Name: rs1491492011
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.

rs1491492011

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:407965-407966 (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: insC / insCCC / insCCCA(C)₄ / insC…
insC / insCCC / insCCCA(C)₄ / insCCCA(C)₄GCCTCGCGG(C)₅GG(C)₄ / ins(C)₄ / ins(C)₄AGG(C)₄ / ins(C)₆(G)₄CC / ins(C)₅G(C)₅ / ins(CCCCCG)₂G(C)₄ / ins(C)₅(GCCCC)₂CGG(C)₄ / ins(C)₅GGCACC / ins(C)₅GG(C)₄ / ins(C)₅GG(C)₄G(C)₅GG(C)₄ / ins(CCCCCGGCCCCG)₂(C)₅GG(C)₄ / ins(CCCCCGGCCCCG)₃(C)₅GG(C)₄ / ins(C)₅GG(CCCCG)₂G(C)₄ / ins(C)₅GT(C)₄ / ins(C)₄GC / ins(C)₄G(C)₄ / ins(C)₄G(C)₆ / ins(CCCCGCC)₂CC / ins(C)₄G(C)₆GG(C)₄GCCCA(C)₄GCCTCGCGG(C)₄ / ins(C)₄G(C)₆GG(C)₄GCCCA(C)₄GCCTCGCG(GCCCCCGGCCCC)₂ / ins(C)₄G(C)₆GG(C)₄GCCCA(C)₄GCCTCGCG(GCCCCCGGCCCC)₂GCCCA(C)₄GCCTCGCG(GCCCCCG)₂(GCCCC)₂(CGGCCCCGCCCCGCCCCC)₂CGG(C)₄G(C)₅GG(C)₄ / ins(C)₄G(C)₆GG(C)₄G(C)₅GG(C)₄ / ins(C)₄G(C)₅GG(C)₄ / ins(CCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGG)₂(C)₄G(C)₅GG(C)₄ / ins(CCCCG)₂(C)₆GG(C)₄GCCCA(C)₄GCCTCGCG(GCCCCCGGCCCC)₂ / ins(CCCCG)₂(C)₅GG(C)₄ / ins(C)₄G(C)₄TCGG(C)₄ / ins(C)₄GG(C)₄ / ins(C)₄GG(C)₅ / ins(CCCCGGC)₂CCCG(C)₅GG(C)₄ / ins(C)₄T(C)₄ / insT(C)₄GG(C)₄
Variation Type: Insertion
Frequency: insC=0.00000 (0/10726, ALFA)
insCCC=0.00000 (0/10726, ALFA)
ins(C)₄=0.00000 (0/10726, ALFA) (+ 9 more)
ins(C)₄AGG(C)₄=0.00000 (0/10726, ALFA)
ins(C)₅G(C)₅=0.00000 (0/10726, ALFA)
ins(C)₅(GCCCC)₂CGG(C)₄=0.00000 (0/10726, ALFA)
ins(C)₅GGCACC=0.00000 (0/10726, ALFA)
ins(C)₅GG(C)₄=0.00000 (0/10726, ALFA)
ins(C)₅GG(C)₄G(C)₅GG(C)₄=0.00000 (0/10726, ALFA)
ins(C)₅GT(C)₄=0.00000 (0/10726, ALFA)
ins(C)₄GG(C)₄=0.00000 (0/10726, ALFA)
ins(C)₄GG(C)₅=0.00000 (0/10726, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RBCK1 : 2KB Upstream Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	10726	=1.00000	C=0.00000, CCC=0.00000, CCCC=0.00000, CCCCAGGCCCC=0.00000, CCCCCGCCCCC=0.00000, CCCCCGCCCCGCCCCCGGCCCC=0.00000, CCCCCGGCACC=0.00000, CCCCCGGCCCC=0.00000, CCCCCGGCCCCGCCCCCGGCCCC=0.00000, CCCCCGTCCCC=0.00000, CCCCGGCCCC=0.00000, CCCCGGCCCCC=0.00000	1.0	N/A
European	Sub	6858	=1.0000	C=0.0000, CCC=0.0000, CCCC=0.0000, CCCCAGGCCCC=0.0000, CCCCCGCCCCC=0.0000, CCCCCGCCCCGCCCCCGGCCCC=0.0000, CCCCCGGCACC=0.0000, CCCCCGGCCCC=0.0000, CCCCCGGCCCCGCCCCCGGCCCC=0.0000, CCCCCGTCCCC=0.0000, CCCCGGCCCC=0.0000, CCCCGGCCCCC=0.0000	1.0	N/A
African	Sub	2606	=1.0000	C=0.0000, CCC=0.0000, CCCC=0.0000, CCCCAGGCCCC=0.0000, CCCCCGCCCCC=0.0000, CCCCCGCCCCGCCCCCGGCCCC=0.0000, CCCCCGGCACC=0.0000, CCCCCGGCCCC=0.0000, CCCCCGGCCCCGCCCCCGGCCCC=0.0000, CCCCCGTCCCC=0.0000, CCCCGGCCCC=0.0000, CCCCGGCCCCC=0.0000	1.0	N/A
African Others	Sub	104	=1.000	C=0.000, CCC=0.000, CCCC=0.000, CCCCAGGCCCC=0.000, CCCCCGCCCCC=0.000, CCCCCGCCCCGCCCCCGGCCCC=0.000, CCCCCGGCACC=0.000, CCCCCGGCCCC=0.000, CCCCCGGCCCCGCCCCCGGCCCC=0.000, CCCCCGTCCCC=0.000, CCCCGGCCCC=0.000, CCCCGGCCCCC=0.000	1.0	N/A
African American	Sub	2502	=1.0000	C=0.0000, CCC=0.0000, CCCC=0.0000, CCCCAGGCCCC=0.0000, CCCCCGCCCCC=0.0000, CCCCCGCCCCGCCCCCGGCCCC=0.0000, CCCCCGGCACC=0.0000, CCCCCGGCCCC=0.0000, CCCCCGGCCCCGCCCCCGGCCCC=0.0000, CCCCCGTCCCC=0.0000, CCCCGGCCCC=0.0000, CCCCGGCCCCC=0.0000	1.0	N/A
Asian	Sub	86	=1.00	C=0.00, CCC=0.00, CCCC=0.00, CCCCAGGCCCC=0.00, CCCCCGCCCCC=0.00, CCCCCGCCCCGCCCCCGGCCCC=0.00, CCCCCGGCACC=0.00, CCCCCGGCCCC=0.00, CCCCCGGCCCCGCCCCCGGCCCC=0.00, CCCCCGTCCCC=0.00, CCCCGGCCCC=0.00, CCCCGGCCCCC=0.00	1.0	N/A
