Name: rs1553754813
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.

rs1553754813

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:118933471-118933490 (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: delTATA / delTA / dupTA / dupTATA …
delTATA / delTA / dupTA / dupTATA / dup(TA)₃ / dup(TA)₄ / dup(TA)₅ / dup(TA)₆ / dup(TA)₇ / dup(TA)₈ / dup(TA)₉ / dup(TA)₁₀ / ins(TA)₁₁ / ins(TA)₁₂
Variation Type: Indel Insertion and Deletion
Frequency: dup(TA)₆=0.00985 (128/12995, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IGSF11 : 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	HTRZ	HWEP
Total	Global	12995	TATATATATATATATATATA=0.98192	TATATATATATATATA=0.00000, TATATATATATATATATA=0.00000, TATATATATATATATATATATA=0.00077, TATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATATATATA=0.00985, TATATATATATATATATATATATATATATATATATA=0.00085, TATATATATATATATATATATATATATATATATA=0.00662, TATATATATATATATATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATATATATATATATATATA=0.00000	0.986109	0.013891	0
European	Sub	10107	TATATATATATATATATATA=0.97675	TATATATATATATATA=0.00000, TATATATATATATATATA=0.00000, TATATATATATATATATATATA=0.00099, TATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATATATATA=0.01266, TATATATATATATATATATATATATATATATATATA=0.00109, TATATATATATATATATATATATATATATATATA=0.00851, TATATATATATATATATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATATATATATATATATA=0.00000, TATATATATATATATATATATATATATATATATATATATATA=0.00000	0.981686	0.018314	0
African	Sub	1844	TATATATATATATATATATA=1.0000	TATATATATATATATA=0.0000, TATATATATATATATATA=0.0000, TATATATATATATATATATATA=0.0000, TATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATATATATATATA=0.0000	1.0	0.0	N/A
African Others	Sub	74	TATATATATATATATATATA=1.00	TATATATATATATATA=0.00, TATATATATATATATATA=0.00, TATATATATATATATATATATA=0.00, TATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATATATA=0.00	1.0	0.0	N/A
African American	Sub	1770	TATATATATATATATATATA=1.0000	TATATATATATATATA=0.0000, TATATATATATATATATA=0.0000, TATATATATATATATATATATA=0.0000, TATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATATATATATA=0.0000, TATATATATATATATATATATATATATATATATATATATATA=0.0000	1.0	0.0	N/A
Asian	Sub	90	TATATATATATATATATATA=1.00	TATATATATATATATA=0.00, TATATATATATATATATA=0.00, TATATATATATATATATATATA=0.00, TATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATATATA=0.00	1.0	0.0	N/A
East Asian	Sub	70	TATATATATATATATATATA=1.00	TATATATATATATATA=0.00, TATATATATATATATATA=0.00, TATATATATATATATATATATA=0.00, TATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATATATA=0.00	1.0	0.0	N/A
Other Asian	Sub	20	TATATATATATATATATATA=1.00	TATATATATATATATA=0.00, TATATATATATATATATA=0.00, TATATATATATATATATATATA=0.00, TATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATATATA=0.00	1.0	0.0	N/A
Latin American 1	Sub	118	TATATATATATATATATATA=1.000	TATATATATATATATA=0.000, TATATATATATATATATA=0.000, TATATATATATATATATATATA=0.000, TATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATATATATA=0.000	1.0	0.0	N/A
