Name: rs56371820
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.

rs56371820

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:65004869-65004890 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₂ / del(T)₁₀ / del(T)₉ / de…
del(T)₁₂ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / ins(T)₃₁ / ins(T)₃₇ / ins(T)₃₇G(T)₂₂ / ins(T)₃₉
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.3339 (1717/5142, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ERV3-1 : Non Coding Transcript Variant
ERV3-1-ZNF117 : 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	5142	TTTTTTTTTTTTTTTTTTTTTT=0.4300	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0121, TTTTTTTTTTTTTTTTTTTT=0.2153, TTTTTTTTTTTTTTTTTTTTT=0.3339, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0027, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0010, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0051, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.410408	0.21805	0.371542	32
European	Sub	4568	TTTTTTTTTTTTTTTTTTTTTT=0.3597	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0136, TTTTTTTTTTTTTTTTTTTT=0.2417, TTTTTTTTTTTTTTTTTTTTT=0.3752, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0031, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0011, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0057, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.275527	0.267423	0.45705	5
African	Sub	530	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	28	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	502	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 2	Sub	8	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	34	TTTTTTTTTTTTTTTTTTTTTT=0.82	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.09, TTTTTTTTTTTTTTTTTTTTT=0.09, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.928571	0.071429	0.0	8

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
Allele Frequency Aggregator	Total	Global	5142	(T)₂₂=0.4300	del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0121, delTT=0.2153, delT=0.3339, dupT=0.0000, dupTTT=0.0000, dup(T)₅=0.0010, dup(T)₆=0.0027, dup(T)₇=0.0051
Allele Frequency Aggregator	European	Sub	4568	(T)₂₂=0.3597	del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0136, delTT=0.2417, delT=0.3752, dupT=0.0000, dupTTT=0.0000, dup(T)₅=0.0011, dup(T)₆=0.0031, dup(T)₇=0.0057
Allele Frequency Aggregator	African	Sub	530	(T)₂₂=1.000	del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTTT=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	34	(T)₂₂=0.82	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.09, delT=0.09, dupT=0.00, dupTTT=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Latin American 2	Sub	8	(T)₂₂=1.0	del(T)₁₂=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTTT=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0
Allele Frequency Aggregator	Asian	Sub	2	(T)₂₂=1.0	del(T)₁₂=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTTT=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(T)₂₂=0	del(T)₁₂=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTTT=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₂₂=0	del(T)₁₂=0, del(T)₁₀=0, del(T)₉=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTTT=0, dup(T)₅=0, dup(T)₆=0, dup(T)₇=0

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 7	NC_000007.14:g.65004879_65004890del
GRCh38.p14 chr 7	NC_000007.14:g.65004881_65004890del
GRCh38.p14 chr 7	NC_000007.14:g.65004882_65004890del
GRCh38.p14 chr 7	NC_000007.14:g.65004883_65004890del
GRCh38.p14 chr 7	NC_000007.14:g.65004884_65004890del
GRCh38.p14 chr 7	NC_000007.14:g.65004885_65004890del
GRCh38.p14 chr 7	NC_000007.14:g.65004886_65004890del
GRCh38.p14 chr 7	NC_000007.14:g.65004887_65004890del
GRCh38.p14 chr 7	NC_000007.14:g.65004888_65004890del
GRCh38.p14 chr 7	NC_000007.14:g.65004889_65004890del
GRCh38.p14 chr 7	NC_000007.14:g.65004890del
GRCh38.p14 chr 7	NC_000007.14:g.65004890dup
GRCh38.p14 chr 7	NC_000007.14:g.65004889_65004890dup
GRCh38.p14 chr 7	NC_000007.14:g.65004888_65004890dup
GRCh38.p14 chr 7	NC_000007.14:g.65004887_65004890dup
GRCh38.p14 chr 7	NC_000007.14:g.65004886_65004890dup
