Name: rs141869536
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.

rs141869536

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:70739503-70739527 (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(AC)₅ / del(AC)₄ / del(AC)₃ / d…
del(AC)₅ / del(AC)₄ / del(AC)₃ / delACAC / delAC / dupAC / dupACAC / dup(AC)₃ / dup(AC)₄ / dup(AC)₅ / dup(AC)₇ / dup(AC)₈ / dup(AC)₉
Variation Type: Indel Insertion and Deletion
Frequency: dupAC=0.4131 (2585/6258, ALFA)
dupAC=0.42 (17/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MAP3K9 : 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	6258	CACACACACACACACACACACACAC=0.5360	CACACACACACACAC=0.0000, CACACACACACACACAC=0.0000, CACACACACACACACACAC=0.0000, CACACACACACACACACACAC=0.0000, CACACACACACACACACACACAC=0.0051, CACACACACACACACACACACACACAC=0.4131, CACACACACACACACACACACACACACACACAC=0.0125, CACACACACACACACACACACACACACAC=0.0219, CACACACACACACACACACACACACACACAC=0.0115, CACACACACACACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACACACACACACACACACAC=0.0000	0.417287	0.266029	0.316684	32
European	Sub	5532	CACACACACACACACACACACACAC=0.4765	CACACACACACACAC=0.0000, CACACACACACACACAC=0.0000, CACACACACACACACACAC=0.0000, CACACACACACACACACACAC=0.0000, CACACACACACACACACACACAC=0.0056, CACACACACACACACACACACACACAC=0.4662, CACACACACACACACACACACACACACACACAC=0.0141, CACACACACACACACACACACACACACAC=0.0246, CACACACACACACACACACACACACACACAC=0.0130, CACACACACACACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACACACACACACACACAC=0.0000, CACACACACACACACACACACACACACACACACACACACACAC=0.0000	0.332792	0.303941	0.363267	32
African	Sub	530	CACACACACACACACACACACACAC=1.000	CACACACACACACAC=0.000, CACACACACACACACAC=0.000, CACACACACACACACACAC=0.000, CACACACACACACACACACAC=0.000, CACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACACACACACACACAC=0.000	1.0	0.0	0.0	N/A
African Others	Sub	12	CACACACACACACACACACACACAC=1.00	CACACACACACACAC=0.00, CACACACACACACACAC=0.00, CACACACACACACACACAC=0.00, CACACACACACACACACACAC=0.00, CACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
African American	Sub	518	CACACACACACACACACACACACAC=1.000	CACACACACACACAC=0.000, CACACACACACACACAC=0.000, CACACACACACACACACAC=0.000, CACACACACACACACACACAC=0.000, CACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACACACACACACAC=0.000, CACACACACACACACACACACACACACACACACACACACACAC=0.000	1.0	0.0	0.0	N/A
Asian	Sub	10	CACACACACACACACACACACACAC=1.0	CACACACACACACAC=0.0, CACACACACACACACAC=0.0, CACACACACACACACACAC=0.0, CACACACACACACACACACAC=0.0, CACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACACACACACAC=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	8	CACACACACACACACACACACACAC=1.0	CACACACACACACAC=0.0, CACACACACACACACAC=0.0, CACACACACACACACACAC=0.0, CACACACACACACACACACAC=0.0, CACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACACACACACAC=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	CACACACACACACACACACACACAC=1.0	CACACACACACACAC=0.0, CACACACACACACACAC=0.0, CACACACACACACACACAC=0.0, CACACACACACACACACACAC=0.0, CACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACACACACAC=0.0, CACACACACACACACACACACACACACACACACACACACACAC=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	32	CACACACACACACACACACACACAC=1.00	CACACACACACACAC=0.00, CACACACACACACACAC=0.00, CACACACACACACACACAC=0.00, CACACACACACACACACACAC=0.00, CACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	58	CACACACACACACACACACACACAC=1.00	CACACACACACACAC=0.00, CACACACACACACACAC=0.00, CACACACACACACACACAC=0.00, CACACACACACACACACACAC=0.00, CACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	24	CACACACACACACACACACACACAC=1.00	CACACACACACACAC=0.00, CACACACACACACACAC=0.00, CACACACACACACACACAC=0.00, CACACACACACACACACACAC=0.00, CACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACACACAC=0.00	1.0	0.0	0.0	N/A