Latin American 2	Sub	368	TATATATATATATATATATA=1.000	TATATATATATATATA=0.000, TATATATATATATATATA=0.000, TATATATATATATATATATATA=0.000, TATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATATATATA=0.000	1.0	0.0	N/A
South Asian	Sub	86	TATATATATATATATATATA=1.00	TATATATATATATATA=0.00, TATATATATATATATATA=0.00, TATATATATATATATATATATA=0.00, TATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATATA=0.00, TATATATATATATATATATATATATATATATATATATATATA=0.00	1.0	0.0	N/A
Other	Sub	382	TATATATATATATATATATA=1.000	TATATATATATATATA=0.000, TATATATATATATATATA=0.000, TATATATATATATATATATATA=0.000, TATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATATATA=0.000, TATATATATATATATATATATATATATATATATATATATATA=0.000	1.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	12995	(TA)₁₀=0.98192	delTATA=0.00000, delTA=0.00000, dupTA=0.00077, dupTATA=0.00000, dup(TA)₃=0.00000, dup(TA)₄=0.00000, dup(TA)₅=0.00000, dup(TA)₆=0.00985, dup(TA)₇=0.00662, dup(TA)₈=0.00085, dup(TA)₉=0.00000, dup(TA)₁₀=0.00000, ins(TA)₁₁=0.00000
Allele Frequency Aggregator	European	Sub	10107	(TA)₁₀=0.97675	delTATA=0.00000, delTA=0.00000, dupTA=0.00099, dupTATA=0.00000, dup(TA)₃=0.00000, dup(TA)₄=0.00000, dup(TA)₅=0.00000, dup(TA)₆=0.01266, dup(TA)₇=0.00851, dup(TA)₈=0.00109, dup(TA)₉=0.00000, dup(TA)₁₀=0.00000, ins(TA)₁₁=0.00000
Allele Frequency Aggregator	African	Sub	1844	(TA)₁₀=1.0000	delTATA=0.0000, delTA=0.0000, dupTA=0.0000, dupTATA=0.0000, dup(TA)₃=0.0000, dup(TA)₄=0.0000, dup(TA)₅=0.0000, dup(TA)₆=0.0000, dup(TA)₇=0.0000, dup(TA)₈=0.0000, dup(TA)₉=0.0000, dup(TA)₁₀=0.0000, ins(TA)₁₁=0.0000
Allele Frequency Aggregator	Other	Sub	382	(TA)₁₀=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000, dup(TA)₆=0.000, dup(TA)₇=0.000, dup(TA)₈=0.000, dup(TA)₉=0.000, dup(TA)₁₀=0.000, ins(TA)₁₁=0.000
Allele Frequency Aggregator	Latin American 2	Sub	368	(TA)₁₀=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000, dup(TA)₆=0.000, dup(TA)₇=0.000, dup(TA)₈=0.000, dup(TA)₉=0.000, dup(TA)₁₀=0.000, ins(TA)₁₁=0.000
Allele Frequency Aggregator	Latin American 1	Sub	118	(TA)₁₀=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000, dup(TA)₆=0.000, dup(TA)₇=0.000, dup(TA)₈=0.000, dup(TA)₉=0.000, dup(TA)₁₀=0.000, ins(TA)₁₁=0.000
Allele Frequency Aggregator	Asian	Sub	90	(TA)₁₀=1.00	delTATA=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00, dup(TA)₆=0.00, dup(TA)₇=0.00, dup(TA)₈=0.00, dup(TA)₉=0.00, dup(TA)₁₀=0.00, ins(TA)₁₁=0.00
Allele Frequency Aggregator	South Asian	Sub	86	(TA)₁₀=1.00	delTATA=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00, dup(TA)₆=0.00, dup(TA)₇=0.00, dup(TA)₈=0.00, dup(TA)₉=0.00, dup(TA)₁₀=0.00, ins(TA)₁₁=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 3	NC_000003.12:g.118933471TA[8]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[9]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[11]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[12]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[13]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[14]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[15]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[16]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[17]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[18]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[19]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[20]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[21]
