Name: rs1177241176
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.

rs1177241176

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:110268611-110268627 (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)₁₂ / del(A)₈ / del(A)₇ / del…
del(A)₁₂ / 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 / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₀ / dup(A)₁₁ / dup(A)₁₂ / ins(A)₁₉ / ins(A)₂₁
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₇=0.000215 (57/264690, TOPMED)
del(A)₁₂=0.0000 (0/5338, ALFA)
del(A)₈=0.0000 (0/5338, ALFA) (+ 11 more)
del(A)₇=0.0000 (0/5338, ALFA)
del(A)₆=0.0000 (0/5338, ALFA)
del(A)₅=0.0000 (0/5338, ALFA)
del(A)₄=0.0000 (0/5338, ALFA)
delAAA=0.0000 (0/5338, ALFA)
delAA=0.0000 (0/5338, ALFA)
delA=0.0000 (0/5338, ALFA)
dupA=0.0000 (0/5338, ALFA)
dupAA=0.0000 (0/5338, ALFA)
dupAAA=0.0000 (0/5338, ALFA)
dup(A)₅=0.0000 (0/5338, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KCNC4 : 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	5338	AAAAAAAAAAAAAAAAA=1.0000	AAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	3782	AAAAAAAAAAAAAAAAA=1.0000	AAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	998	AAAAAAAAAAAAAAAAA=1.000	AAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	44	AAAAAAAAAAAAAAAAA=1.00	AAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	954	AAAAAAAAAAAAAAAAA=1.000	AAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	48	AAAAAAAAAAAAAAAAA=1.00	AAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	40	AAAAAAAAAAAAAAAAA=1.00	AAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	8	AAAAAAAAAAAAAAAAA=1.0	AAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	62	AAAAAAAAAAAAAAAAA=1.00	AAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	226	AAAAAAAAAAAAAAAAA=1.000	AAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	32	AAAAAAAAAAAAAAAAA=1.00	AAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	190	AAAAAAAAAAAAAAAAA=1.000	AAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(A)₁₇=0.999785	del(A)₇=0.000215
Allele Frequency Aggregator	Total	Global	5338	(A)₁₇=1.0000	del(A)₁₂=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	3782	(A)₁₇=1.0000	del(A)₁₂=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	African	Sub	998	(A)₁₇=1.000	del(A)₁₂=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	226	(A)₁₇=1.000	del(A)₁₂=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	190	(A)₁₇=1.000	del(A)₁₂=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	62	(A)₁₇=1.00	del(A)₁₂=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Asian	Sub	48	(A)₁₇=1.00	del(A)₁₂=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	32	(A)₁₇=1.00	del(A)₁₂=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=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 1	NC_000001.11:g.110268616_110268627del
GRCh38.p14 chr 1	NC_000001.11:g.110268620_110268627del
GRCh38.p14 chr 1	NC_000001.11:g.110268621_110268627del
GRCh38.p14 chr 1	NC_000001.11:g.110268622_110268627del
GRCh38.p14 chr 1	NC_000001.11:g.110268623_110268627del
GRCh38.p14 chr 1	NC_000001.11:g.110268624_110268627del
GRCh38.p14 chr 1	NC_000001.11:g.110268625_110268627del
GRCh38.p14 chr 1	NC_000001.11:g.110268626_110268627del
GRCh38.p14 chr 1	NC_000001.11:g.110268627del
GRCh38.p14 chr 1	NC_000001.11:g.110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268626_110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268625_110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268624_110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268623_110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268622_110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268621_110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268620_110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268619_110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268618_110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268617_110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268616_110268627dup