Other	Sub	72	CACACACACACACACACACACACAC=0.89	CACACACACACACAC=0.00, CACACACACACACACAC=0.00, CACACACACACACACACAC=0.00, CACACACACACACACACACAC=0.00, CACACACACACACACACACACAC=0.01, CACACACACACACACACACACACACAC=0.08, CACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACAC=0.01, CACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACACAC=0.00, CACACACACACACACACACACACACACACACACACACACACAC=0.00	0.914286	0.085714	0.0	19

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	6258	(CA)₁₂C=0.5360	del(AC)₅=0.0000, del(AC)₄=0.0000, del(AC)₃=0.0000, delACAC=0.0000, delAC=0.0051, dupAC=0.4131, dupACAC=0.0219, dup(AC)₃=0.0115, dup(AC)₄=0.0125, dup(AC)₅=0.0000, dup(AC)₇=0.0000, dup(AC)₈=0.0000, dup(AC)₉=0.0000
Allele Frequency Aggregator	European	Sub	5532	(CA)₁₂C=0.4765	del(AC)₅=0.0000, del(AC)₄=0.0000, del(AC)₃=0.0000, delACAC=0.0000, delAC=0.0056, dupAC=0.4662, dupACAC=0.0246, dup(AC)₃=0.0130, dup(AC)₄=0.0141, dup(AC)₅=0.0000, dup(AC)₇=0.0000, dup(AC)₈=0.0000, dup(AC)₉=0.0000
Allele Frequency Aggregator	African	Sub	530	(CA)₁₂C=1.000	del(AC)₅=0.000, del(AC)₄=0.000, del(AC)₃=0.000, delACAC=0.000, delAC=0.000, dupAC=0.000, dupACAC=0.000, dup(AC)₃=0.000, dup(AC)₄=0.000, dup(AC)₅=0.000, dup(AC)₇=0.000, dup(AC)₈=0.000, dup(AC)₉=0.000
Allele Frequency Aggregator	Other	Sub	72	(CA)₁₂C=0.89	del(AC)₅=0.00, del(AC)₄=0.00, del(AC)₃=0.00, delACAC=0.00, delAC=0.01, dupAC=0.08, dupACAC=0.01, dup(AC)₃=0.00, dup(AC)₄=0.00, dup(AC)₅=0.00, dup(AC)₇=0.00, dup(AC)₈=0.00, dup(AC)₉=0.00
Allele Frequency Aggregator	Latin American 2	Sub	58	(CA)₁₂C=1.00	del(AC)₅=0.00, del(AC)₄=0.00, del(AC)₃=0.00, delACAC=0.00, delAC=0.00, dupAC=0.00, dupACAC=0.00, dup(AC)₃=0.00, dup(AC)₄=0.00, dup(AC)₅=0.00, dup(AC)₇=0.00, dup(AC)₈=0.00, dup(AC)₉=0.00
Allele Frequency Aggregator	Latin American 1	Sub	32	(CA)₁₂C=1.00	del(AC)₅=0.00, del(AC)₄=0.00, del(AC)₃=0.00, delACAC=0.00, delAC=0.00, dupAC=0.00, dupACAC=0.00, dup(AC)₃=0.00, dup(AC)₄=0.00, dup(AC)₅=0.00, dup(AC)₇=0.00, dup(AC)₈=0.00, dup(AC)₉=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(CA)₁₂C=1.00	del(AC)₅=0.00, del(AC)₄=0.00, del(AC)₃=0.00, delACAC=0.00, delAC=0.00, dupAC=0.00, dupACAC=0.00, dup(AC)₃=0.00, dup(AC)₄=0.00, dup(AC)₅=0.00, dup(AC)₇=0.00, dup(AC)₈=0.00, dup(AC)₉=0.00
Allele Frequency Aggregator	Asian	Sub	10	(CA)₁₂C=1.0	del(AC)₅=0.0, del(AC)₄=0.0, del(AC)₃=0.0, delACAC=0.0, delAC=0.0, dupAC=0.0, dupACAC=0.0, dup(AC)₃=0.0, dup(AC)₄=0.0, dup(AC)₅=0.0, dup(AC)₇=0.0, dup(AC)₈=0.0, dup(AC)₉=0.0
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupAC=0.42

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 14	NC_000014.9:g.70739504AC[7]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[8]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[9]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[10]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[11]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[13]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[14]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[15]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[16]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[17]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[19]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[20]
GRCh38.p14 chr 14	NC_000014.9:g.70739504AC[21]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[7]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[8]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[9]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[10]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[11]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[13]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[14]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[15]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[16]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[17]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[19]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[20]
GRCh37.p13 chr 14	NC_000014.8:g.71206221AC[21]