GRCh38.p14 chr 3	NC_000003.12:g.118933471TA[22]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[8]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[9]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[11]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[12]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[13]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[14]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[15]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[16]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[17]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[18]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[19]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[20]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[21]
GRCh37.p13 chr 3	NC_000003.11:g.118652318TA[22]

Gene: IGSF11, immunoglobulin superfamily member 11 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IGSF11 transcript variant 2	NM_001015887.3:c.53-3215T… NM_001015887.3:c.53-3215TA[8]	N/A	Intron Variant
IGSF11 transcript variant 3	NM_001353318.2:c.203-3215… NM_001353318.2:c.203-3215TA[8]	N/A	Intron Variant
IGSF11 transcript variant 4	NM_001353319.2:c.203-3215… NM_001353319.2:c.203-3215TA[8]	N/A	Intron Variant
IGSF11 transcript variant 5	NM_001353320.2:c.50-3215T… NM_001353320.2:c.50-3215TA[8]	N/A	Intron Variant
IGSF11 transcript variant 6	NM_001353321.2:c.53-3215T… NM_001353321.2:c.53-3215TA[8]	N/A	Intron Variant
IGSF11 transcript variant 7	NM_001353322.2:c.50-3215T… NM_001353322.2:c.50-3215TA[8]	N/A	Intron Variant
IGSF11 transcript variant 8	NM_001353323.2:c.53-3215T… NM_001353323.2:c.53-3215TA[8]	N/A	Intron Variant
IGSF11 transcript variant 9	NM_001353324.2:c.53-3215T… NM_001353324.2:c.53-3215TA[8]	N/A	Intron Variant
IGSF11 transcript variant 10	NM_001353325.2:c.-125-321… NM_001353325.2:c.-125-3215TA[8]	N/A	Intron Variant
IGSF11 transcript variant 11	NM_001353326.2:c.-125-321… NM_001353326.2:c.-125-3215TA[8]	N/A	Intron Variant
IGSF11 transcript variant 1	NM_152538.4:c.50-3215TA[8]	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	(TA)₁₀=	delTATA	delTA	dupTA	dupTATA	dup(TA)₃	dup(TA)₄	dup(TA)₅	dup(TA)₆	dup(TA)₇	dup(TA)₈	dup(TA)₉	dup(TA)₁₀	ins(TA)₁₁	ins(TA)₁₂
GRCh38.p14 chr 3	NC_000003.12:g.118933471_118933490=	NC_000003.12:g.118933471TA[8]	NC_000003.12:g.118933471TA[9]	NC_000003.12:g.118933471TA[11]	NC_000003.12:g.118933471TA[12]	NC_000003.12:g.118933471TA[13]	NC_000003.12:g.118933471TA[14]	NC_000003.12:g.118933471TA[15]	NC_000003.12:g.118933471TA[16]	NC_000003.12:g.118933471TA[17]	NC_000003.12:g.118933471TA[18]	NC_000003.12:g.118933471TA[19]	NC_000003.12:g.118933471TA[20]	NC_000003.12:g.118933471TA[21]	NC_000003.12:g.118933471TA[22]
