_005915.5:c.1627-1617_1627-1615del	NM_005915.5:c.1627-1616_1627-1615del	NM_005915.5:c.1627-1615del	NM_005915.5:c.1627-1615dup	NM_005915.5:c.1627-1616_1627-1615dup	NM_005915.5:c.1627-1617_1627-1615dup	NM_005915.5:c.1627-1618_1627-1615dup	NM_005915.5:c.1627-1619_1627-1615dup
MCM6 transcript	NM_005915.6:c.1627-1615=	NM_005915.6:c.1627-1627_1627-1615del	NM_005915.6:c.1627-1626_1627-1615del	NM_005915.6:c.1627-1625_1627-1615del	NM_005915.6:c.1627-1624_1627-1615del	NM_005915.6:c.1627-1623_1627-1615del	NM_005915.6:c.1627-1622_1627-1615del	NM_005915.6:c.1627-1621_1627-1615del	NM_005915.6:c.1627-1620_1627-1615del	NM_005915.6:c.1627-1619_1627-1615del	NM_005915.6:c.1627-1618_1627-1615del	NM_005915.6:c.1627-1617_1627-1615del	NM_005915.6:c.1627-1616_1627-1615del	NM_005915.6:c.1627-1615del	NM_005915.6:c.1627-1615dup	NM_005915.6:c.1627-1616_1627-1615dup	NM_005915.6:c.1627-1617_1627-1615dup	NM_005915.6:c.1627-1618_1627-1615dup	NM_005915.6:c.1627-1619_1627-1615dup

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#.