Gene: MAP3K9, mitogen-activated protein kinase kinase kinase 9 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MAP3K9 transcript variant 2	NM_001284230.2:c.1690+516… NM_001284230.2:c.1690+516TG[7]	N/A	Intron Variant
MAP3K9 transcript variant 3	NM_001284231.1:c.1045+372… NM_001284231.1:c.1045+372TG[7]	N/A	Intron Variant
MAP3K9 transcript variant 4	NM_001284232.1:c.916+372T… NM_001284232.1:c.916+372TG[7]	N/A	Intron Variant
MAP3K9 transcript variant 1	NM_033141.4:c.1690+516TG[… NM_033141.4:c.1690+516TG[7]	N/A	Intron Variant
MAP3K9 transcript variant X2	XM_005267683.6:c.1690+516… XM_005267683.6:c.1690+516TG[7]	N/A	Intron Variant
MAP3K9 transcript variant X1	XM_011536788.4:c.1834+372… XM_011536788.4:c.1834+372TG[7]	N/A	Intron Variant
MAP3K9 transcript variant X3	XM_011536792.1:c.916+372T… XM_011536792.1:c.916+372TG[7]	N/A	Intron Variant
MAP3K9 transcript variant X4	XM_011536794.3:c.748+372T… XM_011536794.3:c.748+372TG[7]	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	(CA)₁₂C=	del(AC)₅	del(AC)₄	del(AC)₃	delACAC	delAC	dupAC	dupACAC	dup(AC)₃	dup(AC)₄	dup(AC)₅	dup(AC)₇	dup(AC)₈	dup(AC)₉
GRCh38.p14 chr 14	NC_000014.9:g.70739503_70739527=	NC_000014.9:g.70739504AC[7]	NC_000014.9:g.70739504AC[8]	NC_000014.9:g.70739504AC[9]	NC_000014.9:g.70739504AC[10]	NC_000014.9:g.70739504AC[11]	NC_000014.9:g.70739504AC[13]	NC_000014.9:g.70739504AC[14]	NC_000014.9:g.70739504AC[15]	NC_000014.9:g.70739504AC[16]	NC_000014.9:g.70739504AC[17]	NC_000014.9:g.70739504AC[19]	NC_000014.9:g.70739504AC[20]	NC_000014.9:g.70739504AC[21]
GRCh37.p13 chr 14	NC_000014.8:g.71206220_71206244=	NC_000014.8:g.71206221AC[7]	NC_000014.8:g.71206221AC[8]	NC_000014.8:g.71206221AC[9]	NC_000014.8:g.71206221AC[10]	NC_000014.8:g.71206221AC[11]	NC_000014.8:g.71206221AC[13]	NC_000014.8:g.71206221AC[14]	NC_000014.8:g.71206221AC[15]	NC_000014.8:g.71206221AC[16]	NC_000014.8:g.71206221AC[17]	NC_000014.8:g.71206221AC[19]	NC_000014.8:g.71206221AC[20]	NC_000014.8:g.71206221AC[21]
MAP3K9 transcript variant 2	NM_001284230.2:c.1690+539=	NM_001284230.2:c.1690+516TG[7]	NM_001284230.2:c.1690+516TG[8]	NM_001284230.2:c.1690+516TG[9]	NM_001284230.2:c.1690+516TG[10]	NM_001284230.2:c.1690+516TG[11]	NM_001284230.2:c.1690+516TG[13]	NM_001284230.2:c.1690+516TG[14]	NM_001284230.2:c.1690+516TG[15]	NM_001284230.2:c.1690+516TG[16]	NM_001284230.2:c.1690+516TG[17]	NM_001284230.2:c.1690+516TG[19]	NM_001284230.2:c.1690+516TG[20]	NM_001284230.2:c.1690+516TG[21]
MAP3K9 transcript variant 3	NM_001284231.1:c.1045+395=	NM_001284231.1:c.1045+372TG[7]	NM_001284231.1:c.1045+372TG[8]	NM_001284231.1:c.1045+372TG[9]	NM_001284231.1:c.1045+372TG[10]	NM_001284231.1:c.1045+372TG[11]	NM_001284231.1:c.1045+372TG[13]	NM_001284231.1:c.1045+372TG[14]	NM_001284231.1:c.1045+372TG[15]	NM_001284231.1:c.1045+372TG[16]	NM_001284231.1:c.1045+372TG[17]	NM_001284231.1:c.1045+372TG[19]	NM_001284231.1:c.1045+372TG[20]	NM_001284231.1:c.1045+372TG[21]
MAP3K9 transcript variant 4	NM_001284232.1:c.916+395=	NM_001284232.1:c.916+372TG[7]	NM_001284232.1:c.916+372TG[8]	NM_001284232.1:c.916+372TG[9]	NM_001284232.1:c.916+372TG[10]	NM_001284232.1:c.916+372TG[11]	NM_001284232.1:c.916+372TG[13]	NM_001284232.1:c.916+372TG[14]	NM_001284232.1:c.916+372TG[15]	NM_001284232.1:c.916+372TG[16]	NM_001284232.1:c.916+372TG[17]	NM_001284232.1:c.916+372TG[19]	NM_001284232.1:c.916+372TG[20]	NM_001284232.1:c.916+372TG[21]
MAP3K9 transcript	NM_033141.2:c.1690+539=	NM_033141.2:c.1690+516TG[7]	NM_033141.2:c.1690+516TG[8]	NM_033141.2:c.1690+516TG[9]	NM_033141.2:c.1690+516TG[10]	NM_033141.2:c.1690+516TG[11]	NM_033141.2:c.1690+516TG[13]	NM_033141.2:c.1690+516TG[14]	NM_033141.2:c.1690+516TG[15]	NM_033141.2:c.1690+516TG[16]	NM_033141.2:c.1690+516TG[17]	NM_033141.2:c.1690+516TG[19]	NM_033141.2:c.1690+516TG[20]	NM_033141.2:c.1690+516TG[21]
MAP3K9 transcript variant 1	NM_033141.4:c.1690+539=	NM_033141.4:c.1690+516TG[7]	NM_033141.4:c.1690+516TG[8]	NM_033141.4:c.1690+516TG[9]	NM_033141.4:c.1690+516TG[10]	NM_033141.4:c.1690+516TG[11]	NM_033141.4:c.1690+516TG[13]	NM_033141.4:c.1690+516TG[14]	NM_033141.4:c.1690+516TG[15]	NM_033141.4:c.1690+516TG[16]	NM_033141.4:c.1690+516TG[17]	NM_033141.4:c.1690+516TG[19]	NM_033141.4:c.1690+516TG[20]	NM_033141.4:c.1690+516TG[21]