GRCh38.p14 chr 7	NC_000007.14:g.65004885_65004890dup
GRCh38.p14 chr 7	NC_000007.14:g.65004884_65004890dup
GRCh38.p14 chr 7	NC_000007.14:g.65004883_65004890dup
GRCh38.p14 chr 7	NC_000007.14:g.65004882_65004890dup
GRCh38.p14 chr 7	NC_000007.14:g.65004881_65004890dup
GRCh38.p14 chr 7	NC_000007.14:g.65004890_65004891insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.65004890_65004891insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.65004869_65004890T[59]GTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 7	NC_000007.14:g.65004890_65004891insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.64465257_64465268del
GRCh37.p13 chr 7	NC_000007.13:g.64465259_64465268del
GRCh37.p13 chr 7	NC_000007.13:g.64465260_64465268del
GRCh37.p13 chr 7	NC_000007.13:g.64465261_64465268del
GRCh37.p13 chr 7	NC_000007.13:g.64465262_64465268del
GRCh37.p13 chr 7	NC_000007.13:g.64465263_64465268del
GRCh37.p13 chr 7	NC_000007.13:g.64465264_64465268del
GRCh37.p13 chr 7	NC_000007.13:g.64465265_64465268del
GRCh37.p13 chr 7	NC_000007.13:g.64465266_64465268del
GRCh37.p13 chr 7	NC_000007.13:g.64465267_64465268del
GRCh37.p13 chr 7	NC_000007.13:g.64465268del
GRCh37.p13 chr 7	NC_000007.13:g.64465268dup
GRCh37.p13 chr 7	NC_000007.13:g.64465267_64465268dup
GRCh37.p13 chr 7	NC_000007.13:g.64465266_64465268dup
GRCh37.p13 chr 7	NC_000007.13:g.64465265_64465268dup
GRCh37.p13 chr 7	NC_000007.13:g.64465264_64465268dup
GRCh37.p13 chr 7	NC_000007.13:g.64465263_64465268dup
GRCh37.p13 chr 7	NC_000007.13:g.64465262_64465268dup
GRCh37.p13 chr 7	NC_000007.13:g.64465261_64465268dup
GRCh37.p13 chr 7	NC_000007.13:g.64465260_64465268dup
GRCh37.p13 chr 7	NC_000007.13:g.64465259_64465268dup
GRCh37.p13 chr 7	NC_000007.13:g.64465268_64465269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.64465268_64465269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.64465247_64465268T[59]GTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 7	NC_000007.13:g.64465268_64465269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: ERV3-1, endogenous retrovirus group 3 member 1, envelope (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ERV3-1 transcript variant 1	NM_001007253.4:c.-389+166… NM_001007253.4:c.-389+1661_-389+1672del	N/A	Intron Variant
ERV3-1 transcript variant 4	NM_001396062.1:c.	N/A	Genic Upstream Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.462_473del	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.464_473del	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.465_473del	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.466_473del	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.467_473del	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.468_473del	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.469_473del	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.470_473del	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.471_473del	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.472_473del	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.473del	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.473dup	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.472_473dup	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.471_473dup	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.470_473dup	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.469_473dup	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.468_473dup	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.467_473dup	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.466_473dup	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.465_473dup	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.464_473dup	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.473_474insA… NR_145414.3:n.473_474insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.473_474insA… NR_145414.3:n.473_474insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.452_473A[22… NR_145414.3:n.452_473A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 2	NR_145414.3:n.473_474insA… NR_145414.3:n.473_474insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	N/A	Non Coding Transcript Variant