East Asian	Sub	68	=1.00	C=0.00, CCC=0.00, CCCC=0.00, CCCCAGGCCCC=0.00, CCCCCGCCCCC=0.00, CCCCCGCCCCGCCCCCGGCCCC=0.00, CCCCCGGCACC=0.00, CCCCCGGCCCC=0.00, CCCCCGGCCCCGCCCCCGGCCCC=0.00, CCCCCGTCCCC=0.00, CCCCGGCCCC=0.00, CCCCGGCCCCC=0.00	1.0	N/A
Other Asian	Sub	18	=1.00	C=0.00, CCC=0.00, CCCC=0.00, CCCCAGGCCCC=0.00, CCCCCGCCCCC=0.00, CCCCCGCCCCGCCCCCGGCCCC=0.00, CCCCCGGCACC=0.00, CCCCCGGCCCC=0.00, CCCCCGGCCCCGCCCCCGGCCCC=0.00, CCCCCGTCCCC=0.00, CCCCGGCCCC=0.00, CCCCGGCCCCC=0.00	1.0	N/A
Latin American 1	Sub	132	=1.000	C=0.000, CCC=0.000, CCCC=0.000, CCCCAGGCCCC=0.000, CCCCCGCCCCC=0.000, CCCCCGCCCCGCCCCCGGCCCC=0.000, CCCCCGGCACC=0.000, CCCCCGGCCCC=0.000, CCCCCGGCCCCGCCCCCGGCCCC=0.000, CCCCCGTCCCC=0.000, CCCCGGCCCC=0.000, CCCCGGCCCCC=0.000	1.0	N/A
Latin American 2	Sub	576	=1.000	C=0.000, CCC=0.000, CCCC=0.000, CCCCAGGCCCC=0.000, CCCCCGCCCCC=0.000, CCCCCGCCCCGCCCCCGGCCCC=0.000, CCCCCGGCACC=0.000, CCCCCGGCCCC=0.000, CCCCCGGCCCCGCCCCCGGCCCC=0.000, CCCCCGTCCCC=0.000, CCCCGGCCCC=0.000, CCCCGGCCCCC=0.000	1.0	N/A
South Asian	Sub	62	=1.00	C=0.00, CCC=0.00, CCCC=0.00, CCCCAGGCCCC=0.00, CCCCCGCCCCC=0.00, CCCCCGCCCCGCCCCCGGCCCC=0.00, CCCCCGGCACC=0.00, CCCCCGGCCCC=0.00, CCCCCGGCCCCGCCCCCGGCCCC=0.00, CCCCCGTCCCC=0.00, CCCCGGCCCC=0.00, CCCCGGCCCCC=0.00	1.0	N/A
Other	Sub	406	=1.000	C=0.000, CCC=0.000, CCCC=0.000, CCCCAGGCCCC=0.000, CCCCCGCCCCC=0.000, CCCCCGCCCCGCCCCCGGCCCC=0.000, CCCCCGGCACC=0.000, CCCCCGGCCCC=0.000, CCCCCGGCCCCGCCCCCGGCCCC=0.000, CCCCCGTCCCC=0.000, CCCCGGCCCC=0.000, CCCCGGCCCCC=0.000	1.0	N/A

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

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	10726	- No frequency provided	insC=0.00000, insCCC=0.00000, ins(C)₄=0.00000, ins(C)₄AGG(C)₄=0.00000, ins(C)₅G(C)₅=0.00000, ins(C)₅(GCCCC)₂CGG(C)₄=0.00000, ins(C)₅GGCACC=0.00000, ins(C)₅GG(C)₄=0.00000, ins(C)₅GG(C)₄G(C)₅GG(C)₄=0.00000, ins(C)₅GT(C)₄=0.00000, ins(C)₄GG(C)₄=0.00000, ins(C)₄GG(C)₅=0.00000
Allele Frequency Aggregator	European	Sub	6858	- No frequency provided	insC=0.0000, insCCC=0.0000, ins(C)₄=0.0000, ins(C)₄AGG(C)₄=0.0000, ins(C)₅G(C)₅=0.0000, ins(C)₅(GCCCC)₂CGG(C)₄=0.0000, ins(C)₅GGCACC=0.0000, ins(C)₅GG(C)₄=0.0000, ins(C)₅GG(C)₄G(C)₅GG(C)₄=0.0000, ins(C)₅GT(C)₄=0.0000, ins(C)₄GG(C)₄=0.0000, ins(C)₄GG(C)₅=0.0000
Allele Frequency Aggregator	African	Sub	2606	- No frequency provided	insC=0.0000, insCCC=0.0000, ins(C)₄=0.0000, ins(C)₄AGG(C)₄=0.0000, ins(C)₅G(C)₅=0.0000, ins(C)₅(GCCCC)₂CGG(C)₄=0.0000, ins(C)₅GGCACC=0.0000, ins(C)₅GG(C)₄=0.0000, ins(C)₅GG(C)₄G(C)₅GG(C)₄=0.0000, ins(C)₅GT(C)₄=0.0000, ins(C)₄GG(C)₄=0.0000, ins(C)₄GG(C)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	576	- No frequency provided	insC=0.000, insCCC=0.000, ins(C)₄=0.000, ins(C)₄AGG(C)₄=0.000, ins(C)₅G(C)₅=0.000, ins(C)₅(GCCCC)₂CGG(C)₄=0.000, ins(C)₅GGCACC=0.000, ins(C)₅GG(C)₄=0.000, ins(C)₅GG(C)₄G(C)₅GG(C)₄=0.000, ins(C)₅GT(C)₄=0.000, ins(C)₄GG(C)₄=0.000, ins(C)₄GG(C)₅=0.000
Allele Frequency Aggregator	Other	Sub	406	- No frequency provided	insC=0.000, insCCC=0.000, ins(C)₄=0.000, ins(C)₄AGG(C)₄=0.000, ins(C)₅G(C)₅=0.000, ins(C)₅(GCCCC)₂CGG(C)₄=0.000, ins(C)₅GGCACC=0.000, ins(C)₅GG(C)₄=0.000, ins(C)₅GG(C)₄G(C)₅GG(C)₄=0.000, ins(C)₅GT(C)₄=0.000, ins(C)₄GG(C)₄=0.000, ins(C)₄GG(C)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	132	- No frequency provided	insC=0.000, insCCC=0.000, ins(C)₄=0.000, ins(C)₄AGG(C)₄=0.000, ins(C)₅G(C)₅=0.000, ins(C)₅(GCCCC)₂CGG(C)₄=0.000, ins(C)₅GGCACC=0.000, ins(C)₅GG(C)₄=0.000, ins(C)₅GG(C)₄G(C)₅GG(C)₄=0.000, ins(C)₅GT(C)₄=0.000, ins(C)₄GG(C)₄=0.000, ins(C)₄GG(C)₅=0.000