MAP3K9 transcript variant X1	XM_005267682.1:c.1690+539=	XM_005267682.1:c.1690+516TG[7]	XM_005267682.1:c.1690+516TG[8]	XM_005267682.1:c.1690+516TG[9]	XM_005267682.1:c.1690+516TG[10]	XM_005267682.1:c.1690+516TG[11]	XM_005267682.1:c.1690+516TG[13]	XM_005267682.1:c.1690+516TG[14]	XM_005267682.1:c.1690+516TG[15]	XM_005267682.1:c.1690+516TG[16]	XM_005267682.1:c.1690+516TG[17]	XM_005267682.1:c.1690+516TG[19]	XM_005267682.1:c.1690+516TG[20]	XM_005267682.1:c.1690+516TG[21]
MAP3K9 transcript variant X2	XM_005267683.1:c.1690+539=	XM_005267683.1:c.1690+516TG[7]	XM_005267683.1:c.1690+516TG[8]	XM_005267683.1:c.1690+516TG[9]	XM_005267683.1:c.1690+516TG[10]	XM_005267683.1:c.1690+516TG[11]	XM_005267683.1:c.1690+516TG[13]	XM_005267683.1:c.1690+516TG[14]	XM_005267683.1:c.1690+516TG[15]	XM_005267683.1:c.1690+516TG[16]	XM_005267683.1:c.1690+516TG[17]	XM_005267683.1:c.1690+516TG[19]	XM_005267683.1:c.1690+516TG[20]	XM_005267683.1:c.1690+516TG[21]
MAP3K9 transcript variant X2	XM_005267683.6:c.1690+539=	XM_005267683.6:c.1690+516TG[7]	XM_005267683.6:c.1690+516TG[8]	XM_005267683.6:c.1690+516TG[9]	XM_005267683.6:c.1690+516TG[10]	XM_005267683.6:c.1690+516TG[11]	XM_005267683.6:c.1690+516TG[13]	XM_005267683.6:c.1690+516TG[14]	XM_005267683.6:c.1690+516TG[15]	XM_005267683.6:c.1690+516TG[16]	XM_005267683.6:c.1690+516TG[17]	XM_005267683.6:c.1690+516TG[19]	XM_005267683.6:c.1690+516TG[20]	XM_005267683.6:c.1690+516TG[21]
MAP3K9 transcript variant X3	XM_005267684.1:c.916+395=	XM_005267684.1:c.916+372TG[7]	XM_005267684.1:c.916+372TG[8]	XM_005267684.1:c.916+372TG[9]	XM_005267684.1:c.916+372TG[10]	XM_005267684.1:c.916+372TG[11]	XM_005267684.1:c.916+372TG[13]	XM_005267684.1:c.916+372TG[14]	XM_005267684.1:c.916+372TG[15]	XM_005267684.1:c.916+372TG[16]	XM_005267684.1:c.916+372TG[17]	XM_005267684.1:c.916+372TG[19]	XM_005267684.1:c.916+372TG[20]	XM_005267684.1:c.916+372TG[21]
MAP3K9 transcript variant X4	XM_005267685.1:c.901+539=	XM_005267685.1:c.901+516TG[7]	XM_005267685.1:c.901+516TG[8]	XM_005267685.1:c.901+516TG[9]	XM_005267685.1:c.901+516TG[10]	XM_005267685.1:c.901+516TG[11]	XM_005267685.1:c.901+516TG[13]	XM_005267685.1:c.901+516TG[14]	XM_005267685.1:c.901+516TG[15]	XM_005267685.1:c.901+516TG[16]	XM_005267685.1:c.901+516TG[17]	XM_005267685.1:c.901+516TG[19]	XM_005267685.1:c.901+516TG[20]	XM_005267685.1:c.901+516TG[21]
MAP3K9 transcript variant X1	XM_011536788.4:c.1834+395=	XM_011536788.4:c.1834+372TG[7]	XM_011536788.4:c.1834+372TG[8]	XM_011536788.4:c.1834+372TG[9]	XM_011536788.4:c.1834+372TG[10]	XM_011536788.4:c.1834+372TG[11]	XM_011536788.4:c.1834+372TG[13]	XM_011536788.4:c.1834+372TG[14]	XM_011536788.4:c.1834+372TG[15]	XM_011536788.4:c.1834+372TG[16]	XM_011536788.4:c.1834+372TG[17]	XM_011536788.4:c.1834+372TG[19]	XM_011536788.4:c.1834+372TG[20]	XM_011536788.4:c.1834+372TG[21]
MAP3K9 transcript variant X3	XM_011536792.1:c.916+395=	XM_011536792.1:c.916+372TG[7]	XM_011536792.1:c.916+372TG[8]	XM_011536792.1:c.916+372TG[9]	XM_011536792.1:c.916+372TG[10]	XM_011536792.1:c.916+372TG[11]	XM_011536792.1:c.916+372TG[13]	XM_011536792.1:c.916+372TG[14]	XM_011536792.1:c.916+372TG[15]	XM_011536792.1:c.916+372TG[16]	XM_011536792.1:c.916+372TG[17]	XM_011536792.1:c.916+372TG[19]	XM_011536792.1:c.916+372TG[20]	XM_011536792.1:c.916+372TG[21]
MAP3K9 transcript variant X4	XM_011536794.3:c.748+395=	XM_011536794.3:c.748+372TG[7]	XM_011536794.3:c.748+372TG[8]	XM_011536794.3:c.748+372TG[9]	XM_011536794.3:c.748+372TG[10]	XM_011536794.3:c.748+372TG[11]	XM_011536794.3:c.748+372TG[13]	XM_011536794.3:c.748+372TG[14]	XM_011536794.3:c.748+372TG[15]	XM_011536794.3:c.748+372TG[16]	XM_011536794.3:c.748+372TG[17]	XM_011536794.3:c.748+372TG[19]	XM_011536794.3:c.748+372TG[20]	XM_011536794.3:c.748+372TG[21]

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#.

