Name: rs59158357
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.

rs59158357

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:145885098-145885122 (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(GT)₆ / del(GT)₅ / del(GT)₃ / d…
del(GT)₆ / del(GT)₅ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅ / dup(GT)₆ / dup(GT)₇ / dup(GT)₈ / dup(GT)₉ / dup(GT)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: delGTGT=0.000975 (258/264690, TOPMED)
dupGT=0.14629 (1637/11190, ALFA)
dupGT=0.4245 (2126/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GRXCR2 : 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	11190	TGTGTGTGTGTGTGTGTGTGTGTGT=0.84879	TGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGT=0.00009, TGTGTGTGTGTGTGTGTGTGTGT=0.00063, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.14629, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00420, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00000	0.760108	0.053249	0.186643	32
European	Sub	9856	TGTGTGTGTGTGTGTGTGTGTGTGT=0.8286	TGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0001, TGTGTGTGTGTGTGTGTGTGTGT=0.0007, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1658, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0048, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.727683	0.060332	0.211984	32
African	Sub	912	TGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	34	TGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	878	TGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	12	TGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	10	TGTGTGTGTGTGTGTGTGTGTGTGT=1.0	TGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TGTGTGTGTGTGTGTGTGTGTGTGT=1.0	TGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	62	TGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	138	TGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	24	TGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other	Sub	186	TGTGTGTGTGTGTGTGTGTGTGTGT=0.984	TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.016, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	0.978495	0.010753	0.010753	22

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	(TG)₁₂T=0.999025	delGTGT=0.000975
Allele Frequency Aggregator	Total	Global	11190	(TG)₁₂T=0.84879	del(GT)₆=0.00000, del(GT)₅=0.00000, del(GT)₃=0.00000, delGTGT=0.00009, delGT=0.00063, dupGT=0.14629, dupGTGT=0.00420, dup(GT)₃=0.00000, dup(GT)₄=0.00000, dup(GT)₅=0.00000, dup(GT)₆=0.00000, dup(GT)₇=0.00000, dup(GT)₈=0.00000, dup(GT)₁₀=0.00000
Allele Frequency Aggregator	European	Sub	9856	(TG)₁₂T=0.8286	del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₃=0.0000, delGTGT=0.0001, delGT=0.0007, dupGT=0.1658, dupGTGT=0.0048, dup(GT)₃=0.0000, dup(GT)₄=0.0000, dup(GT)₅=0.0000, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₁₀=0.0000
Allele Frequency Aggregator	African	Sub	912	(TG)₁₂T=1.000	del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₁₀=0.000
Allele Frequency Aggregator	Other	Sub	186	(TG)₁₂T=0.984	del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.016, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₁₀=0.000
Allele Frequency Aggregator	Latin American 2	Sub	138	(TG)₁₂T=1.000	del(GT)₆=0.000, del(GT)₅=0.000, del(GT)₃=0.000, delGTGT=0.000, delGT=0.000, dupGT=0.000, dupGTGT=0.000, dup(GT)₃=0.000, dup(GT)₄=0.000, dup(GT)₅=0.000, dup(GT)₆=0.000, dup(GT)₇=0.000, dup(GT)₈=0.000, dup(GT)₁₀=0.000
Allele Frequency Aggregator	Latin American 1	Sub	62	(TG)₁₂T=1.00	del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₁₀=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(TG)₁₂T=1.00	del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₁₀=0.00
Allele Frequency Aggregator	Asian	Sub	12	(TG)₁₂T=1.00	del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₁₀=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupGT=0.4245
1000Genomes	African	Sub	1322	- No frequency provided	dupGT=0.3328
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupGT=0.5923
1000Genomes	Europe	Sub	1006	- No frequency provided	dupGT=0.2932
1000Genomes	South Asian	Sub	978	- No frequency provided	dupGT=0.515
1000Genomes	American	Sub	694	- No frequency provided	dupGT=0.418

