Name: rs60310859
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.

rs60310859

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr21:27739904-27739919 (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)₆ / del(T)₅ / del(T)₄ / delT…
del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / insTTTG(T)₁₆ / dup(T)₄ / ins(T)₄C(T)₁₉ / dup(T)₆ / dup(T)₇ / ins(T)₇C(T)₁₉ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₆ / ins(T)₁₇ / ins(T)₁₇C(T)₁₉ / ins(T)₁₈ / ins(T)₁₉ / ins(T)₂₀ / ins(T)₂₁ / ins(T)₂₂
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₆=0.000004 (1/264690, TOPMED)
dupT=0.04593 (537/11692, ALFA)
delT=0.1703 (853/5008, 1000G) (+ 1 more)
dupT=0.40 (16/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC00113 : 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	11692	TTTTTTTTTTTTTTTT=0.94663	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00445, TTTTTTTTTTTTTTTTT=0.04593, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00128, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00077, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00051, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00043, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000	0.918966	0.010758	0.070276	32
European	Sub	9530	TTTTTTTTTTTTTTTT=0.9347	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0055, TTTTTTTTTTTTTTTTT=0.0561, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0016, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0006, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	0.900683	0.013242	0.086074	32
African	Sub	1082	TTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	36	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1046	TTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	78	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	62	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	106	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	506	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	82	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	308	TTTTTTTTTTTTTTTT=0.994	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.006, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	0.987013	0.0	0.012987	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)₁₆=0.999996	del(T)₆=0.000004
Allele Frequency Aggregator	Total	Global	11692	(T)₁₆=0.94663	del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00445, dupT=0.04593, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₁₂=0.00077, dup(T)₁₃=0.00128, dup(T)₁₄=0.00051, ins(T)₁₉=0.00043
Allele Frequency Aggregator	European	Sub	9530	(T)₁₆=0.9347	del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0055, dupT=0.0561, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₁₂=0.0009, dup(T)₁₃=0.0016, dup(T)₁₄=0.0006, ins(T)₁₉=0.0005
Allele Frequency Aggregator	African	Sub	1082	(T)₁₆=1.0000	del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₁₂=0.0000, dup(T)₁₃=0.0000, dup(T)₁₄=0.0000, ins(T)₁₉=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	506	(T)₁₆=1.000	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)₁₂=0.000, dup(T)₁₃=0.000, dup(T)₁₄=0.000, ins(T)₁₉=0.000
Allele Frequency Aggregator	Other	Sub	308	(T)₁₆=0.994	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=0.006, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₁₂=0.000, dup(T)₁₃=0.000, dup(T)₁₄=0.000, ins(T)₁₉=0.000
Allele Frequency Aggregator	Latin American 1	Sub	106	(T)₁₆=1.000	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)₁₂=0.000, dup(T)₁₃=0.000, dup(T)₁₄=0.000, ins(T)₁₉=0.000
Allele Frequency Aggregator	South Asian	Sub	82	(T)₁₆=1.00	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)₁₂=0.00, dup(T)₁₃=0.00, dup(T)₁₄=0.00, ins(T)₁₉=0.00
Allele Frequency Aggregator	Asian	Sub	78	(T)₁₆=1.00	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)₁₂=0.00, dup(T)₁₃=0.00, dup(T)₁₄=0.00, ins(T)₁₉=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₆=0.8297	delT=0.1703
1000Genomes	African	Sub	1322	(T)₁₆=0.6241	delT=0.3759
1000Genomes	East Asian	Sub	1008	(T)₁₆=0.9335	delT=0.0665
1000Genomes	Europe	Sub	1006	(T)₁₆=0.8529	delT=0.1471
1000Genomes	South Asian	Sub	978	(T)₁₆=0.952	delT=0.048
1000Genomes	American	Sub	694	(T)₁₆=0.865	delT=0.135
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.40