77 SubSNP, 39 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81698070	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss95644741	Dec 05, 2013 (138)
3	GMI	ss287920181	Dec 06, 2013 (138)
4	GMI	ss289228841	Oct 12, 2018 (152)
5	1000GENOMES	ss327617594	May 09, 2011 (134)
6	1000GENOMES	ss327730934	May 09, 2011 (134)
7	1000GENOMES	ss328139800	May 09, 2011 (134)
8	LUNTER	ss552372254	Apr 25, 2013 (138)
9	LUNTER	ss552703605	Apr 25, 2013 (138)
10	LUNTER	ss553554085	Apr 25, 2013 (138)
11	SSMP	ss664240651	Apr 01, 2015 (144)
12	BILGI_BIOE	ss666631239	Apr 25, 2013 (138)
13	1000GENOMES	ss1374248852	Aug 21, 2014 (142)
14	1000GENOMES	ss1374248856	Aug 21, 2014 (142)
15	1000GENOMES	ss1374248864	Aug 21, 2014 (142)
16	DDI	ss1536789321	Apr 01, 2015 (144)
17	EVA_GENOME_DK	ss1574779841	Apr 01, 2015 (144)
18	EVA_UK10K_ALSPAC	ss1708109388	Apr 01, 2015 (144)
19	EVA_UK10K_ALSPAC	ss1708109390	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1708109410	Apr 01, 2015 (144)
21	EVA_UK10K_TWINSUK	ss1708109413	Apr 01, 2015 (144)
22	SWEGEN	ss3012416336	Nov 17, 2017 (151)
23	MCHAISSO	ss3064633766	Nov 08, 2017 (151)
24	MCHAISSO	ss3065562826	Nov 17, 2017 (151)
25	URBANLAB	ss3650232864	Oct 12, 2018 (152)
26	ACPOP	ss3740498509	Jul 13, 2019 (153)
27	ACPOP	ss3740498510	Jul 13, 2019 (153)
28	ACPOP	ss3740498511	Jul 13, 2019 (153)
29	ACPOP	ss3740498512	Jul 13, 2019 (153)
30	ACPOP	ss3740498513	Jul 13, 2019 (153)
31	PACBIO	ss3787701952	Jul 13, 2019 (153)
32	PACBIO	ss3792734367	Jul 13, 2019 (153)
33	PACBIO	ss3797618686	Jul 13, 2019 (153)
34	KHV_HUMAN_GENOMES	ss3817814287	Jul 13, 2019 (153)
35	KHV_HUMAN_GENOMES	ss3817814288	Jul 13, 2019 (153)
36	KHV_HUMAN_GENOMES	ss3817814290	Jul 13, 2019 (153)
37	EVA	ss3833987039	Apr 27, 2020 (154)
38	KOGIC	ss3975191759	Apr 27, 2020 (154)
39	KOGIC	ss3975191760	Apr 27, 2020 (154)
40	KOGIC	ss3975191761	Apr 27, 2020 (154)
41	KOGIC	ss3975191762	Apr 27, 2020 (154)
42	GNOMAD	ss4280333469	Apr 27, 2021 (155)
43	GNOMAD	ss4280333470	Apr 27, 2021 (155)
44	GNOMAD	ss4280333471	Apr 27, 2021 (155)
45	GNOMAD	ss4280333472	Apr 27, 2021 (155)
46	GNOMAD	ss4280333473	Apr 27, 2021 (155)
47	GNOMAD	ss4280333474	Apr 27, 2021 (155)
48	GNOMAD	ss4280333475	Apr 27, 2021 (155)
49	GNOMAD	ss4280333476	Apr 27, 2021 (155)
50	GNOMAD	ss4280333477	Apr 27, 2021 (155)
51	GNOMAD	ss4280333478	Apr 27, 2021 (155)
52	GNOMAD	ss4280333479	Apr 27, 2021 (155)
53	TOMMO_GENOMICS	ss5213828174	Apr 27, 2021 (155)
54	TOMMO_GENOMICS	ss5213828175	Apr 27, 2021 (155)
55	TOMMO_GENOMICS	ss5213828176	Apr 27, 2021 (155)
56	TOMMO_GENOMICS	ss5213828177	Apr 27, 2021 (155)
57	TOMMO_GENOMICS	ss5213828178	Apr 27, 2021 (155)
58	1000G_HIGH_COVERAGE	ss5296685813	Oct 16, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5296685814	Oct 16, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5296685815	Oct 16, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5296685816	Oct 16, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5296685817	Oct 16, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5296685818	Oct 16, 2022 (156)
64	HUGCELL_USP	ss5490684112	Oct 16, 2022 (156)
65	HUGCELL_USP	ss5490684113	Oct 16, 2022 (156)
66	HUGCELL_USP	ss5490684114	Oct 16, 2022 (156)
67	HUGCELL_USP	ss5490684115	Oct 16, 2022 (156)
68	HUGCELL_USP	ss5490684116	Oct 16, 2022 (156)
69	HUGCELL_USP	ss5490684117	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5766802969	Oct 16, 2022 (156)
71	TOMMO_GENOMICS	ss5766802970	Oct 16, 2022 (156)
72	TOMMO_GENOMICS	ss5766802971	Oct 16, 2022 (156)
73	TOMMO_GENOMICS	ss5766802972	Oct 16, 2022 (156)
74	TOMMO_GENOMICS	ss5766802973	Oct 16, 2022 (156)
75	EVA	ss5841291966	Oct 16, 2022 (156)
76	EVA	ss5841291967	Oct 16, 2022 (156)
77	EVA	ss5851090229	Oct 16, 2022 (156)
78	1000Genomes Submission ignored due to conflicting rows: Row 64532622 (NC_000014.8:71206219::CA 2225/5008) Row 64532623 (NC_000014.8:71206219::CACACA 78/5008) Row 64532625 (NC_000014.8:71206242::ACAC 329/5008)	-	Oct 12, 2018 (152)