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.145885099GT[6]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[7]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[9]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[10]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[11]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[13]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[14]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[15]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[16]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[17]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[18]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[19]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[20]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[21]
GRCh38.p14 chr 5	NC_000005.10:g.145885099GT[22]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[6]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[7]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[9]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[10]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[11]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[13]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[14]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[15]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[16]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[17]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[18]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[19]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[20]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[21]
GRCh37.p13 chr 5	NC_000005.9:g.145264662GT[22]

Gene: GRXCR2, glutaredoxin and cysteine rich domain containing 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GRXCR2 transcript	NM_001080516.2:c.	N/A	Genic Upstream Transcript Variant
GRXCR2 transcript variant X1	XM_017009708.2:c.49-18393… XM_017009708.2:c.49-18393CA[6]	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	(TG)₁₂T=	del(GT)₆	del(GT)₅	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅	dup(GT)₆	dup(GT)₇	dup(GT)₈	dup(GT)₉	dup(GT)₁₀
GRCh38.p14 chr 5	NC_000005.10:g.145885098_145885122=	NC_000005.10:g.145885099GT[6]	NC_000005.10:g.145885099GT[7]	NC_000005.10:g.145885099GT[9]	NC_000005.10:g.145885099GT[10]	NC_000005.10:g.145885099GT[11]	NC_000005.10:g.145885099GT[13]	NC_000005.10:g.145885099GT[14]	NC_000005.10:g.145885099GT[15]	NC_000005.10:g.145885099GT[16]	NC_000005.10:g.145885099GT[17]	NC_000005.10:g.145885099GT[18]	NC_000005.10:g.145885099GT[19]	NC_000005.10:g.145885099GT[20]	NC_000005.10:g.145885099GT[21]	NC_000005.10:g.145885099GT[22]
GRCh37.p13 chr 5	NC_000005.9:g.145264661_145264685=	NC_000005.9:g.145264662GT[6]	NC_000005.9:g.145264662GT[7]	NC_000005.9:g.145264662GT[9]	NC_000005.9:g.145264662GT[10]	NC_000005.9:g.145264662GT[11]	NC_000005.9:g.145264662GT[13]	NC_000005.9:g.145264662GT[14]	NC_000005.9:g.145264662GT[15]	NC_000005.9:g.145264662GT[16]	NC_000005.9:g.145264662GT[17]	NC_000005.9:g.145264662GT[18]	NC_000005.9:g.145264662GT[19]	NC_000005.9:g.145264662GT[20]	NC_000005.9:g.145264662GT[21]	NC_000005.9:g.145264662GT[22]
GRXCR2 transcript variant X1	XM_005268496.1:c.-59-12071=	XM_005268496.1:c.-59-12094CA[6]	XM_005268496.1:c.-59-12094CA[7]	XM_005268496.1:c.-59-12094CA[9]	XM_005268496.1:c.-59-12094CA[10]	XM_005268496.1:c.-59-12094CA[11]	XM_005268496.1:c.-59-12094CA[13]	XM_005268496.1:c.-59-12094CA[14]	XM_005268496.1:c.-59-12094CA[15]	XM_005268496.1:c.-59-12094CA[16]	XM_005268496.1:c.-59-12094CA[17]	XM_005268496.1:c.-59-12094CA[18]	XM_005268496.1:c.-59-12094CA[19]	XM_005268496.1:c.-59-12094CA[20]	XM_005268496.1:c.-59-12094CA[21]	XM_005268496.1:c.-59-12094CA[22]
GRXCR2 transcript variant X1	XM_017009708.2:c.49-18370=	XM_017009708.2:c.49-18393CA[6]	XM_017009708.2:c.49-18393CA[7]	XM_017009708.2:c.49-18393CA[9]	XM_017009708.2:c.49-18393CA[10]	XM_017009708.2:c.49-18393CA[11]	XM_017009708.2:c.49-18393CA[13]	XM_017009708.2:c.49-18393CA[14]	XM_017009708.2:c.49-18393CA[15]	XM_017009708.2:c.49-18393CA[16]	XM_017009708.2:c.49-18393CA[17]	XM_017009708.2:c.49-18393CA[18]	XM_017009708.2:c.49-18393CA[19]	XM_017009708.2:c.49-18393CA[20]	XM_017009708.2:c.49-18393CA[21]	XM_017009708.2:c.49-18393CA[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#.