ERV3-1 transcript variant 3	NR_145415.2:n.	N/A	Genic Downstream Transcript Variant

Gene: ERV3-1-ZNF117, ERV3-1-ZNF117 readthrough (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ERV3-1-ZNF117 transcript	NM_001348050.2:c.-196+166… NM_001348050.2:c.-196+1661_-196+1672del	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)₂₂=	del(T)₁₂	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	ins(T)₃₁	ins(T)₃₇	ins(T)₃₇G(T)₂₂	ins(T)₃₉
GRCh38.p14 chr 7	NC_000007.14:g.65004869_65004890=	NC_000007.14:g.65004879_65004890del	NC_000007.14:g.65004881_65004890del	NC_000007.14:g.65004882_65004890del	NC_000007.14:g.65004883_65004890del	NC_000007.14:g.65004884_65004890del	NC_000007.14:g.65004885_65004890del	NC_000007.14:g.65004886_65004890del	NC_000007.14:g.65004887_65004890del	NC_000007.14:g.65004888_65004890del	NC_000007.14:g.65004889_65004890del	NC_000007.14:g.65004890del	NC_000007.14:g.65004890dup	NC_000007.14:g.65004889_65004890dup	NC_000007.14:g.65004888_65004890dup	NC_000007.14:g.65004887_65004890dup	NC_000007.14:g.65004886_65004890dup	NC_000007.14:g.65004885_65004890dup	NC_000007.14:g.65004884_65004890dup	NC_000007.14:g.65004883_65004890dup	NC_000007.14:g.65004882_65004890dup	NC_000007.14:g.65004881_65004890dup	NC_000007.14:g.65004890_65004891insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.65004890_65004891insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.65004869_65004890T[59]GTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000007.14:g.65004890_65004891insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.64465247_64465268=	NC_000007.13:g.64465257_64465268del	NC_000007.13:g.64465259_64465268del	NC_000007.13:g.64465260_64465268del	NC_000007.13:g.64465261_64465268del	NC_000007.13:g.64465262_64465268del	NC_000007.13:g.64465263_64465268del	NC_000007.13:g.64465264_64465268del	NC_000007.13:g.64465265_64465268del	NC_000007.13:g.64465266_64465268del	NC_000007.13:g.64465267_64465268del	NC_000007.13:g.64465268del	NC_000007.13:g.64465268dup	NC_000007.13:g.64465267_64465268dup	NC_000007.13:g.64465266_64465268dup	NC_000007.13:g.64465265_64465268dup	NC_000007.13:g.64465264_64465268dup	NC_000007.13:g.64465263_64465268dup	NC_000007.13:g.64465262_64465268dup	NC_000007.13:g.64465261_64465268dup	NC_000007.13:g.64465260_64465268dup	NC_000007.13:g.64465259_64465268dup	NC_000007.13:g.64465268_64465269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.64465268_64465269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.64465247_64465268T[59]GTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000007.13:g.64465268_64465269insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ERV3-1 transcript variant 2	NR_145414.3:n.452_473=	NR_145414.3:n.462_473del	NR_145414.3:n.464_473del	NR_145414.3:n.465_473del	NR_145414.3:n.466_473del	NR_145414.3:n.467_473del	NR_145414.3:n.468_473del	NR_145414.3:n.469_473del	NR_145414.3:n.470_473del	NR_145414.3:n.471_473del	NR_145414.3:n.472_473del	NR_145414.3:n.473del	NR_145414.3:n.473dup	NR_145414.3:n.472_473dup	NR_145414.3:n.471_473dup	NR_145414.3:n.470_473dup	NR_145414.3:n.469_473dup	NR_145414.3:n.468_473dup	NR_145414.3:n.467_473dup	NR_145414.3:n.466_473dup	NR_145414.3:n.465_473dup	NR_145414.3:n.464_473dup	NR_145414.3:n.473_474insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NR_145414.3:n.473_474insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NR_145414.3:n.452_473A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NR_145414.3:n.473_474insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ERV3-1 transcript variant 2	NR_145414.2:n.452_473=	NR_145414.2:n.462_473del	NR_145414.2:n.464_473del	NR_145414.2:n.465_473del	NR_145414.2:n.466_473del	NR_145414.2:n.467_473del	NR_145414.2:n.468_473del	NR_145414.2:n.469_473del	NR_145414.2:n.470_473del	NR_145414.2:n.471_473del	NR_145414.2:n.472_473del	NR_145414.2:n.473del	NR_145414.2:n.473dup	NR_145414.2:n.472_473dup	NR_145414.2:n.471_473dup	NR_145414.2:n.470_473dup	NR_145414.2:n.469_473dup	NR_145414.2:n.468_473dup	NR_145414.2:n.467_473dup	NR_145414.2:n.466_473dup	NR_145414.2:n.465_473dup	NR_145414.2:n.464_473dup	