79	1000Genomes Submission ignored due to conflicting rows: Row 64532622 (NC_000014.8:71206219::CA 2225/5008) Row 64532623 (NC_000014.8:71206219::CACACA 78/5008) Row 64532625 (NC_000014.8:71206242::ACAC 329/5008)	-	Oct 12, 2018 (152)
80	1000Genomes Submission ignored due to conflicting rows: Row 64532622 (NC_000014.8:71206219::CA 2225/5008) Row 64532623 (NC_000014.8:71206219::CACACA 78/5008) Row 64532625 (NC_000014.8:71206242::ACAC 329/5008)	-	Oct 12, 2018 (152)
81	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 35857550 (NC_000014.8:71206219::CA 2016/3854) Row 35857551 (NC_000014.8:71206219::CACA 182/3854)	-	Oct 12, 2018 (152)
82	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 35857550 (NC_000014.8:71206219::CA 2016/3854) Row 35857551 (NC_000014.8:71206219::CACA 182/3854)	-	Oct 12, 2018 (152)
83	The Danish reference pan genome	NC_000014.8 - 71206220	Apr 27, 2020 (154)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455006490 (NC_000014.9:70739502::CA 68035/136496) Row 455006491 (NC_000014.9:70739502::CACA 9462/136574) Row 455006492 (NC_000014.9:70739502::CACACA 3100/136630)...	-	Apr 27, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455006490 (NC_000014.9:70739502::CA 68035/136496) Row 455006491 (NC_000014.9:70739502::CACA 9462/136574) Row 455006492 (NC_000014.9:70739502::CACACA 3100/136630)...	-	Apr 27, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455006490 (NC_000014.9:70739502::CA 68035/136496) Row 455006491 (NC_000014.9:70739502::CACA 9462/136574) Row 455006492 (NC_000014.9:70739502::CACACA 3100/136630)...	-	Apr 27, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455006490 (NC_000014.9:70739502::CA 68035/136496) Row 455006491 (NC_000014.9:70739502::CACA 9462/136574) Row 455006492 (NC_000014.9:70739502::CACACA 3100/136630)...	-	Apr 27, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455006490 (NC_000014.9:70739502::CA 68035/136496) Row 455006491 (NC_000014.9:70739502::CACA 9462/136574) Row 455006492 (NC_000014.9:70739502::CACACA 3100/136630)...	-	Apr 27, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455006490 (NC_000014.9:70739502::CA 68035/136496) Row 455006491 (NC_000014.9:70739502::CACA 9462/136574) Row 455006492 (NC_000014.9:70739502::CACACA 3100/136630)...	-	Apr 27, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455006490 (NC_000014.9:70739502::CA 68035/136496) Row 455006491 (NC_000014.9:70739502::CACA 9462/136574) Row 455006492 (NC_000014.9:70739502::CACACA 3100/136630)...	-	Apr 27, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455006490 (NC_000014.9:70739502::CA 68035/136496) Row 455006491 (NC_000014.9:70739502::CACA 9462/136574) Row 455006492 (NC_000014.9:70739502::CACACA 3100/136630)...	-	Apr 27, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455006490 (NC_000014.9:70739502::CA 68035/136496) Row 455006491 (NC_000014.9:70739502::CACA 9462/136574) Row 455006492 (NC_000014.9:70739502::CACACA 3100/136630)...	-	Apr 27, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455006490 (NC_000014.9:70739502::CA 68035/136496) Row 455006491 (NC_000014.9:70739502::CACA 9462/136574) Row 455006492 (NC_000014.9:70739502::CACACA 3100/136630)...	-	Apr 27, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455006490 (NC_000014.9:70739502::CA 68035/136496) Row 455006491 (NC_000014.9:70739502::CACA 9462/136574) Row 455006492 (NC_000014.9:70739502::CACACA 3100/136630)...	-	Apr 27, 2021 (155)
95	Korean Genome Project Submission ignored due to conflicting rows: Row 31569760 (NC_000014.9:70739504::CA 1131/1832) Row 31569761 (NC_000014.9:70739502:CA: 76/1832) Row 31569762 (NC_000014.9:70739504::CACA 53/1832)...	-	Apr 27, 2020 (154)
96	Korean Genome Project Submission ignored due to conflicting rows: Row 31569760 (NC_000014.9:70739504::CA 1131/1832) Row 31569761 (NC_000014.9:70739502:CA: 76/1832) Row 31569762 (NC_000014.9:70739504::CACA 53/1832)...	-	Apr 27, 2020 (154)
97	Korean Genome Project Submission ignored due to conflicting rows: Row 31569760 (NC_000014.9:70739504::CA 1131/1832) Row 31569761 (NC_000014.9:70739502:CA: 76/1832) Row 31569762 (NC_000014.9:70739504::CACA 53/1832)...	-	Apr 27, 2020 (154)