80 SubSNP, 38 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81636413	Dec 04, 2013 (138)
2	HGSV	ss81795156	Dec 04, 2013 (138)
3	HGSV	ss82124317	Dec 03, 2013 (138)
4	HUMANGENOME_JCVI	ss95949097	Dec 05, 2013 (138)
5	BCMHGSC_JDW	ss103892064	Dec 06, 2013 (138)
6	GMI	ss288663638	May 04, 2012 (137)
7	1000GENOMES	ss326729060	May 09, 2011 (134)
8	1000GENOMES	ss326773669	May 09, 2011 (134)
9	LUNTER	ss551551841	Apr 25, 2013 (138)
10	LUNTER	ss553220544	Apr 25, 2013 (138)
11	1000GENOMES	ss1374628805	Aug 21, 2014 (142)
12	DDI	ss1536482614	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1704907327	Jan 10, 2018 (151)
14	EVA_UK10K_TWINSUK	ss1704907626	Jan 10, 2018 (151)
15	EVA_UK10K_TWINSUK	ss1710235541	Oct 12, 2018 (152)
16	EVA_UK10K_ALSPAC	ss1710235542	Oct 12, 2018 (152)
17	SWEGEN	ss2997949869	Jan 10, 2018 (151)
18	MCHAISSO	ss3066046991	Nov 08, 2017 (151)
19	URBANLAB	ss3648189820	Oct 12, 2018 (152)
20	EVA_DECODE	ss3715891193	Jul 13, 2019 (153)
21	EVA_DECODE	ss3715891194	Jul 13, 2019 (153)
22	EVA_DECODE	ss3715891195	Jul 13, 2019 (153)
23	EVA_DECODE	ss3715891196	Jul 13, 2019 (153)
24	EVA_DECODE	ss3715891197	Jul 13, 2019 (153)
25	EVA_DECODE	ss3715891198	Jul 13, 2019 (153)
26	ACPOP	ss3732898823	Jul 13, 2019 (153)
27	ACPOP	ss3732898824	Jul 13, 2019 (153)
28	PACBIO	ss3785275053	Jul 13, 2019 (153)
29	PACBIO	ss3790653922	Jul 13, 2019 (153)
30	PACBIO	ss3795530907	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3807350573	Jul 13, 2019 (153)
32	EVA	ss3829550860	Apr 26, 2020 (154)
33	EVA	ss3838249816	Apr 26, 2020 (154)
34	EVA	ss3843692752	Apr 26, 2020 (154)
35	KOGIC	ss3957834751	Apr 26, 2020 (154)
36	KOGIC	ss3957834752	Apr 26, 2020 (154)
37	KOGIC	ss3957834753	Apr 26, 2020 (154)
38	KOGIC	ss3957834754	Apr 26, 2020 (154)
39	GNOMAD	ss4131114370	Apr 26, 2021 (155)
40	GNOMAD	ss4131114371	Apr 26, 2021 (155)
41	GNOMAD	ss4131114372	Apr 26, 2021 (155)
42	GNOMAD	ss4131114373	Apr 26, 2021 (155)
43	GNOMAD	ss4131114374	Apr 26, 2021 (155)
44	GNOMAD	ss4131114375	Apr 26, 2021 (155)
45	GNOMAD	ss4131114376	Apr 26, 2021 (155)
46	GNOMAD	ss4131114377	Apr 26, 2021 (155)
47	GNOMAD	ss4131114378	Apr 26, 2021 (155)
48	GNOMAD	ss4131114379	Apr 26, 2021 (155)
49	GNOMAD	ss4131114381	Apr 26, 2021 (155)
50	GNOMAD	ss4131114382	Apr 26, 2021 (155)
51	GNOMAD	ss4131114383	Apr 26, 2021 (155)
52	GNOMAD	ss4131114384	Apr 26, 2021 (155)
53	GNOMAD	ss4131114385	Apr 26, 2021 (155)
54	TOPMED	ss4682196550	Apr 26, 2021 (155)
55	TOMMO_GENOMICS	ss5174590948	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5174590949	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5174590950	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5174590951	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5174590952	Apr 26, 2021 (155)
60	1000G_HIGH_COVERAGE	ss5266188597	Oct 17, 2022 (156)
61	1000G_HIGH_COVERAGE	ss5266188598	Oct 17, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5266188599	Oct 17, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5266188600	Oct 17, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5266188601	Oct 17, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5266188602	Oct 17, 2022 (156)
66	HUGCELL_USP	ss5464118036	Oct 17, 2022 (156)
67	HUGCELL_USP	ss5464118037	Oct 17, 2022 (156)
68	HUGCELL_USP	ss5464118038	Oct 17, 2022 (156)
69	HUGCELL_USP	ss5464118039	Oct 17, 2022 (156)