GRCh37.p13 chr 3	NC_000003.11:g.118652318_118652337=	NC_000003.11:g.118652318TA[8]	NC_000003.11:g.118652318TA[9]	NC_000003.11:g.118652318TA[11]	NC_000003.11:g.118652318TA[12]	NC_000003.11:g.118652318TA[13]	NC_000003.11:g.118652318TA[14]	NC_000003.11:g.118652318TA[15]	NC_000003.11:g.118652318TA[16]	NC_000003.11:g.118652318TA[17]	NC_000003.11:g.118652318TA[18]	NC_000003.11:g.118652318TA[19]	NC_000003.11:g.118652318TA[20]	NC_000003.11:g.118652318TA[21]	NC_000003.11:g.118652318TA[22]
IGSF11 transcript variant 2	NM_001015887.1:c.53-3196=	NM_001015887.1:c.53-3215TA[8]	NM_001015887.1:c.53-3215TA[9]	NM_001015887.1:c.53-3215TA[11]	NM_001015887.1:c.53-3215TA[12]	NM_001015887.1:c.53-3215TA[13]	NM_001015887.1:c.53-3215TA[14]	NM_001015887.1:c.53-3215TA[15]	NM_001015887.1:c.53-3215TA[16]	NM_001015887.1:c.53-3215TA[17]	NM_001015887.1:c.53-3215TA[18]	NM_001015887.1:c.53-3215TA[19]	NM_001015887.1:c.53-3215TA[20]	NM_001015887.1:c.53-3215TA[21]	NM_001015887.1:c.53-3215TA[22]
IGSF11 transcript variant 2	NM_001015887.3:c.53-3196=	NM_001015887.3:c.53-3215TA[8]	NM_001015887.3:c.53-3215TA[9]	NM_001015887.3:c.53-3215TA[11]	NM_001015887.3:c.53-3215TA[12]	NM_001015887.3:c.53-3215TA[13]	NM_001015887.3:c.53-3215TA[14]	NM_001015887.3:c.53-3215TA[15]	NM_001015887.3:c.53-3215TA[16]	NM_001015887.3:c.53-3215TA[17]	NM_001015887.3:c.53-3215TA[18]	NM_001015887.3:c.53-3215TA[19]	NM_001015887.3:c.53-3215TA[20]	NM_001015887.3:c.53-3215TA[21]	NM_001015887.3:c.53-3215TA[22]
IGSF11 transcript variant 3	NM_001353318.2:c.203-3196=	NM_001353318.2:c.203-3215TA[8]	NM_001353318.2:c.203-3215TA[9]	NM_001353318.2:c.203-3215TA[11]	NM_001353318.2:c.203-3215TA[12]	NM_001353318.2:c.203-3215TA[13]	NM_001353318.2:c.203-3215TA[14]	NM_001353318.2:c.203-3215TA[15]	NM_001353318.2:c.203-3215TA[16]	NM_001353318.2:c.203-3215TA[17]	NM_001353318.2:c.203-3215TA[18]	NM_001353318.2:c.203-3215TA[19]	NM_001353318.2:c.203-3215TA[20]	NM_001353318.2:c.203-3215TA[21]	NM_001353318.2:c.203-3215TA[22]
IGSF11 transcript variant 4	NM_001353319.2:c.203-3196=	NM_001353319.2:c.203-3215TA[8]	NM_001353319.2:c.203-3215TA[9]	NM_001353319.2:c.203-3215TA[11]	NM_001353319.2:c.203-3215TA[12]	NM_001353319.2:c.203-3215TA[13]	NM_001353319.2:c.203-3215TA[14]	NM_001353319.2:c.203-3215TA[15]	NM_001353319.2:c.203-3215TA[16]	NM_001353319.2:c.203-3215TA[17]	NM_001353319.2:c.203-3215TA[18]	NM_001353319.2:c.203-3215TA[19]	NM_001353319.2:c.203-3215TA[20]	NM_001353319.2:c.203-3215TA[21]	NM_001353319.2:c.203-3215TA[22]
IGSF11 transcript variant 5	NM_001353320.2:c.50-3196=	NM_001353320.2:c.50-3215TA[8]	NM_001353320.2:c.50-3215TA[9]	NM_001353320.2:c.50-3215TA[11]	NM_001353320.2:c.50-3215TA[12]	NM_001353320.2:c.50-3215TA[13]	NM_001353320.2:c.50-3215TA[14]	NM_001353320.2:c.50-3215TA[15]	NM_001353320.2:c.50-3215TA[16]	NM_001353320.2:c.50-3215TA[17]	NM_001353320.2:c.50-3215TA[18]	NM_001353320.2:c.50-3215TA[19]	NM_001353320.2:c.50-3215TA[20]	NM_001353320.2:c.50-3215TA[21]	NM_001353320.2:c.50-3215TA[22]
