Name: rs35180980
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.

rs35180980

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:111074628-111074648 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₂ / del(T)₉ / del(T)₇ / del…
del(T)₁₂ / del(T)₉ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / ins(T)₂₆
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1305 (916/7018, ALFA)
dupT=0.0809 (405/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TSLP : 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	7018	TTTTTTTTTTTTTTTTTTTTT=0.7867	TTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0711, TTTTTTTTTTTTTTTTTTTTTT=0.1305, TTTTTTTTTTTTTTTTTTTTTTTT=0.0081, TTTTTTTTTTTTTTTTTTTTTTT=0.0019, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0007, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0010	0.824198	0.073195	0.102607	32
European	Sub	6440	TTTTTTTTTTTTTTTTTTTTT=0.7682	TTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0772, TTTTTTTTTTTTTTTTTTTTTT=0.1419, TTTTTTTTTTTTTTTTTTTTTTTT=0.0089, TTTTTTTTTTTTTTTTTTTTTTT=0.0020, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0008, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0011	0.805915	0.080961	0.113124	32
African	Sub	322	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	12	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	310	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	26	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	24	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	28	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	94	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	100	TTTTTTTTTTTTTTTTTTTTT=0.96	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.979167	0.0	0.020833	0

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
Allele Frequency Aggregator	Total	Global	7018	(T)₂₁=0.7867	del(T)₁₂=0.0000, del(T)₉=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0711, dupT=0.1305, dupTT=0.0019, dupTTT=0.0081, dup(T)₄=0.0010, dup(T)₆=0.0007
Allele Frequency Aggregator	European	Sub	6440	(T)₂₁=0.7682	del(T)₁₂=0.0000, del(T)₉=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0772, dupT=0.1419, dupTT=0.0020, dupTTT=0.0089, dup(T)₄=0.0011, dup(T)₆=0.0008
Allele Frequency Aggregator	African	Sub	322	(T)₂₁=1.000	del(T)₁₂=0.000, del(T)₉=0.000, del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	100	(T)₂₁=0.96	del(T)₁₂=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.02, dupT=0.02, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Latin American 2	Sub	94	(T)₂₁=1.00	del(T)₁₂=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	28	(T)₂₁=1.00	del(T)₁₂=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Asian	Sub	26	(T)₂₁=1.00	del(T)₁₂=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	8	(T)₂₁=1.0	del(T)₁₂=0.0, del(T)₉=0.0, del(T)₇=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₆=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.0809
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.1762
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.0288
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.0567
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.053
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.049

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 5	NC_000005.10:g.111074637_111074648del
GRCh38.p14 chr 5	NC_000005.10:g.111074640_111074648del
GRCh38.p14 chr 5	NC_000005.10:g.111074642_111074648del
GRCh38.p14 chr 5	NC_000005.10:g.111074643_111074648del
GRCh38.p14 chr 5	NC_000005.10:g.111074644_111074648del
GRCh38.p14 chr 5	NC_000005.10:g.111074645_111074648del
GRCh38.p14 chr 5	NC_000005.10:g.111074646_111074648del
GRCh38.p14 chr 5	NC_000005.10:g.111074647_111074648del
GRCh38.p14 chr 5	NC_000005.10:g.111074648del
GRCh38.p14 chr 5	NC_000005.10:g.111074648dup
GRCh38.p14 chr 5	NC_000005.10:g.111074647_111074648dup
GRCh38.p14 chr 5	NC_000005.10:g.111074646_111074648dup
GRCh38.p14 chr 5	NC_000005.10:g.111074645_111074648dup
GRCh38.p14 chr 5	NC_000005.10:g.111074644_111074648dup