GRCh38.p14 chr 1	NC_000001.11:g.110268627_110268628insAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 1	NC_000001.11:g.110268627_110268628insAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 1	NC_000001.10:g.110811238_110811249del
GRCh37.p13 chr 1	NC_000001.10:g.110811242_110811249del
GRCh37.p13 chr 1	NC_000001.10:g.110811243_110811249del
GRCh37.p13 chr 1	NC_000001.10:g.110811244_110811249del
GRCh37.p13 chr 1	NC_000001.10:g.110811245_110811249del
GRCh37.p13 chr 1	NC_000001.10:g.110811246_110811249del
GRCh37.p13 chr 1	NC_000001.10:g.110811247_110811249del
GRCh37.p13 chr 1	NC_000001.10:g.110811248_110811249del
GRCh37.p13 chr 1	NC_000001.10:g.110811249del
GRCh37.p13 chr 1	NC_000001.10:g.110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811248_110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811247_110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811246_110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811245_110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811244_110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811243_110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811242_110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811241_110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811240_110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811239_110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811238_110811249dup
GRCh37.p13 chr 1	NC_000001.10:g.110811249_110811250insAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 1	NC_000001.10:g.110811249_110811250insAAAAAAAAAAAAAAAAAAAAA

Gene: KCNC4, potassium voltage-gated channel subfamily C member 4 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KCNC4 transcript variant 3	NM_001039574.3:c.	N/A	Genic Downstream Transcript Variant
KCNC4 transcript variant 5	NM_001377330.1:c.	N/A	Genic Downstream Transcript Variant
KCNC4 transcript variant 6	NM_001377331.1:c.	N/A	Genic Downstream Transcript Variant
KCNC4 transcript variant 1	NM_004978.6:c.	N/A	Genic Downstream Transcript Variant
KCNC4 transcript variant 4	NR_036437.2:n.	N/A	Genic Downstream Transcript Variant
KCNC4 transcript variant X1	XM_006710625.5:c.1820-139… XM_006710625.5:c.1820-13918_1820-13907del	N/A	Intron Variant
KCNC4 transcript variant X3	XM_047419679.1:c.883-1391… XM_047419679.1:c.883-13918_883-13907del	N/A	Intron Variant
KCNC4 transcript variant X2	XM_011541401.4:c.	N/A	Genic Downstream Transcript Variant
KCNC4 transcript variant X4	XM_011541404.3:c.	N/A	Genic Downstream Transcript Variant
KCNC4 transcript variant X6	XM_024446790.2:c.	N/A	Genic Downstream Transcript Variant
KCNC4 transcript variant X5	XM_047419680.1:c.	N/A	Genic Downstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(A)₁₇=	del(A)₁₂	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	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₀	dup(A)₁₁	dup(A)₁₂	ins(A)₁₉	ins(A)₂₁
GRCh38.p14 chr 1	NC_000001.11:g.110268611_110268627=	NC_000001.11:g.110268616_110268627del	NC_000001.11:g.110268620_110268627del	NC_000001.11:g.110268621_110268627del	NC_000001.11:g.110268622_110268627del	NC_000001.11:g.110268623_110268627del	NC_000001.11:g.110268624_110268627del	NC_000001.11:g.110268625_110268627del	NC_000001.11:g.110268626_110268627del	NC_000001.11:g.110268627del	NC_000001.11:g.110268627dup	NC_000001.11:g.110268626_110268627dup	NC_000001.11:g.110268625_110268627dup	NC_000001.11:g.110268624_110268627dup	NC_000001.11:g.110268623_110268627dup	NC_000001.11:g.110268622_110268627dup	NC_000001.11:g.110268621_110268627dup	NC_000001.11:g.110268620_110268627dup	NC_000001.11:g.110268619_110268627dup	NC_000001.11:g.110268618_110268627dup	NC_000001.11:g.110268617_110268627dup	NC_000001.11:g.110268616_110268627dup	NC_000001.11:g.110268627_110268628insAAAAAAAAAAAAAAAAAAA	NC_000001.11:g.110268627_110268628insAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 1	NC_000001.10:g.110811233_110811249=	NC_000001.10:g.110811238_110811249del	NC_000001.10:g.110811242_110811249del	NC_000001.10:g.110811243_110811249del	NC_000001.10:g.110811244_110811249del	NC_000001.10:g.110811245_110811249del	NC_000001.10:g.110811246_110811249del	