IGSF11 transcript variant 6	NM_001353321.2:c.53-3196=	NM_001353321.2:c.53-3215TA[8]	NM_001353321.2:c.53-3215TA[9]	NM_001353321.2:c.53-3215TA[11]	NM_001353321.2:c.53-3215TA[12]	NM_001353321.2:c.53-3215TA[13]	NM_001353321.2:c.53-3215TA[14]	NM_001353321.2:c.53-3215TA[15]	NM_001353321.2:c.53-3215TA[16]	NM_001353321.2:c.53-3215TA[17]	NM_001353321.2:c.53-3215TA[18]	NM_001353321.2:c.53-3215TA[19]	NM_001353321.2:c.53-3215TA[20]	NM_001353321.2:c.53-3215TA[21]	NM_001353321.2:c.53-3215TA[22]
IGSF11 transcript variant 7	NM_001353322.2:c.50-3196=	NM_001353322.2:c.50-3215TA[8]	NM_001353322.2:c.50-3215TA[9]	NM_001353322.2:c.50-3215TA[11]	NM_001353322.2:c.50-3215TA[12]	NM_001353322.2:c.50-3215TA[13]	NM_001353322.2:c.50-3215TA[14]	NM_001353322.2:c.50-3215TA[15]	NM_001353322.2:c.50-3215TA[16]	NM_001353322.2:c.50-3215TA[17]	NM_001353322.2:c.50-3215TA[18]	NM_001353322.2:c.50-3215TA[19]	NM_001353322.2:c.50-3215TA[20]	NM_001353322.2:c.50-3215TA[21]	NM_001353322.2:c.50-3215TA[22]
IGSF11 transcript variant 8	NM_001353323.2:c.53-3196=	NM_001353323.2:c.53-3215TA[8]	NM_001353323.2:c.53-3215TA[9]	NM_001353323.2:c.53-3215TA[11]	NM_001353323.2:c.53-3215TA[12]	NM_001353323.2:c.53-3215TA[13]	NM_001353323.2:c.53-3215TA[14]	NM_001353323.2:c.53-3215TA[15]	NM_001353323.2:c.53-3215TA[16]	NM_001353323.2:c.53-3215TA[17]	NM_001353323.2:c.53-3215TA[18]	NM_001353323.2:c.53-3215TA[19]	NM_001353323.2:c.53-3215TA[20]	NM_001353323.2:c.53-3215TA[21]	NM_001353323.2:c.53-3215TA[22]
IGSF11 transcript variant 9	NM_001353324.2:c.53-3196=	NM_001353324.2:c.53-3215TA[8]	NM_001353324.2:c.53-3215TA[9]	NM_001353324.2:c.53-3215TA[11]	NM_001353324.2:c.53-3215TA[12]	NM_001353324.2:c.53-3215TA[13]	NM_001353324.2:c.53-3215TA[14]	NM_001353324.2:c.53-3215TA[15]	NM_001353324.2:c.53-3215TA[16]	NM_001353324.2:c.53-3215TA[17]	NM_001353324.2:c.53-3215TA[18]	NM_001353324.2:c.53-3215TA[19]	NM_001353324.2:c.53-3215TA[20]	NM_001353324.2:c.53-3215TA[21]	NM_001353324.2:c.53-3215TA[22]
IGSF11 transcript variant 10	NM_001353325.2:c.-125-3196=	NM_001353325.2:c.-125-3215TA[8]	NM_001353325.2:c.-125-3215TA[9]	NM_001353325.2:c.-125-3215TA[11]	NM_001353325.2:c.-125-3215TA[12]	NM_001353325.2:c.-125-3215TA[13]	NM_001353325.2:c.-125-3215TA[14]	NM_001353325.2:c.-125-3215TA[15]	NM_001353325.2:c.-125-3215TA[16]	NM_001353325.2:c.-125-3215TA[17]	NM_001353325.2:c.-125-3215TA[18]	NM_001353325.2:c.-125-3215TA[19]	NM_001353325.2:c.-125-3215TA[20]	NM_001353325.2:c.-125-3215TA[21]	NM_001353325.2:c.-125-3215TA[22]
IGSF11 transcript variant 11	NM_001353326.2:c.-125-3196=	NM_001353326.2:c.-125-3215TA[8]	NM_001353326.2:c.-125-3215TA[9]	NM_001353326.2:c.-125-3215TA[11]	NM_001353326.2:c.-125-3215TA[12]	NM_001353326.2:c.-125-3215TA[13]	NM_001353326.2:c.-125-3215TA[14]	NM_001353326.2:c.-125-3215TA[15]	NM_001353326.2:c.-125-3215TA[16]	NM_001353326.2:c.-125-3215TA[17]	NM_001353326.2:c.-125-3215TA[18]	NM_001353326.2:c.-125-3215TA[19]	NM_001353326.2:c.-125-3215TA[20]	NM_001353326.2:c.-125-3215TA[21]	NM_001353326.2:c.-125-3215TA[22]
IGSF11 transcript variant 1	NM_152538.2:c.50-3196=	NM_152538.2:c.50-3215TA[8]	NM_152538.2:c.50-3215TA[9]	NM_152538.2:c.50-3215TA[11]	NM_152538.2:c.50-3215TA[12]	NM_152538.2:c.50-3215TA[13]	NM_152538.2:c.50-3215TA[14]	NM_152538.2:c.50-3215TA[15]	NM_152538.2:c.50-3215TA[16]	NM_152538.2:c.50-3215TA[17]	NM_152538.2:c.50-3215TA[18]	NM_152538.2:c.50-3215TA[19]	NM_152538.2:c.50-3215TA[20]	NM_152538.2:c.50-3215TA[21]	NM_152538.2:c.50-3215TA[22]
