Name: rs35486965
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.

rs35486965

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:17838713-17838733 (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)₉ / del(T)₈ / del(T)₆ / del(…
del(T)₉ / del(T)₈ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / ins(T)₂₂
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₉=0.000019 (5/264690, TOPMED)
dupT=0.03087 (347/11240, ALFA)
delT=0.15 (6/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: JAK3 : 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	11240	TTTTTTTTTTTTTTTTTTTTT=0.94733	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00044, TTTTTTTTTTTTTTTTTTTTTT=0.03087, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.02037, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00080, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00018, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.948855	0.010155	0.04099	32
European	Sub	9928	TTTTTTTTTTTTTTTTTTTTT=0.9406	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTTT=0.0348, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0231, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.942227	0.011555	0.046218	32
African	Sub	448	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	8	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	440	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	52	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	36	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	60	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	416	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	60	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	276	TTTTTTTTTTTTTTTTTTTTT=0.993	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.007, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.985507	0.0	0.014493	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(T)₂₁=0.999981	del(T)₉=0.000019
Allele Frequency Aggregator	Total	Global	11240	(T)₂₁=0.94733	del(T)₉=0.00000, del(T)₈=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00044, dupT=0.03087, dupTT=0.00000, dupTTT=0.02037, dup(T)₄=0.00080, dup(T)₅=0.00000, ins(T)₂₂=0.00018
Allele Frequency Aggregator	European	Sub	9928	(T)₂₁=0.9406	del(T)₉=0.0000, del(T)₈=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0005, dupT=0.0348, dupTT=0.0000, dupTTT=0.0231, dup(T)₄=0.0009, dup(T)₅=0.0000, ins(T)₂₂=0.0002
Allele Frequency Aggregator	African	Sub	448	(T)₂₁=1.000	del(T)₉=0.000, del(T)₈=0.000, del(T)₆=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)₅=0.000, ins(T)₂₂=0.000
Allele Frequency Aggregator	Latin American 2	Sub	416	(T)₂₁=1.000	del(T)₉=0.000, del(T)₈=0.000, del(T)₆=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)₅=0.000, ins(T)₂₂=0.000
Allele Frequency Aggregator	Other	Sub	276	(T)₂₁=0.993	del(T)₉=0.000, del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.007, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, ins(T)₂₂=0.000
Allele Frequency Aggregator	Latin American 1	Sub	60	(T)₂₁=1.00	del(T)₉=0.00, del(T)₈=0.00, del(T)₆=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)₅=0.00, ins(T)₂₂=0.00
Allele Frequency Aggregator	South Asian	Sub	60	(T)₂₁=1.00	del(T)₉=0.00, del(T)₈=0.00, del(T)₆=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)₅=0.00, ins(T)₂₂=0.00
Allele Frequency Aggregator	Asian	Sub	52	(T)₂₁=1.00	del(T)₉=0.00, del(T)₈=0.00, del(T)₆=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)₅=0.00, ins(T)₂₂=0.00
The Danish reference pan genome	Danish	Study-wide	40	(T)₂₁=0.85	delT=0.15

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 19	NC_000019.10:g.17838725_17838733del
GRCh38.p14 chr 19	NC_000019.10:g.17838726_17838733del
GRCh38.p14 chr 19	NC_000019.10:g.17838728_17838733del
GRCh38.p14 chr 19	NC_000019.10:g.17838729_17838733del
GRCh38.p14 chr 19	NC_000019.10:g.17838730_17838733del
GRCh38.p14 chr 19	NC_000019.10:g.17838731_17838733del