NC_000001.10:g.110811247_110811249del	NC_000001.10:g.110811248_110811249del	NC_000001.10:g.110811249del	NC_000001.10:g.110811249dup	NC_000001.10:g.110811248_110811249dup	NC_000001.10:g.110811247_110811249dup	NC_000001.10:g.110811246_110811249dup	NC_000001.10:g.110811245_110811249dup	NC_000001.10:g.110811244_110811249dup	NC_000001.10:g.110811243_110811249dup	NC_000001.10:g.110811242_110811249dup	NC_000001.10:g.110811241_110811249dup	NC_000001.10:g.110811240_110811249dup	NC_000001.10:g.110811239_110811249dup	NC_000001.10:g.110811238_110811249dup	NC_000001.10:g.110811249_110811250insAAAAAAAAAAAAAAAAAAA	NC_000001.10:g.110811249_110811250insAAAAAAAAAAAAAAAAAAAAA
KCNC4 transcript variant X1	XM_006710625.5:c.1820-13923=	XM_006710625.5:c.1820-13918_1820-13907del	XM_006710625.5:c.1820-13914_1820-13907del	XM_006710625.5:c.1820-13913_1820-13907del	XM_006710625.5:c.1820-13912_1820-13907del	XM_006710625.5:c.1820-13911_1820-13907del	XM_006710625.5:c.1820-13910_1820-13907del	XM_006710625.5:c.1820-13909_1820-13907del	XM_006710625.5:c.1820-13908_1820-13907del	XM_006710625.5:c.1820-13907del	XM_006710625.5:c.1820-13907dup	XM_006710625.5:c.1820-13908_1820-13907dup	XM_006710625.5:c.1820-13909_1820-13907dup	XM_006710625.5:c.1820-13910_1820-13907dup	XM_006710625.5:c.1820-13911_1820-13907dup	XM_006710625.5:c.1820-13912_1820-13907dup	XM_006710625.5:c.1820-13913_1820-13907dup	XM_006710625.5:c.1820-13914_1820-13907dup	XM_006710625.5:c.1820-13915_1820-13907dup	XM_006710625.5:c.1820-13916_1820-13907dup	XM_006710625.5:c.1820-13917_1820-13907dup	XM_006710625.5:c.1820-13918_1820-13907dup	XM_006710625.5:c.1820-13907_1820-13906insAAAAAAAAAAAAAAAAAAA	XM_006710625.5:c.1820-13907_1820-13906insAAAAAAAAAAAAAAAAAAAAA
KCNC4 transcript variant X3	XM_047419679.1:c.883-13923=	XM_047419679.1:c.883-13918_883-13907del	XM_047419679.1:c.883-13914_883-13907del	XM_047419679.1:c.883-13913_883-13907del	XM_047419679.1:c.883-13912_883-13907del	XM_047419679.1:c.883-13911_883-13907del	XM_047419679.1:c.883-13910_883-13907del	XM_047419679.1:c.883-13909_883-13907del	XM_047419679.1:c.883-13908_883-13907del	XM_047419679.1:c.883-13907del	XM_047419679.1:c.883-13907dup	XM_047419679.1:c.883-13908_883-13907dup	XM_047419679.1:c.883-13909_883-13907dup	XM_047419679.1:c.883-13910_883-13907dup	XM_047419679.1:c.883-13911_883-13907dup	XM_047419679.1:c.883-13912_883-13907dup	XM_047419679.1:c.883-13913_883-13907dup	XM_047419679.1:c.883-13914_883-13907dup	XM_047419679.1:c.883-13915_883-13907dup	XM_047419679.1:c.883-13916_883-13907dup	XM_047419679.1:c.883-13917_883-13907dup	XM_047419679.1:c.883-13918_883-13907dup	XM_047419679.1:c.883-13907_883-13906insAAAAAAAAAAAAAAAAAAA	XM_047419679.1:c.883-13907_883-13906insAAAAAAAAAAAAAAAAAAAAA

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#.

52 SubSNP, 37 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss2987427692	Nov 08, 2017 (151)
2	SWEGEN	ss2987427694	Nov 08, 2017 (151)
3	EVA_DECODE	ss3687516977	Jul 12, 2019 (153)
4	EVA_DECODE	ss3687516978	Jul 12, 2019 (153)
5	EVA_DECODE	ss3687516979	Jul 12, 2019 (153)
6	EVA_DECODE	ss3687516980	Jul 12, 2019 (153)
7	EVA_DECODE	ss3687516981	Jul 12, 2019 (153)
8	PACBIO	ss3783517420	Jul 12, 2019 (153)
9	PACBIO	ss3789159533	Jul 12, 2019 (153)
10	PACBIO	ss3794032445	Jul 12, 2019 (153)
11	KOGIC	ss3945233648	Apr 25, 2020 (154)
12	KOGIC	ss3945233649	Apr 25, 2020 (154)
13	KOGIC	ss3945233650	Apr 25, 2020 (154)
14	KOGIC	ss3945233651	Apr 25, 2020 (154)
15	GNOMAD	ss4000323576	Apr 25, 2021 (155)
16	GNOMAD	ss4000323577	Apr 25, 2021 (155)
17	GNOMAD	ss4000323578	Apr 25, 2021 (155)
18	GNOMAD	ss4000323579	Apr 25, 2021 (155)
19	GNOMAD	ss4000323580	Apr 25, 2021 (155)
20	GNOMAD	ss4000323581	Apr 25, 2021 (155)
21	GNOMAD	ss4000323582	Apr 25, 2021 (155)
22	GNOMAD	ss4000323583	Apr 25, 2021 (155)
23	GNOMAD	ss4000323584	Apr 25, 2021 (155)
24	GNOMAD	ss4000323585	Apr 25, 2021 (155)
25	GNOMAD	ss4000323586	Apr 25, 2021 (155)
26	GNOMAD	ss4000323587	Apr 25, 2021 (155)
27	GNOMAD	ss4000323588	Apr 25, 2021 (155)
28	GNOMAD	ss4000323589	Apr 25, 2021 (155)
29	GNOMAD	ss4000323590	Apr 25, 2021 (155)