IGSF11 transcript variant 1	NM_152538.4:c.50-3196=	NM_152538.4:c.50-3215TA[8]	NM_152538.4:c.50-3215TA[9]	NM_152538.4:c.50-3215TA[11]	NM_152538.4:c.50-3215TA[12]	NM_152538.4:c.50-3215TA[13]	NM_152538.4:c.50-3215TA[14]	NM_152538.4:c.50-3215TA[15]	NM_152538.4:c.50-3215TA[16]	NM_152538.4:c.50-3215TA[17]	NM_152538.4:c.50-3215TA[18]	NM_152538.4:c.50-3215TA[19]	NM_152538.4:c.50-3215TA[20]	NM_152538.4:c.50-3215TA[21]	NM_152538.4:c.50-3215TA[22]
IGSF11 transcript variant X1	XM_005247144.1:c.50-3196=	XM_005247144.1:c.50-3215TA[8]	XM_005247144.1:c.50-3215TA[9]	XM_005247144.1:c.50-3215TA[11]	XM_005247144.1:c.50-3215TA[12]	XM_005247144.1:c.50-3215TA[13]	XM_005247144.1:c.50-3215TA[14]	XM_005247144.1:c.50-3215TA[15]	XM_005247144.1:c.50-3215TA[16]	XM_005247144.1:c.50-3215TA[17]	XM_005247144.1:c.50-3215TA[18]	XM_005247144.1:c.50-3215TA[19]	XM_005247144.1:c.50-3215TA[20]	XM_005247144.1:c.50-3215TA[21]	XM_005247144.1:c.50-3215TA[22]
IGSF11 transcript variant X2	XM_005247145.1:c.50-3196=	XM_005247145.1:c.50-3215TA[8]	XM_005247145.1:c.50-3215TA[9]	XM_005247145.1:c.50-3215TA[11]	XM_005247145.1:c.50-3215TA[12]	XM_005247145.1:c.50-3215TA[13]	XM_005247145.1:c.50-3215TA[14]	XM_005247145.1:c.50-3215TA[15]	XM_005247145.1:c.50-3215TA[16]	XM_005247145.1:c.50-3215TA[17]	XM_005247145.1:c.50-3215TA[18]	XM_005247145.1:c.50-3215TA[19]	XM_005247145.1:c.50-3215TA[20]	XM_005247145.1:c.50-3215TA[21]	XM_005247145.1:c.50-3215TA[22]
IGSF11 transcript variant X3	XM_005247146.1:c.53-3196=	XM_005247146.1:c.53-3215TA[8]	XM_005247146.1:c.53-3215TA[9]	XM_005247146.1:c.53-3215TA[11]	XM_005247146.1:c.53-3215TA[12]	XM_005247146.1:c.53-3215TA[13]	XM_005247146.1:c.53-3215TA[14]	XM_005247146.1:c.53-3215TA[15]	XM_005247146.1:c.53-3215TA[16]	XM_005247146.1:c.53-3215TA[17]	XM_005247146.1:c.53-3215TA[18]	XM_005247146.1:c.53-3215TA[19]	XM_005247146.1:c.53-3215TA[20]	XM_005247146.1:c.53-3215TA[21]	XM_005247146.1:c.53-3215TA[22]
IGSF11 transcript variant X4	XM_005247147.1:c.50-3196=	XM_005247147.1:c.50-3215TA[8]	XM_005247147.1:c.50-3215TA[9]	XM_005247147.1:c.50-3215TA[11]	XM_005247147.1:c.50-3215TA[12]	XM_005247147.1:c.50-3215TA[13]	XM_005247147.1:c.50-3215TA[14]	XM_005247147.1:c.50-3215TA[15]	XM_005247147.1:c.50-3215TA[16]	XM_005247147.1:c.50-3215TA[17]	XM_005247147.1:c.50-3215TA[18]	XM_005247147.1:c.50-3215TA[19]	XM_005247147.1:c.50-3215TA[20]	XM_005247147.1:c.50-3215TA[21]	XM_005247147.1:c.50-3215TA[22]
IGSF11 transcript variant X5	XM_005247148.1:c.53-3196=	XM_005247148.1:c.53-3215TA[8]	XM_005247148.1:c.53-3215TA[9]	XM_005247148.1:c.53-3215TA[11]	XM_005247148.1:c.53-3215TA[12]	XM_005247148.1:c.53-3215TA[13]	XM_005247148.1:c.53-3215TA[14]	XM_005247148.1:c.53-3215TA[15]	XM_005247148.1:c.53-3215TA[16]	XM_005247148.1:c.53-3215TA[17]	XM_005247148.1:c.53-3215TA[18]	XM_005247148.1:c.53-3215TA[19]	XM_005247148.1:c.53-3215TA[20]	XM_005247148.1:c.53-3215TA[21]	XM_005247148.1:c.53-3215TA[22]

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#.