98	Korean Genome Project Submission ignored due to conflicting rows: Row 31569760 (NC_000014.9:70739504::CA 1131/1832) Row 31569761 (NC_000014.9:70739502:CA: 76/1832) Row 31569762 (NC_000014.9:70739504::CACA 53/1832)...	-	Apr 27, 2020 (154)
99	Northern Sweden Submission ignored due to conflicting rows: Row 13783374 (NC_000014.8:71206219::CA 332/600) Row 13783375 (NC_000014.8:71206219:CA: 14/600) Row 13783376 (NC_000014.8:71206219::CACA 23/600)...	-	Jul 13, 2019 (153)
100	Northern Sweden Submission ignored due to conflicting rows: Row 13783374 (NC_000014.8:71206219::CA 332/600) Row 13783375 (NC_000014.8:71206219:CA: 14/600) Row 13783376 (NC_000014.8:71206219::CACA 23/600)...	-	Jul 13, 2019 (153)
101	Northern Sweden Submission ignored due to conflicting rows: Row 13783374 (NC_000014.8:71206219::CA 332/600) Row 13783375 (NC_000014.8:71206219:CA: 14/600) Row 13783376 (NC_000014.8:71206219::CACA 23/600)...	-	Jul 13, 2019 (153)
102	Northern Sweden Submission ignored due to conflicting rows: Row 13783374 (NC_000014.8:71206219::CA 332/600) Row 13783375 (NC_000014.8:71206219:CA: 14/600) Row 13783376 (NC_000014.8:71206219::CACA 23/600)...	-	Jul 13, 2019 (153)
103	Northern Sweden Submission ignored due to conflicting rows: Row 13783374 (NC_000014.8:71206219::CA 332/600) Row 13783375 (NC_000014.8:71206219:CA: 14/600) Row 13783376 (NC_000014.8:71206219::CACA 23/600)...	-	Jul 13, 2019 (153)
104	8.3KJPN Submission ignored due to conflicting rows: Row 71797481 (NC_000014.8:71206219::CA 10264/16760) Row 71797482 (NC_000014.8:71206219:CA: 800/16760) Row 71797483 (NC_000014.8:71206219::CACA 379/16760)...	-	Apr 27, 2021 (155)
105	8.3KJPN Submission ignored due to conflicting rows: Row 71797481 (NC_000014.8:71206219::CA 10264/16760) Row 71797482 (NC_000014.8:71206219:CA: 800/16760) Row 71797483 (NC_000014.8:71206219::CACA 379/16760)...	-	Apr 27, 2021 (155)
106	8.3KJPN Submission ignored due to conflicting rows: Row 71797481 (NC_000014.8:71206219::CA 10264/16760) Row 71797482 (NC_000014.8:71206219:CA: 800/16760) Row 71797483 (NC_000014.8:71206219::CACA 379/16760)...	-	Apr 27, 2021 (155)
107	8.3KJPN Submission ignored due to conflicting rows: Row 71797481 (NC_000014.8:71206219::CA 10264/16760) Row 71797482 (NC_000014.8:71206219:CA: 800/16760) Row 71797483 (NC_000014.8:71206219::CACA 379/16760)...	-	Apr 27, 2021 (155)
108	8.3KJPN Submission ignored due to conflicting rows: Row 71797481 (NC_000014.8:71206219::CA 10264/16760) Row 71797482 (NC_000014.8:71206219:CA: 800/16760) Row 71797483 (NC_000014.8:71206219::CACA 379/16760)...	-	Apr 27, 2021 (155)
109	14KJPN Submission ignored due to conflicting rows: Row 100640073 (NC_000014.9:70739502::CA 17335/28258) Row 100640074 (NC_000014.9:70739502::CACA 612/28258) Row 100640075 (NC_000014.9:70739502:CA: 1368/28258)...	-	Oct 16, 2022 (156)
110	14KJPN Submission ignored due to conflicting rows: Row 100640073 (NC_000014.9:70739502::CA 17335/28258) Row 100640074 (NC_000014.9:70739502::CACA 612/28258) Row 100640075 (NC_000014.9:70739502:CA: 1368/28258)...	-	Oct 16, 2022 (156)
111	14KJPN Submission ignored due to conflicting rows: Row 100640073 (NC_000014.9:70739502::CA 17335/28258) Row 100640074 (NC_000014.9:70739502::CACA 612/28258) Row 100640075 (NC_000014.9:70739502:CA: 1368/28258)...	-	Oct 16, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 100640073 (NC_000014.9:70739502::CA 17335/28258) Row 100640074 (NC_000014.9:70739502::CACA 612/28258) Row 100640075 (NC_000014.9:70739502:CA: 1368/28258)...	-	Oct 16, 2022 (156)
113	14KJPN Submission ignored due to conflicting rows: Row 100640073 (NC_000014.9:70739502::CA 17335/28258) Row 100640074 (NC_000014.9:70739502::CACA 612/28258) Row 100640075 (NC_000014.9:70739502:CA: 1368/28258)...	-	Oct 16, 2022 (156)
114	UK 10K study - Twins Submission ignored due to conflicting rows: Row 35857550 (NC_000014.8:71206219::CA 1990/3708) Row 35857551 (NC_000014.8:71206219::CACA 163/3708)	-	Oct 12, 2018 (152)