30	GNOMAD	ss4000323591	Apr 25, 2021 (155)
31	GNOMAD	ss4000323592	Apr 25, 2021 (155)
32	GNOMAD	ss4000323593	Apr 25, 2021 (155)
33	GNOMAD	ss4000323594	Apr 25, 2021 (155)
34	GNOMAD	ss4000323595	Apr 25, 2021 (155)
35	GNOMAD	ss4000323596	Apr 25, 2021 (155)
36	GNOMAD	ss4000323597	Apr 25, 2021 (155)
37	TOPMED	ss4463367013	Apr 25, 2021 (155)
38	TOMMO_GENOMICS	ss5145651099	Apr 25, 2021 (155)
39	TOMMO_GENOMICS	ss5145651100	Apr 25, 2021 (155)
40	TOMMO_GENOMICS	ss5145651101	Apr 25, 2021 (155)
41	TOMMO_GENOMICS	ss5145651102	Apr 25, 2021 (155)
42	TOMMO_GENOMICS	ss5145651103	Apr 25, 2021 (155)
43	1000G_HIGH_COVERAGE	ss5243586408	Oct 12, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5243586409	Oct 12, 2022 (156)
45	HUGCELL_USP	ss5444512511	Oct 12, 2022 (156)
46	HUGCELL_USP	ss5444512512	Oct 12, 2022 (156)
47	HUGCELL_USP	ss5444512514	Oct 12, 2022 (156)
48	HUGCELL_USP	ss5444512515	Oct 12, 2022 (156)
49	TOMMO_GENOMICS	ss5670910187	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5670910188	Oct 12, 2022 (156)
51	TOMMO_GENOMICS	ss5670910190	Oct 12, 2022 (156)
52	TOMMO_GENOMICS	ss5670910191	Oct 12, 2022 (156)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22498339 (NC_000001.11:110268610::A 20955/76284) Row 22498340 (NC_000001.11:110268610::AA 8750/76114) Row 22498341 (NC_000001.11:110268610::AAA 40/76124)...	-	Apr 25, 2021 (155)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 1611649 (NC_000001.11:110268611::A 207/1572) Row 1611650 (NC_000001.11:110268611::AA 157/1572) Row 1611651 (NC_000001.11:110268610:A: 108/1572)...	-	Apr 25, 2020 (154)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 1611649 (NC_000001.11:110268611::A 207/1572) Row 1611650 (NC_000001.11:110268611::AA 157/1572) Row 1611651 (NC_000001.11:110268610:A: 108/1572)...	-	Apr 25, 2020 (154)
77	Korean Genome Project Submission ignored due to conflicting rows: Row 1611649 (NC_000001.11:110268611::A 207/1572) Row 1611650 (NC_000001.11:110268611::AA 157/1572) Row 1611651 (NC_000001.11:110268610:A: 108/1572)...	-	Apr 25, 2020 (154)
78	Korean Genome Project Submission ignored due to conflicting rows: Row 1611649 (NC_000001.11:110268611::A 207/1572) Row 1611650 (NC_000001.11:110268611::AA 157/1572) Row 1611651 (NC_000001.11:110268610:A: 108/1572)...	-	Apr 25, 2020 (154)
79	8.3KJPN Submission ignored due to conflicting rows: Row 3620406 (NC_000001.10:110811232::A 1494/15476) Row 3620407 (NC_000001.10:110811232:A: 553/15476) Row 3620408 (NC_000001.10:110811232::AA 1661/15476)...	-	Apr 25, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 3620406 (NC_000001.10:110811232::A 1494/15476) Row 3620407 (NC_000001.10:110811232:A: 553/15476) Row 3620408 (NC_000001.10:110811232::AA 1661/15476)...	-	Apr 25, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 3620406 (NC_000001.10:110811232::A 1494/15476) Row 3620407 (NC_000001.10:110811232:A: 553/15476) Row 3620408 (NC_000001.10:110811232::AA 1661/15476)...	-	Apr 25, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 3620406 (NC_000001.10:110811232::A 1494/15476) Row 3620407 (NC_000001.10:110811232:A: 553/15476) Row 3620408 (NC_000001.10:110811232::AA 1661/15476)...	-	Apr 25, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 3620406 (NC_000001.10:110811232::A 1494/15476) Row 3620407 (NC_000001.10:110811232:A: 553/15476) Row 3620408 (NC_000001.10:110811232::AA 1661/15476)...	-	Apr 25, 2021 (155)
84	14KJPN Submission ignored due to conflicting rows: Row 4747291 (NC_000001.11:110268610:A: 951/27744) Row 4747292 (NC_000001.11:110268610::AA 3116/27744) Row 4747294 (NC_000001.11:110268610::A 2768/27744)...	-	Oct 12, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 4747291 (NC_000001.11:110268610:A: 951/27744) Row 4747292 (NC_000001.11:110268610::AA 3116/27744) Row 4747294 (NC_000001.11:110268610::A 2768/27744)...	-	Oct 12, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 4747291 (NC_000001.11:110268610:A: 951/27744) Row 4747292 (NC_000001.11:110268610::AA 3116/27744) Row 4747294 (NC_000001.11:110268610::A 2768/27744)...	-	Oct 12, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 4747291 (NC_000001.11:110268610:A: 951/27744) Row 4747292 (NC_000001.11:110268610::AA 3116/27744) Row 4747294 (NC_000001.11:110268610::A 2768/27744)...	-	Oct 12, 2022 (156)