GRCh38.p14 chr 19	NC_000019.10:g.17838732_17838733del
GRCh38.p14 chr 19	NC_000019.10:g.17838733del
GRCh38.p14 chr 19	NC_000019.10:g.17838733dup
GRCh38.p14 chr 19	NC_000019.10:g.17838732_17838733dup
GRCh38.p14 chr 19	NC_000019.10:g.17838731_17838733dup
GRCh38.p14 chr 19	NC_000019.10:g.17838730_17838733dup
GRCh38.p14 chr 19	NC_000019.10:g.17838729_17838733dup
GRCh38.p14 chr 19	NC_000019.10:g.17838728_17838733dup
GRCh38.p14 chr 19	NC_000019.10:g.17838727_17838733dup
GRCh38.p14 chr 19	NC_000019.10:g.17838733_17838734insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.17949534_17949542del
GRCh37.p13 chr 19	NC_000019.9:g.17949535_17949542del
GRCh37.p13 chr 19	NC_000019.9:g.17949537_17949542del
GRCh37.p13 chr 19	NC_000019.9:g.17949538_17949542del
GRCh37.p13 chr 19	NC_000019.9:g.17949539_17949542del
GRCh37.p13 chr 19	NC_000019.9:g.17949540_17949542del
GRCh37.p13 chr 19	NC_000019.9:g.17949541_17949542del
GRCh37.p13 chr 19	NC_000019.9:g.17949542del
GRCh37.p13 chr 19	NC_000019.9:g.17949542dup
GRCh37.p13 chr 19	NC_000019.9:g.17949541_17949542dup
GRCh37.p13 chr 19	NC_000019.9:g.17949540_17949542dup
GRCh37.p13 chr 19	NC_000019.9:g.17949539_17949542dup
GRCh37.p13 chr 19	NC_000019.9:g.17949538_17949542dup
GRCh37.p13 chr 19	NC_000019.9:g.17949537_17949542dup
GRCh37.p13 chr 19	NC_000019.9:g.17949536_17949542dup
GRCh37.p13 chr 19	NC_000019.9:g.17949542_17949543insTTTTTTTTTTTTTTTTTTTTTT
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14271_14279del
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14272_14279del
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14274_14279del
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14275_14279del
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14276_14279del
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14277_14279del
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14278_14279del
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14279del
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14279dup
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14278_14279dup
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14277_14279dup
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14276_14279dup
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14275_14279dup
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14274_14279dup
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14273_14279dup
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14279_14280insAAAAAAAAAAAAAAAAAAAAAA

Gene: JAK3, Janus kinase 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
JAK3 transcript	NM_000215.4:c.1442-331_14… NM_000215.4:c.1442-331_1442-323del	N/A	Intron Variant
JAK3 transcript variant X3	XM_011527991.3:c.1442-331… XM_011527991.3:c.1442-331_1442-323del	N/A	Intron Variant
JAK3 transcript variant X1	XM_047438786.1:c.1442-331… XM_047438786.1:c.1442-331_1442-323del	N/A	Intron Variant
JAK3 transcript variant X2	XR_007066796.1:n.	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)₉	del(T)₈	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	ins(T)₂₂
GRCh38.p14 chr 19	NC_000019.10:g.17838713_17838733=	NC_000019.10:g.17838725_17838733del	NC_000019.10:g.17838726_17838733del	NC_000019.10:g.17838728_17838733del	NC_000019.10:g.17838729_17838733del	NC_000019.10:g.17838730_17838733del	NC_000019.10:g.17838731_17838733del	NC_000019.10:g.17838732_17838733del	NC_000019.10:g.17838733del	NC_000019.10:g.17838733dup	NC_000019.10:g.17838732_17838733dup	NC_000019.10:g.17838731_17838733dup	NC_000019.10:g.17838730_17838733dup	NC_000019.10:g.17838729_17838733dup	NC_000019.10:g.17838728_17838733dup	NC_000019.10:g.17838727_17838733dup	NC_000019.10:g.17838733_17838734insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.17949522_17949542=	NC_000019.9:g.17949534_17949542del	NC_000019.9:g.17949535_17949542del	NC_000019.9:g.17949537_17949542del	NC_000019.9:g.17949538_17949542del	NC_000019.9:g.17949539_17949542del	NC_000019.9:g.17949540_17949542del	NC_000019.9:g.17949541_17949542del	NC_000019.9:g.17949542del	NC_000019.9:g.17949542dup	NC_000019.9:g.17949541_17949542dup	NC_000019.9:g.17949540_17949542dup	NC_000019.9:g.17949539_17949542dup	NC_000019.9:g.17949538_17949542dup	NC_000019.9:g.17949537_17949542dup	NC_000019.9:g.17949536_17949542dup	NC_000019.9:g.17949542_17949543insTTTTTTTTTTTTTTTTTTTTTT