NR_145414.2:n.473_474insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NR_145414.2:n.473_474insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NR_145414.2:n.452_473A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NR_145414.2:n.473_474insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ERV3-1 transcript variant 2	NR_145414.1:n.511_532=	NR_145414.1:n.521_532del	NR_145414.1:n.523_532del	NR_145414.1:n.524_532del	NR_145414.1:n.525_532del	NR_145414.1:n.526_532del	NR_145414.1:n.527_532del	NR_145414.1:n.528_532del	NR_145414.1:n.529_532del	NR_145414.1:n.530_532del	NR_145414.1:n.531_532del	NR_145414.1:n.532del	NR_145414.1:n.532dup	NR_145414.1:n.531_532dup	NR_145414.1:n.530_532dup	NR_145414.1:n.529_532dup	NR_145414.1:n.528_532dup	NR_145414.1:n.527_532dup	NR_145414.1:n.526_532dup	NR_145414.1:n.525_532dup	NR_145414.1:n.524_532dup	NR_145414.1:n.523_532dup	NR_145414.1:n.532_533insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NR_145414.1:n.532_533insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NR_145414.1:n.511_532A[22]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NR_145414.1:n.532_533insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ERV3-1 transcript variant 1	NM_001007253.3:c.-389+1672=	NM_001007253.3:c.-389+1661_-389+1672del	NM_001007253.3:c.-389+1663_-389+1672del	NM_001007253.3:c.-389+1664_-389+1672del	NM_001007253.3:c.-389+1665_-389+1672del	NM_001007253.3:c.-389+1666_-389+1672del	NM_001007253.3:c.-389+1667_-389+1672del	NM_001007253.3:c.-389+1668_-389+1672del	NM_001007253.3:c.-389+1669_-389+1672del	NM_001007253.3:c.-389+1670_-389+1672del	NM_001007253.3:c.-389+1671_-389+1672del	NM_001007253.3:c.-389+1672del	NM_001007253.3:c.-389+1672dup	NM_001007253.3:c.-389+1671_-389+1672dup	NM_001007253.3:c.-389+1670_-389+1672dup	NM_001007253.3:c.-389+1669_-389+1672dup	NM_001007253.3:c.-389+1668_-389+1672dup	NM_001007253.3:c.-389+1667_-389+1672dup	NM_001007253.3:c.-389+1666_-389+1672dup	NM_001007253.3:c.-389+1665_-389+1672dup	NM_001007253.3:c.-389+1664_-389+1672dup	NM_001007253.3:c.-389+1663_-389+1672dup	NM_001007253.3:c.-389+1672_-389+1673insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001007253.3:c.-389+1672_-389+1673insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001007253.3:c.-389+1672_-389+1673insAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001007253.3:c.-389+1672_-389+1673insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ERV3-1 transcript variant 1	NM_001007253.4:c.-389+1672=	NM_001007253.4:c.-389+1661_-389+1672del	NM_001007253.4:c.-389+1663_-389+1672del	NM_001007253.4:c.-389+1664_-389+1672del	NM_001007253.4:c.-389+1665_-389+1672del	NM_001007253.4:c.-389+1666_-389+1672del	NM_001007253.4:c.-389+1667_-389+1672del	NM_001007253.4:c.-389+1668_-389+1672del	NM_001007253.4:c.-389+1669_-389+1672del	NM_001007253.4:c.-389+1670_-389+1672del	NM_001007253.4:c.-389+1671_-389+1672del	NM_001007253.4:c.-389+1672del	NM_001007253.4:c.-389+1672dup	NM_001007253.4:c.-389+1671_-389+1672dup	NM_001007253.4:c.-389+1670_-389+1672dup	NM_001007253.4:c.-389+1669_-389+1672dup	NM_001007253.4:c.-389+1668_-389+1672dup	NM_001007253.4:c.-389+1667_-389+1672dup	NM_001007253.4:c.-389+1666_-389+1672dup	NM_001007253.4:c.-389+1665_-389+1672dup	NM_001007253.4:c.-389+1664_-389+1672dup	NM_001007253.4:c.-389+1663_-389+1672dup	NM_001007253.4:c.-389+1672_-389+1673insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001007253.4:c.-389+1672_-389+1673insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001007253.4:c.-389+1672_-389+1673insAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001007253.4:c.-389+1672_-389+1673insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ERV3-1-ZNF117 transcript	NM_001348050.2:c.-196+1672=	NM_001348050.2:c.-196+1661_-196+1672del	NM_001348050.2:c.-196+1663_-196+1672del	NM_001348050.2:c.-196+1664_-196+1672del	NM_001348050.2:c.-196+1665_-196+1672del	NM_001348050.2:c.-196+1666_-196+1672del	NM_001348050.2:c.-196+1667_-196+1672del	NM_001348050.2:c.-196+1668_-196+1672del	NM_001348050.2:c.-196+1669_-196+1672del	NM_001348050.2:c.-196+1670_-196+1672del	NM_001348050.2:c.-196+1671_-196+1672del	NM_001348050.2:c.-196+1672del	NM_001348050.2:c.-196+1672dup	NM_001348050.2:c.-196+1671_-196+1672dup	NM_001348050.2:c.