88	TopMed	NC_000001.11 - 110268611	Apr 25, 2021 (155)
89	ALFA	NC_000001.11 - 110268611	Apr 25, 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
ss4000323597	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAA:	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
26973348, ss4000323596, ss4463367013	NC_000001.11:110268610:AAAAAAA:	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4000323595	NC_000001.11:110268610:AAAAAA:	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4000323594	NC_000001.11:110268610:AAAAA:	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4000323593	NC_000001.11:110268610:AAAA:	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4000323592	NC_000001.11:110268610:AAA:	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3687516981, ss4000323591	NC_000001.11:110268610:AA:	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5145651100	NC_000001.10:110811232:A:	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3945233650, ss4000323590, ss5243586408, ss5444512514, ss5670910187	NC_000001.11:110268610:A:	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3687516980	NC_000001.11:110268611:A:	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss2987427692, ss3783517420, ss3789159533, ss3794032445, ss5145651099	NC_000001.10:110811232::A	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4000323576, ss5444512511, ss5670910190	NC_000001.11:110268610::A	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3945233648	NC_000001.11:110268611::A	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3687516979	NC_000001.11:110268612::A	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss2987427694, ss5145651101	NC_000001.10:110811232::AA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4000323577, ss5243586409, ss5444512512, ss5670910188	NC_000001.11:110268610::AA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3945233649	NC_000001.11:110268611::AA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3687516978	NC_000001.11:110268612::AA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4000323578, ss5444512515	NC_000001.11:110268610::AAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3945233651	NC_000001.11:110268611::AAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4000323579	NC_000001.11:110268610::AAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3687516977	NC_000001.11:110268612::AAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5145651103	NC_000001.10:110811232::AAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4000323580	NC_000001.11:110268610::AAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
8700629395	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4000323581	NC_000001.11:110268610::AAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5145651102	NC_000001.10:110811232::AAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4000323582, ss5670910191	NC_000001.11:110268610::AAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4000323583	NC_000001.11:110268610::AAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4000323584	NC_000001.11:110268610::AAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4000323585	NC_000001.11:110268610::AAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4000323586	NC_000001.11:110268610::AAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4000323587	NC_000001.11:110268610::AAAAAAAAAA… NC_000001.11:110268610::AAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4000323588	NC_000001.11:110268610::AAAAAAAAAA… NC_000001.11:110268610::AAAAAAAAAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4000323589	NC_000001.11:110268610::AAAAAAAAAA… NC_000001.11:110268610::AAAAAAAAAAAAAAAAAAAAA	NC_000001.11:110268610:AAAAAAAAAAA… NC_000001.11:110268610:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs1177241176

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

rs1177241176