GRCh38.p14 chr 5	NC_000005.10:g.111074643_111074648dup
GRCh38.p14 chr 5	NC_000005.10:g.111074648_111074649insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 5	NC_000005.9:g.110410335_110410346del
GRCh37.p13 chr 5	NC_000005.9:g.110410338_110410346del
GRCh37.p13 chr 5	NC_000005.9:g.110410340_110410346del
GRCh37.p13 chr 5	NC_000005.9:g.110410341_110410346del
GRCh37.p13 chr 5	NC_000005.9:g.110410342_110410346del
GRCh37.p13 chr 5	NC_000005.9:g.110410343_110410346del
GRCh37.p13 chr 5	NC_000005.9:g.110410344_110410346del
GRCh37.p13 chr 5	NC_000005.9:g.110410345_110410346del
GRCh37.p13 chr 5	NC_000005.9:g.110410346del
GRCh37.p13 chr 5	NC_000005.9:g.110410346dup
GRCh37.p13 chr 5	NC_000005.9:g.110410345_110410346dup
GRCh37.p13 chr 5	NC_000005.9:g.110410344_110410346dup
GRCh37.p13 chr 5	NC_000005.9:g.110410343_110410346dup
GRCh37.p13 chr 5	NC_000005.9:g.110410342_110410346dup
GRCh37.p13 chr 5	NC_000005.9:g.110410341_110410346dup
GRCh37.p13 chr 5	NC_000005.9:g.110410346_110410347insTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: TSLP, thymic stromal lymphopoietin (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TSLP transcript variant 1	NM_033035.5:c.351+992_351… NM_033035.5:c.351+992_351+1003del	N/A	Intron Variant
TSLP transcript variant 2	NM_138551.5:c.63+992_63+1… NM_138551.5:c.63+992_63+1003del	N/A	Intron Variant
TSLP transcript variant 3	NR_045089.2:n.	N/A	Intron Variant
TSLP transcript variant X3	XM_011543698.2:c.63+992_6… XM_011543698.2:c.63+992_63+1003del	N/A	Intron Variant
TSLP transcript variant X1	XM_047417846.1:c.321+992_… XM_047417846.1:c.321+992_321+1003del	N/A	Intron Variant
TSLP transcript variant X2	XM_047417847.1:c.189+992_… XM_047417847.1:c.189+992_189+1003del	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₁=	del(T)₁₂	del(T)₉	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	ins(T)₂₆
GRCh38.p14 chr 5	NC_000005.10:g.111074628_111074648=	NC_000005.10:g.111074637_111074648del	NC_000005.10:g.111074640_111074648del	NC_000005.10:g.111074642_111074648del	NC_000005.10:g.111074643_111074648del	NC_000005.10:g.111074644_111074648del	NC_000005.10:g.111074645_111074648del	NC_000005.10:g.111074646_111074648del	NC_000005.10:g.111074647_111074648del	NC_000005.10:g.111074648del	NC_000005.10:g.111074648dup	NC_000005.10:g.111074647_111074648dup	NC_000005.10:g.111074646_111074648dup	NC_000005.10:g.111074645_111074648dup	NC_000005.10:g.111074644_111074648dup	NC_000005.10:g.111074643_111074648dup	NC_000005.10:g.111074648_111074649insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 5	NC_000005.9:g.110410326_110410346=	NC_000005.9:g.110410335_110410346del	NC_000005.9:g.110410338_110410346del	NC_000005.9:g.110410340_110410346del	NC_000005.9:g.110410341_110410346del	NC_000005.9:g.110410342_110410346del	NC_000005.9:g.110410343_110410346del	NC_000005.9:g.110410344_110410346del	NC_000005.9:g.110410345_110410346del	NC_000005.9:g.110410346del	NC_000005.9:g.110410346dup	NC_000005.9:g.110410345_110410346dup	NC_000005.9:g.110410344_110410346dup	NC_000005.9:g.110410343_110410346dup	NC_000005.9:g.110410342_110410346dup	NC_000005.9:g.110410341_110410346dup	NC_000005.9:g.110410346_110410347insTTTTTTTTTTTTTTTTTTTTTTTTTT
TSLP transcript variant 1	NM_033035.4:c.351+983=	NM_033035.4:c.351+992_351+1003del	NM_033035.4:c.351+995_351+1003del	NM_033035.4:c.351+997_351+1003del	NM_033035.4:c.351+998_351+1003del	NM_033035.4:c.351+999_351+1003del	NM_033035.4:c.351+1000_351+1003del	NM_033035.4:c.351+1001_351+1003del	NM_033035.4:c.351+1002_351+1003del	NM_033035.4:c.351+1003del	NM_033035.4:c.351+1003dup	NM_033035.4:c.351+1002_351+1003dup	NM_033035.4:c.351+1001_351+1003dup	NM_033035.4:c.351+1000_351+1003dup	NM_033035.4:c.351+999_351+1003dup	NM_033035.4:c.351+998_351+1003dup	NM_033035.4:c.351+1003_351+1004insTTTTTTTTTTTTTTTTTTTTTTTTTT