Allele Frequency Aggregator	Asian	Sub	86	- No frequency provided	insC=0.00, insCCC=0.00, ins(C)₄=0.00, ins(C)₄AGG(C)₄=0.00, ins(C)₅G(C)₅=0.00, ins(C)₅(GCCCC)₂CGG(C)₄=0.00, ins(C)₅GGCACC=0.00, ins(C)₅GG(C)₄=0.00, ins(C)₅GG(C)₄G(C)₅GG(C)₄=0.00, ins(C)₅GT(C)₄=0.00, ins(C)₄GG(C)₄=0.00, ins(C)₄GG(C)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	62	- No frequency provided	insC=0.00, insCCC=0.00, ins(C)₄=0.00, ins(C)₄AGG(C)₄=0.00, ins(C)₅G(C)₅=0.00, ins(C)₅(GCCCC)₂CGG(C)₄=0.00, ins(C)₅GGCACC=0.00, ins(C)₅GG(C)₄=0.00, ins(C)₅GG(C)₄G(C)₅GG(C)₄=0.00, ins(C)₅GT(C)₄=0.00, ins(C)₄GG(C)₄=0.00, ins(C)₄GG(C)₅=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCACCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCACCCCGCCTCGCGGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCAGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCCCGGGGCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCCGCCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCCGCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCCGGCACC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCCGGCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCCGGCCCCGCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCCGTCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCCCCGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCCCCGGCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGCCCCTCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGGCCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCGGCCCCCGGCCCCGCCCCCGGCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insCCCCTCCCC
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966insTCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCACCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCACCCCGCCTCGCGGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCAGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCCCGGGGCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCCGCCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCCGCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCCGGCACC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCCGGCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCCGGCCCCGCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCCGTCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCCCCGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCCCCGGCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGCCCCTCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGGCCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCGGCCCCCGGCCCCGCCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insCCCCTCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610insTCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCACCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCACCCCGCCTCGCGGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCAGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCCCGGGGCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCCGCCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCCGCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCCGGCACC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCCGGCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCCGGCCCCGCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCCGTCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCCCCGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCCCCGGCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGCCCCTCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGGCCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCGGCCCCCGGCCCCGCCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insCCCCTCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902insTCCCCGGCCCC