-196+1670_-196+1672dup	NM_001348050.2:c.-196+1669_-196+1672dup	NM_001348050.2:c.-196+1668_-196+1672dup	NM_001348050.2:c.-196+1667_-196+1672dup	NM_001348050.2:c.-196+1666_-196+1672dup	NM_001348050.2:c.-196+1665_-196+1672dup	NM_001348050.2:c.-196+1664_-196+1672dup	NM_001348050.2:c.-196+1663_-196+1672dup	NM_001348050.2:c.-196+1672_-196+1673insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001348050.2:c.-196+1672_-196+1673insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001348050.2:c.-196+1672_-196+1673insAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001348050.2:c.-196+1672_-196+1673insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

62 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77879087	Dec 07, 2007 (129)
2	HUMANGENOME_JCVI	ss95462630	Feb 13, 2009 (130)
3	HUMANGENOME_JCVI	ss98208434	Mar 15, 2016 (147)
4	PJP	ss295338796	May 09, 2011 (134)
5	EVA_UK10K_ALSPAC	ss1705655153	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1705655212	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1710325012	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710332137	Apr 01, 2015 (144)
9	SWEGEN	ss3001300261	Nov 08, 2017 (151)
10	EVA_DECODE	ss3719835282	Jul 13, 2019 (153)
11	EVA_DECODE	ss3719835283	Jul 13, 2019 (153)
12	EVA_DECODE	ss3719835284	Jul 13, 2019 (153)
13	EVA_DECODE	ss3719835285	Jul 13, 2019 (153)
14	ACPOP	ss3734692309	Jul 13, 2019 (153)
15	ACPOP	ss3734692310	Jul 13, 2019 (153)
16	ACPOP	ss3734692311	Jul 13, 2019 (153)
17	ACPOP	ss3734692312	Jul 13, 2019 (153)
18	PACBIO	ss3791139978	Jul 13, 2019 (153)
19	PACBIO	ss3796019831	Jul 13, 2019 (153)
20	EVA	ss3830607029	Apr 26, 2020 (154)
21	GNOMAD	ss4164827603	Apr 26, 2021 (155)
22	GNOMAD	ss4164827604	Apr 26, 2021 (155)
23	GNOMAD	ss4164827605	Apr 26, 2021 (155)
24	GNOMAD	ss4164827606	Apr 26, 2021 (155)
25	GNOMAD	ss4164827607	Apr 26, 2021 (155)
26	GNOMAD	ss4164827608	Apr 26, 2021 (155)
27	GNOMAD	ss4164827609	Apr 26, 2021 (155)
28	GNOMAD	ss4164827610	Apr 26, 2021 (155)
29	GNOMAD	ss4164827611	Apr 26, 2021 (155)
30	GNOMAD	ss4164827612	Apr 26, 2021 (155)
31	GNOMAD	ss4164827613	Apr 26, 2021 (155)
32	GNOMAD	ss4164827614	Apr 26, 2021 (155)
33	GNOMAD	ss4164827615	Apr 26, 2021 (155)
34	GNOMAD	ss4164827616	Apr 26, 2021 (155)
35	GNOMAD	ss4164827617	Apr 26, 2021 (155)
36	GNOMAD	ss4164827618	Apr 26, 2021 (155)
37	GNOMAD	ss4164827619	Apr 26, 2021 (155)
38	GNOMAD	ss4164827620	Apr 26, 2021 (155)
39	GNOMAD	ss4164827621	Apr 26, 2021 (155)
40	GNOMAD	ss4164827622	Apr 26, 2021 (155)
41	GNOMAD	ss4164827623	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5183516934	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5183516935	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5183516936	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5183516937	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5183516938	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5183516939	Apr 26, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5273177167	Oct 14, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5273177168	Oct 14, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5273177169	Oct 14, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5273177170	Oct 14, 2022 (156)
52	HUGCELL_USP	ss5470263357	Oct 14, 2022 (156)
53	HUGCELL_USP	ss5470263358	Oct 14, 2022 (156)
54	HUGCELL_USP	ss5470263359	Oct 14, 2022 (156)
55	HUGCELL_USP	ss5470263360	Oct 14, 2022 (156)
56	TOMMO_GENOMICS	ss5723877022	Oct 14, 2022 (156)
57	TOMMO_GENOMICS	ss5723877023	Oct 14, 2022 (156)
58	TOMMO_GENOMICS	ss5723877024	Oct 14, 2022 (156)
59	TOMMO_GENOMICS	ss5723877025	Oct 14, 2022 (156)
60	TOMMO_GENOMICS	ss5723877026	Oct 14, 2022 (156)
61	EVA	ss5822928456	Oct 14, 2022 (156)
62	EVA	ss5822928457	Oct 14, 2022 (156)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 20818742 (NC_000007.13:64465246:TTT: 1290/3854) Row 20818743 (NC_000007.13:64465247:T: 2508/3854)	-	Oct 12, 2018 (152)
64	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 20818742 (NC_000007.13:64465246:TTT: 1290/3854) Row 20818743 (NC_000007.13:64465247:T: 2508/3854)	-	Oct 12, 2018 (152)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 263574446 (NC_000007.14:65004868::T 253/98904) Row 263574447 (NC_000007.14:65004868::TT 5/98924) Row 263574448 (NC_000007.14:65004868::TTT 2/98926)...	-	Apr 26, 2021 (155)