TSLP transcript variant 1	NM_033035.5:c.351+983=	NM_033035.5:c.351+992_351+1003del	NM_033035.5:c.351+995_351+1003del	NM_033035.5:c.351+997_351+1003del	NM_033035.5:c.351+998_351+1003del	NM_033035.5:c.351+999_351+1003del	NM_033035.5:c.351+1000_351+1003del	NM_033035.5:c.351+1001_351+1003del	NM_033035.5:c.351+1002_351+1003del	NM_033035.5:c.351+1003del	NM_033035.5:c.351+1003dup	NM_033035.5:c.351+1002_351+1003dup	NM_033035.5:c.351+1001_351+1003dup	NM_033035.5:c.351+1000_351+1003dup	NM_033035.5:c.351+999_351+1003dup	NM_033035.5:c.351+998_351+1003dup	NM_033035.5:c.351+1003_351+1004insTTTTTTTTTTTTTTTTTTTTTTTTTT
TSLP transcript variant 2	NM_138551.4:c.63+983=	NM_138551.4:c.63+992_63+1003del	NM_138551.4:c.63+995_63+1003del	NM_138551.4:c.63+997_63+1003del	NM_138551.4:c.63+998_63+1003del	NM_138551.4:c.63+999_63+1003del	NM_138551.4:c.63+1000_63+1003del	NM_138551.4:c.63+1001_63+1003del	NM_138551.4:c.63+1002_63+1003del	NM_138551.4:c.63+1003del	NM_138551.4:c.63+1003dup	NM_138551.4:c.63+1002_63+1003dup	NM_138551.4:c.63+1001_63+1003dup	NM_138551.4:c.63+1000_63+1003dup	NM_138551.4:c.63+999_63+1003dup	NM_138551.4:c.63+998_63+1003dup	NM_138551.4:c.63+1003_63+1004insTTTTTTTTTTTTTTTTTTTTTTTTTT
TSLP transcript variant 2	NM_138551.5:c.63+983=	NM_138551.5:c.63+992_63+1003del	NM_138551.5:c.63+995_63+1003del	NM_138551.5:c.63+997_63+1003del	NM_138551.5:c.63+998_63+1003del	NM_138551.5:c.63+999_63+1003del	NM_138551.5:c.63+1000_63+1003del	NM_138551.5:c.63+1001_63+1003del	NM_138551.5:c.63+1002_63+1003del	NM_138551.5:c.63+1003del	NM_138551.5:c.63+1003dup	NM_138551.5:c.63+1002_63+1003dup	NM_138551.5:c.63+1001_63+1003dup	NM_138551.5:c.63+1000_63+1003dup	NM_138551.5:c.63+999_63+1003dup	NM_138551.5:c.63+998_63+1003dup	NM_138551.5:c.63+1003_63+1004insTTTTTTTTTTTTTTTTTTTTTTTTTT
TSLP transcript variant X3	XM_011543698.2:c.63+983=	XM_011543698.2:c.63+992_63+1003del	XM_011543698.2:c.63+995_63+1003del	XM_011543698.2:c.63+997_63+1003del	XM_011543698.2:c.63+998_63+1003del	XM_011543698.2:c.63+999_63+1003del	XM_011543698.2:c.63+1000_63+1003del	XM_011543698.2:c.63+1001_63+1003del	XM_011543698.2:c.63+1002_63+1003del	XM_011543698.2:c.63+1003del	XM_011543698.2:c.63+1003dup	XM_011543698.2:c.63+1002_63+1003dup	XM_011543698.2:c.63+1001_63+1003dup	XM_011543698.2:c.63+1000_63+1003dup	XM_011543698.2:c.63+999_63+1003dup	XM_011543698.2:c.63+998_63+1003dup	XM_011543698.2:c.63+1003_63+1004insTTTTTTTTTTTTTTTTTTTTTTTTTT
TSLP transcript variant X1	XM_047417846.1:c.321+983=	XM_047417846.1:c.321+992_321+1003del	XM_047417846.1:c.321+995_321+1003del	XM_047417846.1:c.321+997_321+1003del	XM_047417846.1:c.321+998_321+1003del	XM_047417846.1:c.321+999_321+1003del	XM_047417846.1:c.321+1000_321+1003del	XM_047417846.1:c.321+1001_321+1003del	XM_047417846.1:c.321+1002_321+1003del	XM_047417846.1:c.321+1003del	XM_047417846.1:c.321+1003dup	XM_047417846.1:c.321+1002_321+1003dup	XM_047417846.1:c.321+1001_321+1003dup	XM_047417846.1:c.321+1000_321+1003dup	XM_047417846.1:c.321+999_321+1003dup	XM_047417846.1:c.321+998_321+1003dup	XM_047417846.1:c.321+1003_321+1004insTTTTTTTTTTTTTTTTTTTTTTTTTT
TSLP transcript variant X2	XM_047417847.1:c.189+983=	XM_047417847.1:c.189+992_189+1003del	XM_047417847.1:c.189+995_189+1003del	XM_047417847.1:c.189+997_189+1003del	XM_047417847.1:c.189+998_189+1003del	XM_047417847.1:c.189+999_189+1003del	XM_047417847.1:c.189+1000_189+1003del	XM_047417847.1:c.189+1001_189+1003del	XM_047417847.1:c.189+1002_189+1003del	XM_047417847.1:c.189+1003del	XM_047417847.1:c.189+1003dup	XM_047417847.1:c.189+1002_189+1003dup	XM_047417847.1:c.189+1001_189+1003dup	XM_047417847.1:c.189+1000_189+1003dup	XM_047417847.1:c.189+999_189+1003dup	XM_047417847.1:c.189+998_189+1003dup	XM_047417847.1:c.189+1003_189+1004insTTTTTTTTTTTTTTTTTTTTTTTTTT

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, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42637427	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss95403726	Dec 05, 2013 (138)
3	PJP	ss295239604	May 09, 2011 (137)
4	PJP	ss295239605	May 09, 2011 (134)
5	SSMP	ss663549037	Apr 01, 2015 (144)
6	1000GENOMES	ss1374299896	Aug 21, 2014 (142)
7	EVA_UK10K_ALSPAC	ss1704816148	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1704816150	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1704816207	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1704816208	Apr 01, 2015 (144)