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 21	NC_000021.9:g.27739914_27739919del
GRCh38.p14 chr 21	NC_000021.9:g.27739915_27739919del
GRCh38.p14 chr 21	NC_000021.9:g.27739916_27739919del
GRCh38.p14 chr 21	NC_000021.9:g.27739917_27739919del
GRCh38.p14 chr 21	NC_000021.9:g.27739918_27739919del
GRCh38.p14 chr 21	NC_000021.9:g.27739919del
GRCh38.p14 chr 21	NC_000021.9:g.27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739918_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739917_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739904_27739919T[19]GTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 21	NC_000021.9:g.27739916_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739904_27739919T[20]CTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 21	NC_000021.9:g.27739914_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739913_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739904_27739919T[23]CTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 21	NC_000021.9:g.27739911_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739910_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739909_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739908_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739907_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739906_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739905_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739904_27739919dup
GRCh38.p14 chr 21	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 21	NC_000021.9:g.27739904_27739919T[33]CTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 21	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 21	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 21	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 21	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 21	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 21	NC_000021.8:g.29112233_29112238del
GRCh37.p13 chr 21	NC_000021.8:g.29112234_29112238del
GRCh37.p13 chr 21	NC_000021.8:g.29112235_29112238del
GRCh37.p13 chr 21	NC_000021.8:g.29112236_29112238del
GRCh37.p13 chr 21	NC_000021.8:g.29112237_29112238del
GRCh37.p13 chr 21	NC_000021.8:g.29112238del
GRCh37.p13 chr 21	NC_000021.8:g.29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112237_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112236_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112223_29112238T[19]GTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 21	NC_000021.8:g.29112235_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112223_29112238T[20]CTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 21	NC_000021.8:g.29112233_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112232_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112223_29112238T[23]CTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 21	NC_000021.8:g.29112230_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112229_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112228_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112227_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112226_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112225_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112224_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112223_29112238dup
GRCh37.p13 chr 21	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 21	NC_000021.8:g.29112223_29112238T[33]CTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 21	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 21	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 21	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 21	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 21	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTTTTTTT

Gene: LINC00113, long intergenic non-protein coding RNA 113 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC00113 transcript	NR_024357.2: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)₁₆=	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	insTTTG(T)₁₆	dup(T)₄	ins(T)₄C(T)₁₉	dup(T)₆	dup(T)₇	ins(T)₇C(T)₁₉	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	dup(T)₁₆	ins(T)₁₇	ins(T)₁₇C(T)₁₉	ins(T)₁₈	ins(T)₁₉	ins(T)₂₀	ins(T)₂₁	ins(T)₂₂
GRCh38.p14 chr 21	NC_000021.9:g.27739904_27739919=	NC_000021.9:g.27739914_27739919del	NC_000021.9:g.27739915_27739919del	NC_000021.9:g.27739916_27739919del	NC_000021.9:g.27739917_27739919del	NC_000021.9:g.27739918_27739919del	NC_000021.9:g.27739919del	NC_000021.9:g.27739919dup	NC_000021.9:g.27739918_27739919dup	NC_000021.9:g.27739917_27739919dup	NC_000021.9:g.27739904_27739919T[19]GTTTTTTTTTTTTTTTT[1]	NC_000021.9:g.27739916_27739919dup	NC_000021.9:g.27739904_27739919T[20]CTTTTTTTTTTTTTTTTTTT[1]	NC_000021.9:g.27739914_27739919dup	NC_000021.9:g.27739913_27739919dup	NC_000021.9:g.27739904_27739919T[23]CTTTTTTTTTTTTTTTTTTT[1]	NC_000021.9:g.27739911_27739919dup	NC_000021.9:g.27739910_27739919dup	NC_000021.9:g.27739909_27739919dup	NC_000021.9:g.27739908_27739919dup	NC_000021.9:g.27739907_27739919dup	NC_000021.9:g.27739906_27739919dup	NC_000021.9:g.27739905_27739919dup	NC_000021.9:g.27739904_27739919dup	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTT	NC_000021.9:g.27739904_27739919T[33]CTTTTTTTTTTTTTTTTTTT[1]	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTTT	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTTTT	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTTTTT	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:g.27739919_27739920insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 21	NC_000021.8:g.29112223_29112238=	NC_000021.8:g.29112233_29112238del	NC_000021.8:g.29112234_29112238del	NC_000021.8:g.29112235_29112238del	NC_000021.8:g.29112236_29112238del	NC_000021.8:g.29112237_29112238del	NC_000021.8:g.29112238del	NC_000021.8:g.29112238dup	NC_000021.8:g.29112237_29112238dup	NC_000021.8:g.29112236_29112238dup	NC_000021.8:g.29112223_29112238T[19]GTTTTTTTTTTTTTTTT[1]	NC_000021.8:g.29112235_29112238dup	NC_000021.8:g.29112223_29112238T[20]CTTTTTTTTTTTTTTTTTTT[1]	NC_000021.8:g.29112233_29112238dup	NC_000021.8:g.29112232_29112238dup	NC_000021.8:g.29112223_29112238T[23]CTTTTTTTTTTTTTTTTTTT[1]	NC_000021.8:g.29112230_29112238dup	NC_000021.8:g.29112229_29112238dup	NC_000021.8:g.29112228_29112238dup	NC_000021.8:g.29112227_29112238dup	NC_000021.8:g.29112226_29112238dup	NC_000021.8:g.29112225_29112238dup	NC_000021.8:g.29112224_29112238dup	NC_000021.8:g.29112223_29112238dup	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTT	NC_000021.8:g.29112223_29112238T[33]CTTTTTTTTTTTTTTTTTTT[1]	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTTT	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTTTT	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTTTTT	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTTTTTT	NC_000021.8:g.29112238_29112239insTTTTTTTTTTTTTTTTTTTTTT

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#.