31 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss2993055391	Nov 08, 2017 (151)
2	SWEGEN	ss2993055392	Nov 08, 2017 (151)
3	SWEGEN	ss2993055393	Nov 08, 2017 (151)
4	ACPOP	ss3730276359	Jul 13, 2019 (153)
5	ACPOP	ss3730276361	Jul 13, 2019 (153)
6	EVA	ss3828032051	Apr 25, 2020 (154)
7	GNOMAD	ss4079334552	Apr 26, 2021 (155)
8	GNOMAD	ss4079334553	Apr 26, 2021 (155)
9	GNOMAD	ss4079334554	Apr 26, 2021 (155)
10	GNOMAD	ss4079334555	Apr 26, 2021 (155)
11	GNOMAD	ss4079334556	Apr 26, 2021 (155)
12	GNOMAD	ss4079334557	Apr 26, 2021 (155)
13	GNOMAD	ss4079334558	Apr 26, 2021 (155)
14	GNOMAD	ss4079334559	Apr 26, 2021 (155)
15	GNOMAD	ss4079334560	Apr 26, 2021 (155)
16	GNOMAD	ss4079334561	Apr 26, 2021 (155)
17	GNOMAD	ss4079334562	Apr 26, 2021 (155)
18	GNOMAD	ss4079334563	Apr 26, 2021 (155)
19	GNOMAD	ss4079334570	Apr 26, 2021 (155)
20	GNOMAD	ss4079334571	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5161194045	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5161194046	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5161194048	Apr 26, 2021 (155)
24	1000G_HIGH_COVERAGE	ss5255729865	Oct 12, 2022 (156)
25	HUGCELL_USP	ss5454908272	Oct 12, 2022 (156)
26	HUGCELL_USP	ss5454908273	Oct 12, 2022 (156)
27	HUGCELL_USP	ss5454908276	Oct 12, 2022 (156)
28	TOMMO_GENOMICS	ss5693953904	Oct 12, 2022 (156)
29	TOMMO_GENOMICS	ss5693953906	Oct 12, 2022 (156)
30	TOMMO_GENOMICS	ss5693953908	Oct 12, 2022 (156)
31	EVA	ss5826366121	Oct 12, 2022 (156)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121330582 (NC_000003.12:118933470::TA 796/134364) Row 121330583 (NC_000003.12:118933470::TATA 3201/134394) Row 121330584 (NC_000003.12:118933470::TATATA 3569/134374)...	-	Apr 26, 2021 (155)
46	Northern Sweden Submission ignored due to conflicting rows: Row 3561224 (NC_000003.11:118652317::TA 1/600) Row 3561226 (NC_000003.11:118652317::TATATATATATA 16/600)	-	Jul 13, 2019 (153)
47	Northern Sweden Submission ignored due to conflicting rows: Row 3561224 (NC_000003.11:118652317::TA 1/600) Row 3561226 (NC_000003.11:118652317::TATATATATATA 16/600)	-	Jul 13, 2019 (153)
48	8.3KJPN Submission ignored due to conflicting rows: Row 19163352 (NC_000003.11:118652317::TATATATATATATA 133/16760) Row 19163353 (NC_000003.11:118652317::TA 489/16760) Row 19163355 (NC_000003.11:118652317::TATATATATATA 690/16760)	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 19163352 (NC_000003.11:118652317::TATATATATATATA 133/16760) Row 19163353 (NC_000003.11:118652317::TA 489/16760) Row 19163355 (NC_000003.11:118652317::TATATATATATA 690/16760)	-	Apr 26, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 19163352 (NC_000003.11:118652317::TATATATATATATA 133/16760) Row 19163353 (NC_000003.11:118652317::TA 489/16760) Row 19163355 (NC_000003.11:118652317::TATATATATATA 690/16760)	-	Apr 26, 2021 (155)
51	14KJPN Submission ignored due to conflicting rows: Row 27791008 (NC_000003.12:118933470::TA 829/28258) Row 27791010 (NC_000003.12:118933470::TATATATATATA 1143/28258) Row 27791012 (NC_000003.12:118933470::TATATATATATATA 203/28258)	-	Oct 12, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 27791008 (NC_000003.12:118933470::TA 829/28258) Row 27791010 (NC_000003.12:118933470::TATATATATATA 1143/28258) Row 27791012 (NC_000003.12:118933470::TATATATATATATA 203/28258)	-	Oct 12, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 27791008 (NC_000003.12:118933470::TA 829/28258) Row 27791010 (NC_000003.12:118933470::TATATATATATA 1143/28258) Row 27791012 (NC_000003.12:118933470::TATATATATATATA 203/28258)	-	Oct 12, 2022 (156)