87	Northern Sweden Submission ignored due to conflicting rows: Row 7977174 (NC_000007.13:64465246:TT: 90/586) Row 7977175 (NC_000007.13:64465246::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 2/586) Row 7977176 (NC_000007.13:64465246:TTT: 12/586)...	-	Jul 13, 2019 (153)
88	Northern Sweden Submission ignored due to conflicting rows: Row 7977174 (NC_000007.13:64465246:TT: 90/586) Row 7977175 (NC_000007.13:64465246::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 2/586) Row 7977176 (NC_000007.13:64465246:TTT: 12/586)...	-	Jul 13, 2019 (153)
89	Northern Sweden Submission ignored due to conflicting rows: Row 7977174 (NC_000007.13:64465246:TT: 90/586) Row 7977175 (NC_000007.13:64465246::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 2/586) Row 7977176 (NC_000007.13:64465246:TTT: 12/586)...	-	Jul 13, 2019 (153)
90	Northern Sweden Submission ignored due to conflicting rows: Row 7977174 (NC_000007.13:64465246:TT: 90/586) Row 7977175 (NC_000007.13:64465246::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 2/586) Row 7977176 (NC_000007.13:64465246:TTT: 12/586)...	-	Jul 13, 2019 (153)
91	8.3KJPN Submission ignored due to conflicting rows: Row 41486241 (NC_000007.13:64465246:T: 7283/16694) Row 41486242 (NC_000007.13:64465246:TT: 5722/16694) Row 41486243 (NC_000007.13:64465246:TTT: 241/16694)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 41486241 (NC_000007.13:64465246:T: 7283/16694) Row 41486242 (NC_000007.13:64465246:TT: 5722/16694) Row 41486243 (NC_000007.13:64465246:TTT: 241/16694)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 41486241 (NC_000007.13:64465246:T: 7283/16694) Row 41486242 (NC_000007.13:64465246:TT: 5722/16694) Row 41486243 (NC_000007.13:64465246:TTT: 241/16694)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 41486241 (NC_000007.13:64465246:T: 7283/16694) Row 41486242 (NC_000007.13:64465246:TT: 5722/16694) Row 41486243 (NC_000007.13:64465246:TTT: 241/16694)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 41486241 (NC_000007.13:64465246:T: 7283/16694) Row 41486242 (NC_000007.13:64465246:TT: 5722/16694) Row 41486243 (NC_000007.13:64465246:TTT: 241/16694)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 41486241 (NC_000007.13:64465246:T: 7283/16694) Row 41486242 (NC_000007.13:64465246:TT: 5722/16694) Row 41486243 (NC_000007.13:64465246:TTT: 241/16694)...	-	Apr 26, 2021 (155)
97	14KJPN Submission ignored due to conflicting rows: Row 57714126 (NC_000007.14:65004868:T: 12888/28050) Row 57714127 (NC_000007.14:65004868:TT: 9743/28050) Row 57714128 (NC_000007.14:65004868:TTT: 413/28050)...	-	Oct 14, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 57714126 (NC_000007.14:65004868:T: 12888/28050) Row 57714127 (NC_000007.14:65004868:TT: 9743/28050) Row 57714128 (NC_000007.14:65004868:TTT: 413/28050)...	-	Oct 14, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 57714126 (NC_000007.14:65004868:T: 12888/28050) Row 57714127 (NC_000007.14:65004868:TT: 9743/28050) Row 57714128 (NC_000007.14:65004868:TTT: 413/28050)...	-	Oct 14, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 57714126 (NC_000007.14:65004868:T: 12888/28050) Row 57714127 (NC_000007.14:65004868:TT: 9743/28050) Row 57714128 (NC_000007.14:65004868:TTT: 413/28050)...	-	Oct 14, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 57714126 (NC_000007.14:65004868:T: 12888/28050) Row 57714127 (NC_000007.14:65004868:TT: 9743/28050) Row 57714128 (NC_000007.14:65004868:TTT: 413/28050)...	-	Oct 14, 2022 (156)
102	UK 10K study - Twins Submission ignored due to conflicting rows: Row 20818742 (NC_000007.13:64465246:TTT: 1211/3708) Row 20818743 (NC_000007.13:64465247:T: 2446/3708)	-	Oct 12, 2018 (152)
103	UK 10K study - Twins Submission ignored due to conflicting rows: Row 20818742 (NC_000007.13:64465246:TTT: 1211/3708) Row 20818743 (NC_000007.13:64465247:T: 2446/3708)	-	Oct 12, 2018 (152)
104	ALFA	NC_000007.14 - 65004869	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