61 SubSNP, 40 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss83306898	Dec 15, 2007 (129)
2	BILGI_BIOE	ss666759885	Apr 25, 2013 (138)
3	1000GENOMES	ss1378721398	Aug 21, 2014 (142)
4	EVA_GENOME_DK	ss1575768315	Apr 01, 2015 (144)
5	SWEGEN	ss3018775062	Nov 08, 2017 (151)
6	MCHAISSO	ss3065837658	Jan 10, 2018 (151)
7	EVA_DECODE	ss3707586739	Jul 13, 2019 (153)
8	EVA_DECODE	ss3707586740	Jul 13, 2019 (153)
9	EVA_DECODE	ss3707586741	Jul 13, 2019 (153)
10	EVA_DECODE	ss3707586742	Jul 13, 2019 (153)
11	PACBIO	ss3793618192	Jul 13, 2019 (153)
12	PACBIO	ss3793618193	Jul 13, 2019 (153)
13	PACBIO	ss3798504338	Jul 13, 2019 (153)
14	PACBIO	ss3798504339	Jul 13, 2019 (153)
15	KHV_HUMAN_GENOMES	ss3822184143	Jul 13, 2019 (153)
16	EVA	ss3835834595	Apr 27, 2020 (154)
17	GNOMAD	ss4359114625	Apr 26, 2021 (155)
18	GNOMAD	ss4359114626	Apr 26, 2021 (155)
19	GNOMAD	ss4359114627	Apr 26, 2021 (155)
20	GNOMAD	ss4359114628	Apr 26, 2021 (155)
21	GNOMAD	ss4359114629	Apr 26, 2021 (155)
22	GNOMAD	ss4359114630	Apr 26, 2021 (155)
23	GNOMAD	ss4359114631	Apr 26, 2021 (155)
24	GNOMAD	ss4359114632	Apr 26, 2021 (155)
25	GNOMAD	ss4359114633	Apr 26, 2021 (155)
26	GNOMAD	ss4359114634	Apr 26, 2021 (155)
27	GNOMAD	ss4359114635	Apr 26, 2021 (155)
28	GNOMAD	ss4359114636	Apr 26, 2021 (155)
29	GNOMAD	ss4359114637	Apr 26, 2021 (155)
30	GNOMAD	ss4359114638	Apr 26, 2021 (155)
31	GNOMAD	ss4359114639	Apr 26, 2021 (155)
32	GNOMAD	ss4359114640	Apr 26, 2021 (155)
33	GNOMAD	ss4359114641	Apr 26, 2021 (155)
34	GNOMAD	ss4359114642	Apr 26, 2021 (155)
35	GNOMAD	ss4359114643	Apr 26, 2021 (155)
36	GNOMAD	ss4359114644	Apr 26, 2021 (155)
37	GNOMAD	ss4359114645	Apr 26, 2021 (155)
38	GNOMAD	ss4359114646	Apr 26, 2021 (155)
39	GNOMAD	ss4359114647	Apr 26, 2021 (155)
40	GNOMAD	ss4359114648	Apr 26, 2021 (155)
41	GNOMAD	ss4359114650	Apr 26, 2021 (155)
42	GNOMAD	ss4359114651	Apr 26, 2021 (155)
43	GNOMAD	ss4359114652	Apr 26, 2021 (155)
44	GNOMAD	ss4359114653	Apr 26, 2021 (155)
45	TOPMED	ss5099152404	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5231209028	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5231209029	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5231209030	Apr 26, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5309965717	Oct 13, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5309965718	Oct 13, 2022 (156)
51	HUGCELL_USP	ss5502036334	Oct 13, 2022 (156)
52	HUGCELL_USP	ss5502036335	Oct 13, 2022 (156)
53	HUGCELL_USP	ss5502036336	Oct 13, 2022 (156)
54	HUGCELL_USP	ss5502036337	Oct 13, 2022 (156)
55	TOMMO_GENOMICS	ss5791631559	Oct 13, 2022 (156)
56	TOMMO_GENOMICS	ss5791631560	Oct 13, 2022 (156)
57	TOMMO_GENOMICS	ss5791631561	Oct 13, 2022 (156)
58	TOMMO_GENOMICS	ss5791631563	Oct 13, 2022 (156)
59	TOMMO_GENOMICS	ss5791631564	Oct 13, 2022 (156)
60	YY_MCH	ss5818383001	Oct 13, 2022 (156)
61	EVA	ss5853272755	Oct 13, 2022 (156)
62	1000Genomes	NC_000021.8 - 29112223	Oct 12, 2018 (152)
63	The Danish reference pan genome	NC_000021.8 - 29112223	Apr 27, 2020 (154)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 561176385 (NC_000021.9:27739903::T 17256/118886) Row 561176386 (NC_000021.9:27739903::TT 589/118932) Row 561176387 (NC_000021.9:27739903::TTT 51/118882)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 89178335 (NC_000021.8:29112222::T 1224/16738) Row 89178336 (NC_000021.8:29112222:T: 57/16738) Row 89178337 (NC_000021.8:29112222::TT 7/16738)	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 89178335 (NC_000021.8:29112222::T 1224/16738) Row 89178336 (NC_000021.8:29112222:T: 57/16738) Row 89178337 (NC_000021.8:29112222::TT 7/16738)	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 89178335 (NC_000021.8:29112222::T 1224/16738) Row 89178336 (NC_000021.8:29112222:T: 57/16738) Row 89178337 (NC_000021.8:29112222::TT 7/16738)	-	Apr 26, 2021 (155)
95	14KJPN Submission ignored due to conflicting rows: Row 125468663 (NC_000021.9:27739903::T 1998/28204) Row 125468664 (NC_000021.9:27739903:T: 108/28204) Row 125468665 (NC_000021.9:27739903::TTT 19/28204)...	-	Oct 13, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 125468663 (NC_000021.9:27739903::T 1998/28204) Row 125468664 (NC_000021.9:27739903:T: 108/28204) Row 125468665 (NC_000021.9:27739903::TTT 19/28204)...	-	Oct 13, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 125468663 (NC_000021.9:27739903::T 1998/28204) Row 125468664 (NC_000021.9:27739903:T: 108/28204) Row 125468665 (NC_000021.9:27739903::TTT 19/28204)...	-	Oct 13, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 125468663 (NC_000021.9:27739903::T 1998/28204) Row 125468664 (NC_000021.9:27739903:T: 108/28204) Row 125468665 (NC_000021.9:27739903::TTT 19/28204)...	-	Oct 13, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 125468663 (NC_000021.9:27739903::T 1998/28204) Row 125468664 (NC_000021.9:27739903:T: 108/28204) Row 125468665 (NC_000021.9:27739903::TTT 19/28204)...	-	Oct 13, 2022 (156)