Gene: RBCK1, RANBP2-type and C3HC4-type zinc finger containing 1 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
RBCK1 transcript variant 3	NM_001323956.2:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant 4	NM_001323958.2:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant 5	NM_001323960.2:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant 1	NM_006462.6:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant 2	NM_031229.4:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant 6	NR_136659.2:n.	N/A	Upstream Transcript Variant
RBCK1 transcript variant X3	XM_005260645.3:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant X1	XM_011529137.3:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant X2	XM_011529138.2:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant X3	XM_011529139.4:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant X4	XM_011529140.3:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant X5	XM_047439833.1:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant X6	XM_047439834.1:c.	N/A	Upstream Transcript Variant
RBCK1 transcript variant X7	XM_047439835.1:c.	N/A	Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	=	insC	insCCC	insCCCA(C)₄	insCCCA(C)₄GCCTCGCGG(C)₅GG(C)₄	ins(C)₄	ins(C)₄AGG(C)₄	ins(C)₆(G)₄CC	ins(C)₅G(C)₅	ins(CCCCCG)₂G(C)₄	ins(C)₅(GCCCC)₂CGG(C)₄	ins(C)₅GGCACC	ins(C)₅GG(C)₄	ins(C)₅GG(C)₄G(C)₅GG(C)₄	ins(CCCCCGGCCCCG)₂(C)₅GG(C)₄	ins(CCCCCGGCCCCG)₃(C)₅GG(C)₄	ins(C)₅GG(CCCCG)₂G(C)₄	ins(C)₅GT(C)₄	ins(C)₄GC	ins(C)₄G(C)₄	ins(C)₄G(C)₆	ins(CCCCGCC)₂CC	ins(C)₄G(C)₆GG(C)₄GCCCA(C)₄GCCTCGCGG(C)₄	ins(C)₄G(C)₆GG(C)₄GCCCA(C)₄GCCTCGCG(GCCCCCGGCCCC)₂	ins(C)₄G(C)₆GG(C)₄GCCCA(C)₄GCCTCGCG(GCCCCCGGCCCC)₂GCCCA(C)₄GCCTCGCG(GCCCCCG)₂(GCCCC)₂(CGGCCCCGCCCCGCCCCC)₂CGG(C)₄G(C)₅GG(C)₄	ins(C)₄G(C)₆GG(C)₄G(C)₅GG(C)₄	ins(C)₄G(C)₅GG(C)₄	ins(CCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGG)₂(C)₄G(C)₅GG(C)₄	ins(CCCCG)₂(C)₆GG(C)₄GCCCA(C)₄GCCTCGCG(GCCCCCGGCCCC)₂	ins(CCCCG)₂(C)₅GG(C)₄	ins(C)₄G(C)₄TCGG(C)₄	ins(C)₄GG(C)₄	ins(C)₄GG(C)₅	ins(CCCCGGC)₂CCCG(C)₅GG(C)₄	ins(C)₄T(C)₄	insT(C)₄GG(C)₄
GRCh38.p14 chr 20	NC_000020.11:g.407965_407966=	NC_000020.11:g.407965_407966insC	NC_000020.11:g.407965_407966insCCC	NC_000020.11:g.407965_407966insCCCACCCC	NC_000020.11:g.407965_407966insCCCACCCCGCCTCGCGGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCC	NC_000020.11:g.407965_407966insCCCCAGGCCCC	NC_000020.11:g.407965_407966insCCCCCCGGGGCC	NC_000020.11:g.407965_407966insCCCCCGCCCCC	NC_000020.11:g.407965_407966insCCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCCGCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCCGGCACC	NC_000020.11:g.407965_407966insCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCCGGCCCCGCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCCGTCCCC	NC_000020.11:g.407965_407966insCCCCGC	NC_000020.11:g.407965_407966insCCCCGCCCC	NC_000020.11:g.407965_407966insCCCCGCCCCCC	NC_000020.11:g.407965_407966insCCCCGCCCCCCGCCCC	NC_000020.11:g.407965_407966insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCC	NC_000020.11:g.407965_407966insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCGCCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCGCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCGCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCGCCCCTCGGCCCC	NC_000020.11:g.407965_407966insCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCGGCCCCC	NC_000020.11:g.407965_407966insCCCCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:g.407965_407966insCCCCTCCCC	NC_000020.11:g.407965_407966insTCCCCGGCCCC