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4164827623	NC_000007.14:65004868:TTTTTTTTT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4164827622	NC_000007.14:65004868:TTTTTTTT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4164827621	NC_000007.14:65004868:TTTTTTT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4164827620	NC_000007.14:65004868:TTTTTT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4164827619	NC_000007.14:65004868:TTTTT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4164827618	NC_000007.14:65004868:TTTT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss1705655153, ss1705655212, ss3001300261, ss3734692311, ss5183516936, ss5822928457	NC_000007.13:64465246:TTT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3719835282, ss4164827617, ss5273177170, ss5470263360, ss5723877024	NC_000007.14:65004868:TTT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3734692309, ss3830607029, ss5183516935, ss5822928456	NC_000007.13:64465246:TT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss1710325012, ss1710332137	NC_000007.13:64465247:TT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4164827616, ss5273177168, ss5470263357, ss5723877023	NC_000007.14:65004868:TT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3719835283	NC_000007.14:65004869:TT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss98208434	NT_007933.15:2498089:TT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss95462630	NT_007933.15:2498109:TT:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss77879087	NC_000007.11:63909417:T:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss295338796	NC_000007.12:64102702:T:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3734692312, ss3791139978, ss3796019831, ss5183516934	NC_000007.13:64465246:T:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000007.13:64465247:T:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827615, ss5273177167, ss5470263358, ss5723877022	NC_000007.14:65004868:T:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3719835284	NC_000007.14:65004870:T:	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss98208434	NT_007933.15:2498089:TT:T	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5183516937	NC_000007.13:64465246::T	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827603, ss5273177169, ss5470263359, ss5723877025	NC_000007.14:65004868::T	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3719835285	NC_000007.14:65004871::T	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827604	NC_000007.14:65004868::TT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827605	NC_000007.14:65004868::TTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827606	NC_000007.14:65004868::TTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827607	NC_000007.14:65004868::TTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5183516939	NC_000007.13:64465246::TTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827608, ss5723877026	NC_000007.14:65004868::TTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827609	NC_000007.14:65004868::TTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13140010830	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5183516938	NC_000007.13:64465246::TTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827610	NC_000007.14:65004868::TTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827611	NC_000007.14:65004868::TTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827612	NC_000007.14:65004868::TTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827613	NC_000007.14:65004868::TTTTTTTTTTT… NC_000007.14:65004868::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3734692310	NC_000007.13:64465246::TTTTTTTTTTT… NC_000007.13:64465246::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000007.14:65004868::TTTTTTTTTTT… NC_000007.14:65004868::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4164827614	NC_000007.14:65004868::TTTTTTTTTTT… NC_000007.14:65004868::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:65004868:TTTTTTTTTTTT… NC_000007.14:65004868:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs56371820

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs56371820