70	HUGCELL_USP	ss5464118040	Oct 17, 2022 (156)
71	HUGCELL_USP	ss5464118041	Oct 17, 2022 (156)
72	TOMMO_GENOMICS	ss5711801334	Oct 17, 2022 (156)
73	TOMMO_GENOMICS	ss5711801335	Oct 17, 2022 (156)
74	TOMMO_GENOMICS	ss5711801337	Oct 17, 2022 (156)
75	TOMMO_GENOMICS	ss5711801338	Oct 17, 2022 (156)
76	TOMMO_GENOMICS	ss5711801339	Oct 17, 2022 (156)
77	EVA	ss5835775158	Oct 17, 2022 (156)
78	EVA	ss5835775159	Oct 17, 2022 (156)
79	EVA	ss5835775160	Oct 17, 2022 (156)
80	EVA	ss5855055136	Oct 17, 2022 (156)
81	1000Genomes	NC_000005.9 - 145264661	Oct 12, 2018 (152)
82	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 16303617 (NC_000005.9:145264660:TG: 323/3854) Row 16303618 (NC_000005.9:145264660::TG 1151/3854)	-	Oct 12, 2018 (152)
83	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 16303617 (NC_000005.9:145264660:TG: 323/3854) Row 16303618 (NC_000005.9:145264660::TG 1151/3854)	-	Oct 12, 2018 (152)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207295670 (NC_000005.10:145885097::TG 46483/135874) Row 207295671 (NC_000005.10:145885097::TGTG 4708/135974) Row 207295672 (NC_000005.10:145885097::TGTGTG 1477/135980)...	-	Apr 26, 2021 (155)
99	Korean Genome Project Submission ignored due to conflicting rows: Row 14212752 (NC_000005.10:145885101::TG 1135/1832) Row 14212753 (NC_000005.10:145885099:TG: 9/1832) Row 14212754 (NC_000005.10:145885101::TGTG 36/1832)...	-	Apr 26, 2020 (154)
100	Korean Genome Project Submission ignored due to conflicting rows: Row 14212752 (NC_000005.10:145885101::TG 1135/1832) Row 14212753 (NC_000005.10:145885099:TG: 9/1832) Row 14212754 (NC_000005.10:145885101::TGTG 36/1832)...	-	Apr 26, 2020 (154)
101	Korean Genome Project Submission ignored due to conflicting rows: Row 14212752 (NC_000005.10:145885101::TG 1135/1832) Row 14212753 (NC_000005.10:145885099:TG: 9/1832) Row 14212754 (NC_000005.10:145885101::TGTG 36/1832)...	-	Apr 26, 2020 (154)
102	Korean Genome Project Submission ignored due to conflicting rows: Row 14212752 (NC_000005.10:145885101::TG 1135/1832) Row 14212753 (NC_000005.10:145885099:TG: 9/1832) Row 14212754 (NC_000005.10:145885101::TGTG 36/1832)...	-	Apr 26, 2020 (154)
103	Northern Sweden Submission ignored due to conflicting rows: Row 6183688 (NC_000005.9:145264660::TG 201/600) Row 6183689 (NC_000005.9:145264660::TGTG 1/600)	-	Jul 13, 2019 (153)
104	Northern Sweden Submission ignored due to conflicting rows: Row 6183688 (NC_000005.9:145264660::TG 201/600) Row 6183689 (NC_000005.9:145264660::TGTG 1/600)	-	Jul 13, 2019 (153)
105	8.3KJPN Submission ignored due to conflicting rows: Row 32560255 (NC_000005.9:145264660::TG 11239/16760) Row 32560256 (NC_000005.9:145264660:TG: 13/16760) Row 32560257 (NC_000005.9:145264660::TGTG 225/16760)...	-	Apr 26, 2021 (155)
106	8.3KJPN Submission ignored due to conflicting rows: Row 32560255 (NC_000005.9:145264660::TG 11239/16760) Row 32560256 (NC_000005.9:145264660:TG: 13/16760) Row 32560257 (NC_000005.9:145264660::TGTG 225/16760)...	-	Apr 26, 2021 (155)
107	8.3KJPN Submission ignored due to conflicting rows: Row 32560255 (NC_000005.9:145264660::TG 11239/16760) Row 32560256 (NC_000005.9:145264660:TG: 13/16760) Row 32560257 (NC_000005.9:145264660::TGTG 225/16760)...	-	Apr 26, 2021 (155)