GRCh37.p13 chr 20	NC_000020.10:g.388609_388610=	NC_000020.10:g.388609_388610insC	NC_000020.10:g.388609_388610insCCC	NC_000020.10:g.388609_388610insCCCACCCC	NC_000020.10:g.388609_388610insCCCACCCCGCCTCGCGGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCC	NC_000020.10:g.388609_388610insCCCCAGGCCCC	NC_000020.10:g.388609_388610insCCCCCCGGGGCC	NC_000020.10:g.388609_388610insCCCCCGCCCCC	NC_000020.10:g.388609_388610insCCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCCGCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCCGGCACC	NC_000020.10:g.388609_388610insCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCCGGCCCCGCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCCGTCCCC	NC_000020.10:g.388609_388610insCCCCGC	NC_000020.10:g.388609_388610insCCCCGCCCC	NC_000020.10:g.388609_388610insCCCCGCCCCCC	NC_000020.10:g.388609_388610insCCCCGCCCCCCGCCCC	NC_000020.10:g.388609_388610insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCC	NC_000020.10:g.388609_388610insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCGCCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCGCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCGCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCGCCCCTCGGCCCC	NC_000020.10:g.388609_388610insCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCGGCCCCC	NC_000020.10:g.388609_388610insCCCCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.10:g.388609_388610insCCCCTCCCC	NC_000020.10:g.388609_388610insTCCCCGGCCCC
RBCK1 RefSeqGene (LRG_728)	NG_033233.1:g.4901_4902=	NG_033233.1:g.4901_4902insC	NG_033233.1:g.4901_4902insCCC	NG_033233.1:g.4901_4902insCCCACCCC	NG_033233.1:g.4901_4902insCCCACCCCGCCTCGCGGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCC	NG_033233.1:g.4901_4902insCCCCAGGCCCC	NG_033233.1:g.4901_4902insCCCCCCGGGGCC	NG_033233.1:g.4901_4902insCCCCCGCCCCC	NG_033233.1:g.4901_4902insCCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCCGCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCCGGCACC	NG_033233.1:g.4901_4902insCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCCGGCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCCGGCCCCGCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCCGTCCCC	NG_033233.1:g.4901_4902insCCCCGC	NG_033233.1:g.4901_4902insCCCCGCCCC	NG_033233.1:g.4901_4902insCCCCGCCCCCC	NG_033233.1:g.4901_4902insCCCCGCCCCCCGCCCC	NG_033233.1:g.4901_4902insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCC	NG_033233.1:g.4901_4902insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCGCCCCCCGGCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCGCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCGCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCGCCCCTCGGCCCC	NG_033233.1:g.4901_4902insCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCGGCCCCC	NG_033233.1:g.4901_4902insCCCCGGCCCCCGGCCCCGCCCCCGGCCCC	NG_033233.1:g.4901_4902insCCCCTCCCC	NG_033233.1:g.4901_4902insTCCCCGGCCCC

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#.