41 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3704955030	Jul 13, 2019 (153)
2	EVA_DECODE	ss3704955031	Jul 13, 2019 (153)
3	EVA_DECODE	ss3704955032	Jul 13, 2019 (153)
4	EVA_DECODE	ss3704955033	Jul 13, 2019 (153)
5	EVA_DECODE	ss3704955034	Jul 13, 2019 (153)
6	EVA_DECODE	ss3704955035	Jul 13, 2019 (153)
7	KOGIC	ss3949036386	Apr 25, 2020 (154)
8	KOGIC	ss3949036387	Apr 25, 2020 (154)
9	KOGIC	ss3949036388	Apr 25, 2020 (154)
10	GNOMAD	ss4051322848	Apr 26, 2021 (155)
11	GNOMAD	ss4051322849	Apr 26, 2021 (155)
12	GNOMAD	ss4051322850	Apr 26, 2021 (155)
13	GNOMAD	ss4051322851	Apr 26, 2021 (155)
14	GNOMAD	ss4051322852	Apr 26, 2021 (155)
15	GNOMAD	ss4051322853	Apr 26, 2021 (155)
16	GNOMAD	ss4051322854	Apr 26, 2021 (155)
17	GNOMAD	ss4051322855	Apr 26, 2021 (155)
18	GNOMAD	ss4051322856	Apr 26, 2021 (155)
19	GNOMAD	ss4051322857	Apr 26, 2021 (155)
20	GNOMAD	ss4051322858	Apr 26, 2021 (155)
21	GNOMAD	ss4051322859	Apr 26, 2021 (155)
22	GNOMAD	ss4051322860	Apr 26, 2021 (155)
23	GNOMAD	ss4051322861	Apr 26, 2021 (155)
24	GNOMAD	ss4051322862	Apr 26, 2021 (155)
25	GNOMAD	ss4051322863	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5154021124	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5154021125	Apr 26, 2021 (155)
28	1000G_HIGH_COVERAGE	ss5250132867	Oct 12, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5250132868	Oct 12, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5250132869	Oct 12, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5250132870	Oct 12, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5250132871	Oct 12, 2022 (156)
33	HUGCELL_USP	ss5449932764	Oct 12, 2022 (156)
34	HUGCELL_USP	ss5449932765	Oct 12, 2022 (156)
35	TOMMO_GENOMICS	ss5684192389	Oct 12, 2022 (156)
36	TOMMO_GENOMICS	ss5684192390	Oct 12, 2022 (156)
37	TOMMO_GENOMICS	ss5684192391	Oct 12, 2022 (156)
38	TOMMO_GENOMICS	ss5684192393	Oct 12, 2022 (156)
39	YY_MCH	ss5802752738	Oct 12, 2022 (156)
40	EVA	ss5820850984	Oct 12, 2022 (156)
41	EVA	ss5820850985	Oct 12, 2022 (156)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 74731098 (NC_000002.12:135854529::A 121/46268) Row 74731099 (NC_000002.12:135854529::AA 3/46280) Row 74731100 (NC_000002.12:135854529::AAA 3/46278)...	-	Apr 26, 2021 (155)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 5414387 (NC_000002.12:135854535:A: 58/1804) Row 5414388 (NC_000002.12:135854534:AA: 7/1804) Row 5414389 (NC_000002.12:135854529:AAAAAAA: 17/1804)	-	Apr 25, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 5414387 (NC_000002.12:135854535:A: 58/1804) Row 5414388 (NC_000002.12:135854534:AA: 7/1804) Row 5414389 (NC_000002.12:135854529:AAAAAAA: 17/1804)	-	Apr 25, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 5414387 (NC_000002.12:135854535:A: 58/1804) Row 5414388 (NC_000002.12:135854534:AA: 7/1804) Row 5414389 (NC_000002.12:135854529:AAAAAAA: 17/1804)	-	Apr 25, 2020 (154)
61	8.3KJPN Submission ignored due to conflicting rows: Row 11990431 (NC_000002.11:136612099:AAAAAAA: 429/15656) Row 11990432 (NC_000002.11:136612099:A: 12/15656)	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 11990431 (NC_000002.11:136612099:AAAAAAA: 429/15656) Row 11990432 (NC_000002.11:136612099:A: 12/15656)	-	Apr 26, 2021 (155)
63	14KJPN Submission ignored due to conflicting rows: Row 18029493 (NC_000002.12:135854529::AAAA 15/23928) Row 18029494 (NC_000002.12:135854529:AAAAAAA: 827/23928) Row 18029495 (NC_000002.12:135854529::A 129/23928)...	-	Oct 12, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 18029493 (NC_000002.12:135854529::AAAA 15/23928) Row 18029494 (NC_000002.12:135854529:AAAAAAA: 827/23928) Row 18029495 (NC_000002.12:135854529::A 129/23928)...	-	Oct 12, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 18029493 (NC_000002.12:135854529::AAAA 15/23928) Row 18029494 (NC_000002.12:135854529:AAAAAAA: 827/23928) Row 18029495 (NC_000002.12:135854529::A 129/23928)...	-	Oct 12, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 18029493 (NC_000002.12:135854529::AAAA 15/23928) Row 18029494 (NC_000002.12:135854529:AAAAAAA: 827/23928) Row 18029495 (NC_000002.12:135854529::A 129/23928)...	-	Oct 12, 2022 (156)
67	ALFA	NC_000002.12 - 135854530	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
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4051322863	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4051322862	NC_000002.12:135854529:AAAAAAAAAAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4051322861	NC_000002.12:135854529:AAAAAAAAAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4051322860	NC_000002.12:135854529:AAAAAAAAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4051322859	NC_000002.12:135854529:AAAAAAAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5154021124	NC_000002.11:136612099:AAAAAAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3949036388, ss4051322858, ss5250132869, ss5449932765, ss5684192390, ss5802752738	NC_000002.12:135854529:AAAAAAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4051322857	NC_000002.12:135854529:AAAAAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4051322856, ss5250132871	NC_000002.12:135854529:AAAAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4051322855, ss5250132870	NC_000002.12:135854529:AAAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4051322854	NC_000002.12:135854529:AAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3704955035, ss4051322853	NC_000002.12:135854529:AA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3949036387	NC_000002.12:135854534:AA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5154021125	NC_000002.11:136612099:A:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4051322852, ss5250132868, ss5449932764, ss5684192393	NC_000002.12:135854529:A:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3704955034	NC_000002.12:135854530:A:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3949036386	NC_000002.12:135854535:A:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4051322848, ss5250132867, ss5684192391	NC_000002.12:135854529::A	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3704955033	NC_000002.12:135854531::A	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5820850985	NC_000002.11:136612099::AA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA
ss4051322849	NC_000002.12:135854529::AA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3704955032	NC_000002.12:135854531::AA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4051322850	NC_000002.12:135854529::AAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3704955031	NC_000002.12:135854531::AAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4051322851, ss5684192389	NC_000002.12:135854529::AAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
11186714824	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3704955030	NC_000002.12:135854531::AAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5820850984	NC_000002.11:136612099::AAAAA	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3323859679	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAA:	NC_000002.12:135854529:AAAAAAAAAAA… NC_000002.12:135854529:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA

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

No publications for rs1181597035

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

rs1181597035