JAK3 RefSeqGene (LRG_77)	NG_007273.1:g.14259_14279=	NG_007273.1:g.14271_14279del	NG_007273.1:g.14272_14279del	NG_007273.1:g.14274_14279del	NG_007273.1:g.14275_14279del	NG_007273.1:g.14276_14279del	NG_007273.1:g.14277_14279del	NG_007273.1:g.14278_14279del	NG_007273.1:g.14279del	NG_007273.1:g.14279dup	NG_007273.1:g.14278_14279dup	NG_007273.1:g.14277_14279dup	NG_007273.1:g.14276_14279dup	NG_007273.1:g.14275_14279dup	NG_007273.1:g.14274_14279dup	NG_007273.1:g.14273_14279dup	NG_007273.1:g.14279_14280insAAAAAAAAAAAAAAAAAAAAAA
JAK3 transcript	NM_000215.3:c.1442-323=	NM_000215.3:c.1442-331_1442-323del	NM_000215.3:c.1442-330_1442-323del	NM_000215.3:c.1442-328_1442-323del	NM_000215.3:c.1442-327_1442-323del	NM_000215.3:c.1442-326_1442-323del	NM_000215.3:c.1442-325_1442-323del	NM_000215.3:c.1442-324_1442-323del	NM_000215.3:c.1442-323del	NM_000215.3:c.1442-323dup	NM_000215.3:c.1442-324_1442-323dup	NM_000215.3:c.1442-325_1442-323dup	NM_000215.3:c.1442-326_1442-323dup	NM_000215.3:c.1442-327_1442-323dup	NM_000215.3:c.1442-328_1442-323dup	NM_000215.3:c.1442-329_1442-323dup	NM_000215.3:c.1442-323_1442-322insAAAAAAAAAAAAAAAAAAAAAA
JAK3 transcript	NM_000215.4:c.1442-323=	NM_000215.4:c.1442-331_1442-323del	NM_000215.4:c.1442-330_1442-323del	NM_000215.4:c.1442-328_1442-323del	NM_000215.4:c.1442-327_1442-323del	NM_000215.4:c.1442-326_1442-323del	NM_000215.4:c.1442-325_1442-323del	NM_000215.4:c.1442-324_1442-323del	NM_000215.4:c.1442-323del	NM_000215.4:c.1442-323dup	NM_000215.4:c.1442-324_1442-323dup	NM_000215.4:c.1442-325_1442-323dup	NM_000215.4:c.1442-326_1442-323dup	NM_000215.4:c.1442-327_1442-323dup	NM_000215.4:c.1442-328_1442-323dup	NM_000215.4:c.1442-329_1442-323dup	NM_000215.4:c.1442-323_1442-322insAAAAAAAAAAAAAAAAAAAAAA
JAK3 transcript variant X1	XM_005259896.1:c.1571-323=	XM_005259896.1:c.1571-331_1571-323del	XM_005259896.1:c.1571-330_1571-323del	XM_005259896.1:c.1571-328_1571-323del	XM_005259896.1:c.1571-327_1571-323del	XM_005259896.1:c.1571-326_1571-323del	XM_005259896.1:c.1571-325_1571-323del	XM_005259896.1:c.1571-324_1571-323del	XM_005259896.1:c.1571-323del	XM_005259896.1:c.1571-323dup	XM_005259896.1:c.1571-324_1571-323dup	XM_005259896.1:c.1571-325_1571-323dup	XM_005259896.1:c.1571-326_1571-323dup	XM_005259896.1:c.1571-327_1571-323dup	XM_005259896.1:c.1571-328_1571-323dup	XM_005259896.1:c.1571-329_1571-323dup	XM_005259896.1:c.1571-323_1571-322insAAAAAAAAAAAAAAAAAAAAAA
JAK3 transcript variant X3	XM_011527991.3:c.1442-323=	XM_011527991.3:c.1442-331_1442-323del	XM_011527991.3:c.1442-330_1442-323del	XM_011527991.3:c.1442-328_1442-323del	XM_011527991.3:c.1442-327_1442-323del	XM_011527991.3:c.1442-326_1442-323del	XM_011527991.3:c.1442-325_1442-323del	XM_011527991.3:c.1442-324_1442-323del	XM_011527991.3:c.1442-323del	XM_011527991.3:c.1442-323dup	XM_011527991.3:c.1442-324_1442-323dup	XM_011527991.3:c.1442-325_1442-323dup	XM_011527991.3:c.1442-326_1442-323dup	XM_011527991.3:c.1442-327_1442-323dup	XM_011527991.3:c.1442-328_1442-323dup	XM_011527991.3:c.1442-329_1442-323dup	XM_011527991.3:c.1442-323_1442-322insAAAAAAAAAAAAAAAAAAAAAA
JAK3 transcript variant X1	XM_047438786.1:c.1442-323=	XM_047438786.1:c.1442-331_1442-323del	XM_047438786.1:c.1442-330_1442-323del	XM_047438786.1:c.1442-328_1442-323del	XM_047438786.1:c.1442-327_1442-323del	XM_047438786.1:c.1442-326_1442-323del	XM_047438786.1:c.1442-325_1442-323del	XM_047438786.1:c.1442-324_1442-323del	XM_047438786.1:c.1442-323del	XM_047438786.1:c.1442-323dup	XM_047438786.1:c.1442-324_1442-323dup	XM_047438786.1:c.1442-325_1442-323dup	XM_047438786.1:c.1442-326_1442-323dup	XM_047438786.1:c.1442-327_1442-323dup	XM_047438786.1:c.1442-328_1442-323dup	XM_047438786.1:c.1442-329_1442-323dup	XM_047438786.1:c.1442-323_1442-322insAAAAAAAAAAAAAAAAAAAAAA