40 SubSNP, 36 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3706410927	Jul 13, 2019 (153)
2	EVA_DECODE	ss3706410928	Jul 13, 2019 (153)
3	EVA_DECODE	ss3706410929	Jul 13, 2019 (153)
4	EVA_DECODE	ss3706410930	Jul 13, 2019 (153)
5	GNOMAD	ss4333860399	Apr 26, 2021 (155)
6	GNOMAD	ss4333860400	Apr 26, 2021 (155)
7	GNOMAD	ss4333860401	Apr 26, 2021 (155)
8	GNOMAD	ss4333860402	Apr 26, 2021 (155)
9	GNOMAD	ss4333860403	Apr 26, 2021 (155)
10	GNOMAD	ss4333860404	Apr 26, 2021 (155)
11	GNOMAD	ss4333860405	Apr 26, 2021 (155)
12	GNOMAD	ss4333860406	Apr 26, 2021 (155)
13	GNOMAD	ss4333860407	Apr 26, 2021 (155)
14	GNOMAD	ss4333860408	Apr 26, 2021 (155)
15	GNOMAD	ss4333860409	Apr 26, 2021 (155)
16	GNOMAD	ss4333860410	Apr 26, 2021 (155)
17	GNOMAD	ss4333860411	Apr 26, 2021 (155)
18	GNOMAD	ss4333860412	Apr 26, 2021 (155)
19	GNOMAD	ss4333860413	Apr 26, 2021 (155)
20	GNOMAD	ss4333860414	Apr 26, 2021 (155)
21	GNOMAD	ss4333860415	Apr 26, 2021 (155)
22	GNOMAD	ss4333860416	Apr 26, 2021 (155)
23	GNOMAD	ss4333860417	Apr 26, 2021 (155)
24	GNOMAD	ss4333860418	Apr 26, 2021 (155)
25	GNOMAD	ss4333860419	Apr 26, 2021 (155)
26	GNOMAD	ss4333860420	Apr 26, 2021 (155)
27	GNOMAD	ss4333860421	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5228517544	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5228517545	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5228517547	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5228517548	Apr 26, 2021 (155)
32	1000G_HIGH_COVERAGE	ss5307829886	Oct 13, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5307829888	Oct 13, 2022 (156)
34	HUGCELL_USP	ss5500254388	Oct 13, 2022 (156)
35	HUGCELL_USP	ss5500254389	Oct 13, 2022 (156)
36	HUGCELL_USP	ss5500254390	Oct 13, 2022 (156)
37	TOMMO_GENOMICS	ss5787412785	Oct 13, 2022 (156)
38	TOMMO_GENOMICS	ss5787412786	Oct 13, 2022 (156)
39	TOMMO_GENOMICS	ss5787412787	Oct 13, 2022 (156)
40	TOMMO_GENOMICS	ss5787412788	Oct 13, 2022 (156)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544448353 (NC_000020.11:407965::C 92/38442) Row 544448354 (NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC 1/38468) Row 544448355 (NC_000020.11:407965::CCCCCCGGGGCC 1/38468)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 86486851 (NC_000020.10:388609::CCCCCGGCCCC 892/6512) Row 86486852 (NC_000020.10:388609::C 27/6512) Row 86486854 (NC_000020.10:388609::CCCC 770/6512)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 86486851 (NC_000020.10:388609::CCCCCGGCCCC 892/6512) Row 86486852 (NC_000020.10:388609::C 27/6512) Row 86486854 (NC_000020.10:388609::CCCC 770/6512)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 86486851 (NC_000020.10:388609::CCCCCGGCCCC 892/6512) Row 86486852 (NC_000020.10:388609::C 27/6512) Row 86486854 (NC_000020.10:388609::CCCC 770/6512)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 86486851 (NC_000020.10:388609::CCCCCGGCCCC 892/6512) Row 86486852 (NC_000020.10:388609::C 27/6512) Row 86486854 (NC_000020.10:388609::CCCC 770/6512)...	-	Apr 26, 2021 (155)
72	14KJPN Submission ignored due to conflicting rows: Row 121249889 (NC_000020.11:407965::CCCCCGGCCCC 1210/19174) Row 121249890 (NC_000020.11:407965::C 56/19174) Row 121249891 (NC_000020.11:407965::CCCC 1328/19174)...	-	Oct 13, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 121249889 (NC_000020.11:407965::CCCCCGGCCCC 1210/19174) Row 121249890 (NC_000020.11:407965::C 56/19174) Row 121249891 (NC_000020.11:407965::CCCC 1328/19174)...	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 121249889 (NC_000020.11:407965::CCCCCGGCCCC 1210/19174) Row 121249890 (NC_000020.11:407965::C 56/19174) Row 121249891 (NC_000020.11:407965::CCCC 1328/19174)...	-	Oct 13, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 121249889 (NC_000020.11:407965::CCCCCGGCCCC 1210/19174) Row 121249890 (NC_000020.11:407965::C 56/19174) Row 121249891 (NC_000020.11:407965::CCCC 1328/19174)...	-	Oct 13, 2022 (156)