54	ALFA	NC_000003.12 - 118933471	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).

Associated ID	History Updated (Build)
rs147548072	Oct 14, 2011 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4079334571	NC_000003.12:118933470:TATA:	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATA	(self)
ss3828032051, ss5826366121	NC_000003.11:118652317:TA:	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATA	(self)
ss4079334570	NC_000003.12:118933470:TA:	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATA	(self)
ss2993055391, ss3730276359, ss5161194046	NC_000003.11:118652317::TA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATA	(self)
ss4079334552, ss5693953904	NC_000003.12:118933470::TA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATA	(self)
ss4079334553, ss5454908276	NC_000003.12:118933470::TATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATA	(self)
ss4079334554, ss5255729865, ss5454908272	NC_000003.12:118933470::TATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATA	(self)
ss4079334555	NC_000003.12:118933470::TATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATA	(self)
ss4079334556	NC_000003.12:118933470::TATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATA	(self)
ss2993055392, ss3730276361, ss5161194048	NC_000003.11:118652317::TATATATATA… NC_000003.11:118652317::TATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATA	(self)
ss4079334557, ss5454908273, ss5693953906	NC_000003.12:118933470::TATATATATA… NC_000003.12:118933470::TATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATA	(self)
ss2993055393, ss5161194045	NC_000003.11:118652317::TATATATATA… NC_000003.11:118652317::TATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATA	(self)
ss4079334558, ss5693953908	NC_000003.12:118933470::TATATATATA… NC_000003.12:118933470::TATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATA	(self)
ss4079334559	NC_000003.12:118933470::TATATATATA… NC_000003.12:118933470::TATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATA	(self)
ss4079334560	NC_000003.12:118933470::TATATATATA… NC_000003.12:118933470::TATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATA	(self)
ss4079334561	NC_000003.12:118933470::TATATATATA… NC_000003.12:118933470::TATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATA	(self)
ss4079334562	NC_000003.12:118933470::TATATATATA… NC_000003.12:118933470::TATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATA	(self)
8379795980	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATA	(self)
ss4079334563	NC_000003.12:118933470::TATATATATA… NC_000003.12:118933470::TATATATATATATATATATATATA	NC_000003.12:118933470:TATATATATAT… NC_000003.12:118933470:TATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATA	(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 rs1553754813

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1553754813