11	SWEGEN	ss2997543656	Nov 08, 2017 (151)
12	URBANLAB	ss3648138219	Oct 12, 2018 (152)
13	PACBIO	ss3785209780	Jul 13, 2019 (153)
14	PACBIO	ss3790599771	Jul 13, 2019 (153)
15	PACBIO	ss3795476550	Jul 13, 2019 (153)
16	KHV_HUMAN_GENOMES	ss3807045589	Jul 13, 2019 (153)
17	EVA	ss3829426969	Apr 26, 2020 (154)
18	GNOMAD	ss4126644875	Apr 26, 2021 (155)
19	GNOMAD	ss4126644876	Apr 26, 2021 (155)
20	GNOMAD	ss4126644877	Apr 26, 2021 (155)
21	GNOMAD	ss4126644878	Apr 26, 2021 (155)
22	GNOMAD	ss4126644879	Apr 26, 2021 (155)
23	GNOMAD	ss4126644880	Apr 26, 2021 (155)
24	GNOMAD	ss4126644881	Apr 26, 2021 (155)
25	GNOMAD	ss4126644882	Apr 26, 2021 (155)
26	GNOMAD	ss4126644883	Apr 26, 2021 (155)
27	GNOMAD	ss4126644884	Apr 26, 2021 (155)
28	GNOMAD	ss4126644885	Apr 26, 2021 (155)
29	GNOMAD	ss4126644886	Apr 26, 2021 (155)
30	GNOMAD	ss4126644887	Apr 26, 2021 (155)
31	GNOMAD	ss4126644888	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5173454359	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5173454360	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5173454361	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5173454362	Apr 26, 2021 (155)
36	1000G_HIGH_COVERAGE	ss5265298001	Oct 13, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5265298002	Oct 13, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5265298003	Oct 13, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5265298004	Oct 13, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5265298005	Oct 13, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5265298006	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5463323602	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5463323603	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5463323604	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5463323605	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5463323606	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5710336921	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5710336922	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5710336923	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5710336924	Oct 13, 2022 (156)
51	EVA	ss5835432053	Oct 13, 2022 (156)
52	EVA	ss5835432054	Oct 13, 2022 (156)
53	1000Genomes	NC_000005.9 - 110410326	Oct 12, 2018 (152)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 15706556 (NC_000005.9:110410325::TT 1242/3854) Row 15706557 (NC_000005.9:110410325::T 1340/3854)	-	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 15706556 (NC_000005.9:110410325::TT 1242/3854) Row 15706557 (NC_000005.9:110410325::T 1340/3854)	-	Oct 12, 2018 (152)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 199845206 (NC_000005.10:111074627::T 38770/101762) Row 199845207 (NC_000005.10:111074627::TT 1830/101708) Row 199845208 (NC_000005.10:111074627::TTT 183/101732)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 31423666 (NC_000005.9:110410325::T 5715/16574) Row 31423667 (NC_000005.9:110410325:T: 308/16574) Row 31423668 (NC_000005.9:110410325::TT 243/16574)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 31423666 (NC_000005.9:110410325::T 5715/16574) Row 31423667 (NC_000005.9:110410325:T: 308/16574) Row 31423668 (NC_000005.9:110410325::TT 243/16574)...	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 31423666 (NC_000005.9:110410325::T 5715/16574) Row 31423667 (NC_000005.9:110410325:T: 308/16574) Row 31423668 (NC_000005.9:110410325::TT 243/16574)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 31423666 (NC_000005.9:110410325::T 5715/16574) Row 31423667 (NC_000005.9:110410325:T: 308/16574) Row 31423668 (NC_000005.9:110410325::TT 243/16574)...	-	Apr 26, 2021 (155)