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#.

43 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40975744	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95723735	Dec 05, 2013 (138)
3	PJP	ss294956199	May 09, 2011 (137)
4	EVA_GENOME_DK	ss1575250598	Apr 01, 2015 (144)
5	SWEGEN	ss3017199775	Nov 08, 2017 (151)
6	GNOMAD	ss4328648077	Apr 27, 2021 (155)
7	GNOMAD	ss4328648078	Apr 27, 2021 (155)
8	GNOMAD	ss4328648079	Apr 27, 2021 (155)
9	GNOMAD	ss4328648080	Apr 27, 2021 (155)
10	GNOMAD	ss4328648082	Apr 27, 2021 (155)
11	GNOMAD	ss4328648083	Apr 27, 2021 (155)
12	GNOMAD	ss4328648084	Apr 27, 2021 (155)
13	GNOMAD	ss4328648085	Apr 27, 2021 (155)
14	GNOMAD	ss4328648086	Apr 27, 2021 (155)
15	GNOMAD	ss4328648087	Apr 27, 2021 (155)
16	GNOMAD	ss4328648088	Apr 27, 2021 (155)
17	GNOMAD	ss4328648089	Apr 27, 2021 (155)
18	GNOMAD	ss4328648090	Apr 27, 2021 (155)
19	GNOMAD	ss4328648091	Apr 27, 2021 (155)
20	TOPMED	ss5069848386	Apr 27, 2021 (155)
21	TOMMO_GENOMICS	ss5227033211	Apr 27, 2021 (155)
22	TOMMO_GENOMICS	ss5227033212	Apr 27, 2021 (155)
23	TOMMO_GENOMICS	ss5227033213	Apr 27, 2021 (155)
24	TOMMO_GENOMICS	ss5227033214	Apr 27, 2021 (155)
25	TOMMO_GENOMICS	ss5227033215	Apr 27, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5306708844	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5306708845	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5306708846	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5306708847	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5306708848	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5306708849	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5499308721	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5499308722	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5499308723	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5499308724	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5499308725	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5499308726	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5785415187	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5785415188	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5785415189	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5785415190	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5785415191	Oct 16, 2022 (156)
43	EVA	ss5852227894	Oct 16, 2022 (156)
44	The Danish reference pan genome	NC_000019.9 - 17949522	Apr 27, 2020 (154)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 535739047 (NC_000019.10:17838712::T 17216/90516) Row 535739048 (NC_000019.10:17838712::TT 556/90634) Row 535739049 (NC_000019.10:17838712::TTT 5910/90580)...	-	Apr 27, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 85002518 (NC_000019.9:17949521::T 2463/16636) Row 85002519 (NC_000019.9:17949521::TTT 2356/16636) Row 85002520 (NC_000019.9:17949521:T: 56/16636)...	-	Apr 27, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 85002518 (NC_000019.9:17949521::T 2463/16636) Row 85002519 (NC_000019.9:17949521::TTT 2356/16636) Row 85002520 (NC_000019.9:17949521:T: 56/16636)...	-	Apr 27, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 85002518 (NC_000019.9:17949521::T 2463/16636) Row 85002519 (NC_000019.9:17949521::TTT 2356/16636) Row 85002520 (NC_000019.9:17949521:T: 56/16636)...	-	Apr 27, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 85002518 (NC_000019.9:17949521::T 2463/16636) Row 85002519 (NC_000019.9:17949521::TTT 2356/16636) Row 85002520 (NC_000019.9:17949521:T: 56/16636)...	-	Apr 27, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 85002518 (NC_000019.9:17949521::T 2463/16636) Row 85002519 (NC_000019.9:17949521::TTT 2356/16636) Row 85002520 (NC_000019.9:17949521:T: 56/16636)...	-	Apr 27, 2021 (155)