108	8.3KJPN Submission ignored due to conflicting rows: Row 32560255 (NC_000005.9:145264660::TG 11239/16760) Row 32560256 (NC_000005.9:145264660:TG: 13/16760) Row 32560257 (NC_000005.9:145264660::TGTG 225/16760)...	-	Apr 26, 2021 (155)
109	8.3KJPN Submission ignored due to conflicting rows: Row 32560255 (NC_000005.9:145264660::TG 11239/16760) Row 32560256 (NC_000005.9:145264660:TG: 13/16760) Row 32560257 (NC_000005.9:145264660::TGTG 225/16760)...	-	Apr 26, 2021 (155)
110	14KJPN Submission ignored due to conflicting rows: Row 45638438 (NC_000005.10:145885097::TG 19008/28258) Row 45638439 (NC_000005.10:145885097::TGTG 386/28258) Row 45638441 (NC_000005.10:145885097:TG: 16/28258)...	-	Oct 17, 2022 (156)
111	14KJPN Submission ignored due to conflicting rows: Row 45638438 (NC_000005.10:145885097::TG 19008/28258) Row 45638439 (NC_000005.10:145885097::TGTG 386/28258) Row 45638441 (NC_000005.10:145885097:TG: 16/28258)...	-	Oct 17, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 45638438 (NC_000005.10:145885097::TG 19008/28258) Row 45638439 (NC_000005.10:145885097::TGTG 386/28258) Row 45638441 (NC_000005.10:145885097:TG: 16/28258)...	-	Oct 17, 2022 (156)
113	14KJPN Submission ignored due to conflicting rows: Row 45638438 (NC_000005.10:145885097::TG 19008/28258) Row 45638439 (NC_000005.10:145885097::TGTG 386/28258) Row 45638441 (NC_000005.10:145885097:TG: 16/28258)...	-	Oct 17, 2022 (156)
114	14KJPN Submission ignored due to conflicting rows: Row 45638438 (NC_000005.10:145885097::TG 19008/28258) Row 45638439 (NC_000005.10:145885097::TGTG 386/28258) Row 45638441 (NC_000005.10:145885097:TG: 16/28258)...	-	Oct 17, 2022 (156)
115	TopMed	NC_000005.10 - 145885098	Apr 26, 2021 (155)
116	UK 10K study - Twins Submission ignored due to conflicting rows: Row 16303617 (NC_000005.9:145264660:TG: 326/3708) Row 16303618 (NC_000005.9:145264660::TG 1035/3708)	-	Oct 12, 2018 (152)
117	UK 10K study - Twins Submission ignored due to conflicting rows: Row 16303617 (NC_000005.9:145264660:TG: 326/3708) Row 16303618 (NC_000005.9:145264660::TG 1035/3708)	-	Oct 12, 2018 (152)
118	ALFA	NC_000005.10 - 145885098	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)
rs796570085	Nov 08, 2017 (151)
rs67343229	May 15, 2013 (138)
rs67343230	Feb 27, 2009 (130)
rs67343231	Feb 27, 2009 (130)
rs67343232	Feb 27, 2009 (130)
rs142981054	Jul 30, 2012 (137)
rs371462464	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4131114385	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTG:	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT	(self)
ss4131114384	NC_000005.10:145885097:TGTGTGTGTG:	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss4131114383	NC_000005.10:145885097:TGTGTG:	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT	(self)
ss5174590952	NC_000005.9:145264660:TGTG:	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
519574107, ss3715891193, ss3957834754, ss4131114382, ss4682196550, ss5711801339	NC_000005.10:145885097:TGTG:	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss1704907327, ss1704907626, ss2997949869, ss5174590949, ss5835775160	NC_000005.9:145264660:TG:	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4131114381, ss5711801337	NC_000005.10:145885097:TG:	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3715891194, ss3957834752	NC_000005.10:145885099:TG:	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss326729060, ss326773669, ss551551841, ss553220544	NC_000005.8:145244853::TG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss288663638	NC_000005.8:145244878::GT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