76	ALFA	NC_000020.11 - 407966	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).

Added to this RefSNP Cluster:

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1491492011

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.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5228517545	NC_000020.10:388609::C	NC_000020.11:407965::C	(self)
1211368606, ss4333860399, ss5500254390, ss5787412786	NC_000020.11:407965::C	NC_000020.11:407965::C	(self)
1211368606	NC_000020.11:407965::CCC	NC_000020.11:407965::CCC	(self)
ss3706410927	NC_000020.11:407965::CCCACCCC	NC_000020.11:407965::CCCACCCC	(self)
ss4333860400	NC_000020.11:407965::CCCACCCCGCCTC… NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC	NC_000020.11:407965::CCCACCCCGCCTC… NC_000020.11:407965::CCCACCCCGCCTCGCGGCCCCCGGCCCC	(self)
ss5228517547	NC_000020.10:388609::CCCC	NC_000020.11:407965::CCCC	(self)
1211368606, ss3706410929, ss5500254389, ss5787412787	NC_000020.11:407965::CCCC	NC_000020.11:407965::CCCC	(self)
1211368606	NC_000020.11:407965::CCCCAGGCCCC	NC_000020.11:407965::CCCCAGGCCCC	(self)
ss4333860401	NC_000020.11:407965::CCCCCCGGGGCC	NC_000020.11:407965::CCCCCCGGGGCC	(self)
1211368606, ss4333860402	NC_000020.11:407965::CCCCCGCCCCC	NC_000020.11:407965::CCCCCGCCCCC	(self)
ss4333860403	NC_000020.11:407965::CCCCCGCCCCCGG… NC_000020.11:407965::CCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCCGCCCCCGG… NC_000020.11:407965::CCCCCGCCCCCGGCCCC	(self)
1211368606	NC_000020.11:407965::CCCCCGCCCCGCC… NC_000020.11:407965::CCCCCGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCCGCCCCGCC… NC_000020.11:407965::CCCCCGCCCCGCCCCCGGCCCC	(self)
1211368606, ss4333860404	NC_000020.11:407965::CCCCCGGCACC	NC_000020.11:407965::CCCCCGGCACC	(self)
ss5228517544	NC_000020.10:388609::CCCCCGGCCCC	NC_000020.11:407965::CCCCCGGCCCC	(self)
1211368606, ss4333860405, ss5307829886, ss5500254388, ss5787412785	NC_000020.11:407965::CCCCCGGCCCC	NC_000020.11:407965::CCCCCGGCCCC	(self)
ss5228517548	NC_000020.10:388609::CCCCCGGCCCCGC… NC_000020.10:388609::CCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCCGGCCCCGC… NC_000020.11:407965::CCCCCGGCCCCGCCCCCGGCCCC	(self)
1211368606, ss3706410928, ss4333860406, ss5307829888, ss5787412788	NC_000020.11:407965::CCCCCGGCCCCGC… NC_000020.11:407965::CCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCCGGCCCCGC… NC_000020.11:407965::CCCCCGGCCCCGCCCCCGGCCCC	(self)
ss4333860407	NC_000020.11:407965::CCCCCGGCCCCGC… NC_000020.11:407965::CCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCCGGCCCCGC… NC_000020.11:407965::CCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC	(self)
ss4333860408	NC_000020.11:407965::CCCCCGGCCCCGC… NC_000020.11:407965::CCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCCGGCCCCGC… NC_000020.11:407965::CCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCCGCCCCCGGCCCC	(self)
ss4333860409	NC_000020.11:407965::CCCCCGGCCCCGC… NC_000020.11:407965::CCCCCGGCCCCGCCCCGGCCCC	NC_000020.11:407965::CCCCCGGCCCCGC… NC_000020.11:407965::CCCCCGGCCCCGCCCCGGCCCC	(self)