64	14KJPN Submission ignored due to conflicting rows: Row 119252291 (NC_000019.10:17838712::T 4169/27792) Row 119252292 (NC_000019.10:17838712::TTT 3475/27792) Row 119252293 (NC_000019.10:17838712:T: 85/27792)...	-	Oct 16, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 119252291 (NC_000019.10:17838712::T 4169/27792) Row 119252292 (NC_000019.10:17838712::TTT 3475/27792) Row 119252293 (NC_000019.10:17838712:T: 85/27792)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 119252291 (NC_000019.10:17838712::T 4169/27792) Row 119252292 (NC_000019.10:17838712::TTT 3475/27792) Row 119252293 (NC_000019.10:17838712:T: 85/27792)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 119252291 (NC_000019.10:17838712::T 4169/27792) Row 119252292 (NC_000019.10:17838712::TTT 3475/27792) Row 119252293 (NC_000019.10:17838712:T: 85/27792)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 119252291 (NC_000019.10:17838712::T 4169/27792) Row 119252292 (NC_000019.10:17838712::TTT 3475/27792) Row 119252293 (NC_000019.10:17838712:T: 85/27792)...	-	Oct 16, 2022 (156)
69	TopMed	NC_000019.10 - 17838713	Apr 27, 2021 (155)
70	ALFA	NC_000019.10 - 17838713	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs72295058	May 11, 2012 (137)
rs150851247	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
285394050, ss4328648091, ss5069848386	NC_000019.10:17838712:TTTTTTTTT:	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4328648090	NC_000019.10:17838712:TTTTTTTT:	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4328648089	NC_000019.10:17838712:TTTTTT:	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4328648088	NC_000019.10:17838712:TTTT:	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3017199775	NC_000019.9:17949521:TTT:	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4328648087, ss5306708845, ss5499308726	NC_000019.10:17838712:TTT:	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4328648086, ss5306708848, ss5499308721	NC_000019.10:17838712:TT:	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
624142, ss1575250598, ss5227033213	NC_000019.9:17949521:T:	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4328648085, ss5499308725, ss5785415189, ss5852227894	NC_000019.10:17838712:T:	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss294956199	NC_000019.8:17810522::T	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5227033211	NC_000019.9:17949521::T	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4328648077, ss5306708844, ss5499308722, ss5785415187	NC_000019.10:17838712::T	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss40975744	NT_011295.11:9212323::T	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss95723735	NT_011295.11:9212344::T	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5227033215	NC_000019.9:17949521::TT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4328648078, ss5306708849, ss5785415191	NC_000019.10:17838712::TT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5227033212	NC_000019.9:17949521::TTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4328648079, ss5306708847, ss5499308723, ss5785415188	NC_000019.10:17838712::TTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5227033214	NC_000019.9:17949521::TTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4328648080, ss5306708846, ss5499308724, ss5785415190	NC_000019.10:17838712::TTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4328648082	NC_000019.10:17838712::TTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4328648083	NC_000019.10:17838712::TTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4328648084	NC_000019.10:17838712::TTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6659794669	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:17838712:TTTTTTTTTTTT… NC_000019.10:17838712:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs35486965

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

rs35486965