29303841, ss1374628805, ss1536482614, ss3732898823, ss3785275053, ss3790653922, ss3795530907, ss3838249816, ss5174590948, ss5835775158	NC_000005.9:145264660::TG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss1710235541, ss1710235542	NC_000005.9:145264662::TG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3807350573, ss3843692752, ss4131114370, ss5266188597, ss5464118036, ss5711801334, ss5855055136	NC_000005.10:145885097::TG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3715891195, ss3957834751	NC_000005.10:145885101::TG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss81636413, ss81795156, ss82124317, ss103892064	NT_029289.11:6427612::GT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3732898824, ss3829550860, ss5174590950, ss5835775159	NC_000005.9:145264660::TGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4131114371, ss5266188600, ss5464118037, ss5711801335	NC_000005.10:145885097::TGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3715891196, ss3957834753	NC_000005.10:145885101::TGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3648189820	NC_000005.10:145885121::TGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss95949097	NT_029289.11:6427612::GTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5174590951	NC_000005.9:145264660::TGTGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4131114372, ss5266188601, ss5464118038, ss5711801338	NC_000005.10:145885097::TGTGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3715891197	NC_000005.10:145885101::TGTGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3066046991, ss4131114373, ss5266188598, ss5464118040	NC_000005.10:145885097::TGTGTGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4131114374, ss5266188602, ss5464118039	NC_000005.10:145885097::TGTGTGTGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4131114375, ss5266188599, ss5464118041	NC_000005.10:145885097::TGTGTGTGTG… NC_000005.10:145885097::TGTGTGTGTGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3715891198	NC_000005.10:145885101::TGTGTGTGTG… NC_000005.10:145885101::TGTGTGTGTGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4131114376	NC_000005.10:145885097::TGTGTGTGTG… NC_000005.10:145885097::TGTGTGTGTGTGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4131114377	NC_000005.10:145885097::TGTGTGTGTG… NC_000005.10:145885097::TGTGTGTGTGTGTGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4131114378	NC_000005.10:145885097::TGTGTGTGTG… NC_000005.10:145885097::TGTGTGTGTGTGTGTGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4131114379	NC_000005.10:145885097::TGTGTGTGTG… NC_000005.10:145885097::TGTGTGTGTGTGTGTGTGTG	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
4706117667	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000005.10:145885097:TGTGTGTGTGT… NC_000005.10:145885097:TGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(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 rs59158357

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

rs59158357