115	UK 10K study - Twins Submission ignored due to conflicting rows: Row 35857550 (NC_000014.8:71206219::CA 1990/3708) Row 35857551 (NC_000014.8:71206219::CACA 163/3708)	-	Oct 12, 2018 (152)
116	ALFA	NC_000014.9 - 70739503	Apr 27, 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
ss4280333479	NC_000014.9:70739502:CACACACACA:	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACAC	(self)
ss5213828178	NC_000014.8:71206219:CACACA:	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACAC	(self)
ss4280333478, ss5766802973	NC_000014.9:70739502:CACACA:	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACAC	(self)
ss4280333477, ss5490684116	NC_000014.9:70739502:CACA:	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACAC	(self)
ss3012416336, ss3740498510, ss3833987039, ss5213828175	NC_000014.8:71206219:CA:	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACAC	(self)
ss3065562826, ss3975191760, ss4280333476, ss5296685814, ss5490684114, ss5766802971	NC_000014.9:70739502:CA:	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACAC	(self)
ss327617594, ss327730934, ss328139800, ss552372254, ss552703605, ss553554085	NC_000014.7:70275972::CA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
ss289228841	NC_000014.7:70275997::AC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
459210, ss664240651, ss666631239, ss1374248852, ss1536789321, ss1574779841, ss1708109388, ss1708109410, ss3740498509, ss3787701952, ss3792734367, ss3797618686, ss5213828174, ss5841291966	NC_000014.8:71206219::CA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
ss3064633766, ss3817814287, ss4280333469, ss5296685815, ss5490684113, ss5766802969, ss5851090229	NC_000014.9:70739502::CA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
ss3975191759	NC_000014.9:70739504::CA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
ss3650232864	NC_000014.9:70739527::AC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
ss81698070, ss95644741, ss287920181	NT_026437.12:52206244::AC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACAC	(self)
ss1708109390, ss1708109413, ss3740498511, ss5213828176	NC_000014.8:71206219::CACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC	(self)
ss1374248864	NC_000014.8:71206242::ACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC	(self)
ss4280333470, ss5296685813, ss5490684112, ss5766802970	NC_000014.9:70739502::CACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC	(self)
ss3975191761	NC_000014.9:70739504::CACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC	(self)
ss3817814290	NC_000014.9:70739525::ACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC	(self)
ss1374248856, ss3740498512, ss5213828177, ss5841291967	NC_000014.8:71206219::CACACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC	(self)
ss3817814288, ss4280333471, ss5296685816, ss5490684115, ss5766802972	NC_000014.9:70739502::CACACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC	(self)
ss3975191762	NC_000014.9:70739504::CACACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC	(self)
ss3740498513	NC_000014.8:71206219::CACACACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC	(self)
ss4280333472, ss5296685817, ss5490684117	NC_000014.9:70739502::CACACACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC	(self)
ss4280333473	NC_000014.9:70739502::CACACACACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC	(self)
ss4280333474	NC_000014.9:70739502::CACACACACACA… NC_000014.9:70739502::CACACACACACACACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC	(self)
ss4280333475, ss5296685818	NC_000014.9:70739502::CACACACACACA… NC_000014.9:70739502::CACACACACACACACACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC	(self)
8311071687	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3214642331	NC_000014.9:70739502::CACACACACACA… NC_000014.9:70739502::CACACACACACACA	NC_000014.9:70739502:CACACACACACAC… NC_000014.9:70739502:CACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC

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

No publications for rs141869536

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

rs141869536