74	14KJPN Submission ignored due to conflicting rows: Row 44174025 (NC_000005.10:111074627::TT 396/28210) Row 44174026 (NC_000005.10:111074627::T 10066/28210) Row 44174027 (NC_000005.10:111074627:T: 626/28210)...	-	Oct 13, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 44174025 (NC_000005.10:111074627::TT 396/28210) Row 44174026 (NC_000005.10:111074627::T 10066/28210) Row 44174027 (NC_000005.10:111074627:T: 626/28210)...	-	Oct 13, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 44174025 (NC_000005.10:111074627::TT 396/28210) Row 44174026 (NC_000005.10:111074627::T 10066/28210) Row 44174027 (NC_000005.10:111074627:T: 626/28210)...	-	Oct 13, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 44174025 (NC_000005.10:111074627::TT 396/28210) Row 44174026 (NC_000005.10:111074627::T 10066/28210) Row 44174027 (NC_000005.10:111074627:T: 626/28210)...	-	Oct 13, 2022 (156)
78	UK 10K study - Twins Submission ignored due to conflicting rows: Row 15706556 (NC_000005.9:110410325::TT 1111/3708) Row 15706557 (NC_000005.9:110410325::T 1242/3708)	-	Oct 12, 2018 (152)
79	UK 10K study - Twins Submission ignored due to conflicting rows: Row 15706556 (NC_000005.9:110410325::TT 1111/3708) Row 15706557 (NC_000005.9:110410325::T 1242/3708)	-	Oct 12, 2018 (152)
80	ALFA	NC_000005.10 - 111074628	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)
rs67913511	Feb 27, 2009 (130)
rs71969921	May 11, 2012 (137)
rs144047032	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4126644888	NC_000005.10:111074627:TTTTTTTTT:	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4126644887	NC_000005.10:111074627:TTTTTTT:	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5173454362	NC_000005.9:110410325:TTTTTT:	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5710336924	NC_000005.10:111074627:TTTTTT:	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT
ss4126644886, ss5265298006	NC_000005.10:111074627:TTTTT:	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4126644885	NC_000005.10:111074627:TTTT:	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4126644884, ss5265298005, ss5463323606	NC_000005.10:111074627:TTT:	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4126644883, ss5463323605	NC_000005.10:111074627:TT:	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss295239605	NC_000005.8:110438244:T:	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss2997543656, ss3785209780, ss3790599771, ss3795476550, ss3829426969, ss5173454360	NC_000005.9:110410325:T:	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4126644882, ss5265298002, ss5463323604, ss5710336923	NC_000005.10:111074627:T:	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss295239604	NC_000005.8:110438225::T	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
28249122, ss663549037, ss1374299896, ss1704816150, ss1704816208, ss5173454359	NC_000005.9:110410325::T	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3648138219, ss3807045589, ss4126644875, ss5265298001, ss5463323602, ss5710336922	NC_000005.10:111074627::T	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss42637427, ss95403726	NT_034772.6:18724218::T	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss1704816148, ss1704816207, ss5173454361, ss5835432053	NC_000005.9:110410325::TT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4126644876, ss5265298003, ss5463323603, ss5710336921	NC_000005.10:111074627::TT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5835432054	NC_000005.9:110410325::TTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
ss4126644877, ss5265298004	NC_000005.10:111074627::TTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4126644878	NC_000005.10:111074627::TTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4126644879	NC_000005.10:111074627::TTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4126644880	NC_000005.10:111074627::TTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10424352235	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4126644881	NC_000005.10:111074627::TTTTTTTTTT… NC_000005.10:111074627::TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:111074627:TTTTTTTTTTT… NC_000005.10:111074627:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs35180980

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

rs35180980