1211368606	NC_000020.11:407965::CCCCCGTCCCC	NC_000020.11:407965::CCCCCGTCCCC	(self)
ss3706410930	NC_000020.11:407965::CCCCGC	NC_000020.11:407965::CCCCGC	(self)
ss4333860410	NC_000020.11:407965::CCCCGCCCC	NC_000020.11:407965::CCCCGCCCC	(self)
ss4333860411	NC_000020.11:407965::CCCCGCCCCCC	NC_000020.11:407965::CCCCGCCCCCC	(self)
ss4333860412	NC_000020.11:407965::CCCCGCCCCCCGC… NC_000020.11:407965::CCCCGCCCCCCGCCCC	NC_000020.11:407965::CCCCGCCCCCCGC… NC_000020.11:407965::CCCCGCCCCCCGCCCC	(self)
ss4333860413	NC_000020.11:407965::CCCCGCCCCCCGG… NC_000020.11:407965::CCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCC	NC_000020.11:407965::CCCCGCCCCCCGG… NC_000020.11:407965::CCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCC	(self)
	NC_000020.11:407965::CCCCGCCCCCCGG… NC_000020.11:407965::CCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCGCCCCCCGG… NC_000020.11:407965::CCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	(self)
	NC_000020.11:407965::CCCCGCCCCCCGG… NC_000020.11:407965::CCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCGCCCCCCGG… NC_000020.11:407965::CCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCGCCCCCCGGCCCCGCCCCCGGCCCC	(self)
ss4333860414	NC_000020.11:407965::CCCCGCCCCCCGG… NC_000020.11:407965::CCCCGCCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCGCCCCCCGG… NC_000020.11:407965::CCCCGCCCCCCGGCCCCGCCCCCGGCCCC	(self)
ss4333860415	NC_000020.11:407965::CCCCGCCCCCGGC… NC_000020.11:407965::CCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCGCCCCCGGC… NC_000020.11:407965::CCCCGCCCCCGGCCCC	(self)
	NC_000020.11:407965::CCCCGCCCCCGGC… NC_000020.11:407965::CCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCGCCCCCGGC… NC_000020.11:407965::CCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	(self)
	NC_000020.11:407965::CCCCGCCCCGCCC… NC_000020.11:407965::CCCCGCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCGCCCCGCCC… NC_000020.11:407965::CCCCGCCCCGCCCCCCGGCCCCGCCCACCCCGCCTCGCGGCCCCCGGCCCCGCCCCCGGCCCC	(self)
ss4333860416	NC_000020.11:407965::CCCCGCCCCGCCC… NC_000020.11:407965::CCCCGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCGCCCCGCCC… NC_000020.11:407965::CCCCGCCCCGCCCCCGGCCCC	(self)
ss4333860417	NC_000020.11:407965::CCCCGCCCCTCGG… NC_000020.11:407965::CCCCGCCCCTCGGCCCC	NC_000020.11:407965::CCCCGCCCCTCGG… NC_000020.11:407965::CCCCGCCCCTCGGCCCC	(self)
1211368606, ss4333860418	NC_000020.11:407965::CCCCGGCCCC	NC_000020.11:407965::CCCCGGCCCC	(self)
1211368606	NC_000020.11:407965::CCCCGGCCCCC	NC_000020.11:407965::CCCCGGCCCCC	(self)
ss4333860419	NC_000020.11:407965::CCCCGGCCCCCGG… NC_000020.11:407965::CCCCGGCCCCCGGCCCCGCCCCCGGCCCC	NC_000020.11:407965::CCCCGGCCCCCGG… NC_000020.11:407965::CCCCGGCCCCCGGCCCCGCCCCCGGCCCC	(self)
ss4333860420	NC_000020.11:407965::CCCCTCCCC	NC_000020.11:407965::CCCCTCCCC	(self)
ss4333860421	NC_000020.11:407965::TCCCCGGCCCC	NC_000020.11:407965::TCCCCGGCCCC	(self)

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491492011