100	TopMed	NC_000021.9 - 27739904	Apr 26, 2021 (155)
101	ALFA	NC_000021.9 - 27739904	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:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
374261350, ss4359114653, ss5099152404	NC_000021.9:27739903:TTTTTT:	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4359114652	NC_000021.9:27739903:TTT:	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3065837658, ss4359114651	NC_000021.9:27739903:TT:	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss83306898	NC_000021.7:28034108:T:	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
79505906, ss1378721398, ss3018775062, ss3793618192, ss3798504338, ss5231209029	NC_000021.8:29112222:T:	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3707586739, ss3822184143, ss4359114650, ss5309965717, ss5502036334, ss5791631560	NC_000021.9:27739903:T:	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
777496, ss666759885, ss1575768315, ss3793618193, ss3798504339, ss3835834595, ss5231209028	NC_000021.8:29112222::T	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4359114625, ss5309965718, ss5502036335, ss5791631559, ss5818383001, ss5853272755	NC_000021.9:27739903::T	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3707586740	NC_000021.9:27739904::T	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5231209030	NC_000021.8:29112222::TT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4359114626, ss5502036336, ss5791631563	NC_000021.9:27739903::TT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3707586741	NC_000021.9:27739904::TT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4359114627, ss5791631561	NC_000021.9:27739903::TTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3707586742	NC_000021.9:27739904::TTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4359114642	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTTTTTTG	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTT	(self)
ss4359114628	NC_000021.9:27739903::TTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4359114644	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTTTTTTTCTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss4359114629, ss5502036337	NC_000021.9:27739903::TTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114630	NC_000021.9:27739903::TTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114647	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTTTTTTTTTTCTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss4359114631	NC_000021.9:27739903::TTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114632	NC_000021.9:27739903::TTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114633	NC_000021.9:27739903::TTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114634	NC_000021.9:27739903::TTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114635	NC_000021.9:27739903::TTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114636	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114637	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114638	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114639	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114648	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss4359114640	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114641	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11355521080	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114643, ss5791631564	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114645	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4359114646	NC_000021.9:27739903::TTTTTTTTTTTT… NC_000021.9:27739903::TTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:27739903:TTTTTTTTTTTTT… NC_000021.9:27739903:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs60310859

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

rs60310859