Name: rs869189901
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.

rs869189901

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:139577405-139577429 (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)₁₄ / del(T)₁₃ / del(T)₁₂ / d…
del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / 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)₁₁ / ins(T)₂₉
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.02095 (285/13604, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: UBE2D2 : 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	13604	TTTTTTTTTTTTTTTTTTTTTTTTT=0.93575	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.01720, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.02095, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.01999, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00228, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00176, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00206	0.969649	0.007508	0.022843	32
European	Sub	11000	TTTTTTTTTTTTTTTTTTTTTTTTT=0.92055	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.02127, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.02591, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.02473, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00282, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00218, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00255	0.961678	0.00948	0.028842	32
African	Sub	1798	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	72	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1726	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	76	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	60	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	82	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	312	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	32	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	304	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	13604	(T)₂₅=0.93575	del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.01720, dupT=0.02095, dupTT=0.01999, dupTTT=0.00228, dup(T)₄=0.00176, dup(T)₇=0.00206
Allele Frequency Aggregator	European	Sub	11000	(T)₂₅=0.92055	del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.02127, dupT=0.02591, dupTT=0.02473, dupTTT=0.00282, dup(T)₄=0.00218, dup(T)₇=0.00255
Allele Frequency Aggregator	African	Sub	1798	(T)₂₅=1.0000	del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=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)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)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	312	(T)₂₅=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=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)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)₇=0.000
Allele Frequency Aggregator	Other	Sub	304	(T)₂₅=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=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)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)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	82	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=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)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)₇=0.00
Allele Frequency Aggregator	Asian	Sub	76	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=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)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)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	32	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=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)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)₇=0.00

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 5	NC_000005.10:g.139577416_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577417_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577418_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577419_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577420_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577421_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577422_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577423_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577424_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577425_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577426_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577427_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577428_139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577429del
GRCh38.p14 chr 5	NC_000005.10:g.139577429dup
GRCh38.p14 chr 5	NC_000005.10:g.139577428_139577429dup
GRCh38.p14 chr 5	NC_000005.10:g.139577427_139577429dup
GRCh38.p14 chr 5	NC_000005.10:g.139577426_139577429dup
GRCh38.p14 chr 5	NC_000005.10:g.139577425_139577429dup
GRCh38.p14 chr 5	NC_000005.10:g.139577424_139577429dup
GRCh38.p14 chr 5	NC_000005.10:g.139577423_139577429dup
GRCh38.p14 chr 5	NC_000005.10:g.139577422_139577429dup
GRCh38.p14 chr 5	NC_000005.10:g.139577419_139577429dup
GRCh38.p14 chr 5	NC_000005.10:g.139577429_139577430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 5	NC_000005.9:g.138957001_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957002_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957003_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957004_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957005_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957006_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957007_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957008_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957009_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957010_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957011_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957012_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957013_138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957014del
GRCh37.p13 chr 5	NC_000005.9:g.138957014dup
GRCh37.p13 chr 5	NC_000005.9:g.138957013_138957014dup
GRCh37.p13 chr 5	NC_000005.9:g.138957012_138957014dup
GRCh37.p13 chr 5	NC_000005.9:g.138957011_138957014dup
GRCh37.p13 chr 5	NC_000005.9:g.138957010_138957014dup
GRCh37.p13 chr 5	NC_000005.9:g.138957009_138957014dup
GRCh37.p13 chr 5	NC_000005.9:g.138957008_138957014dup
GRCh37.p13 chr 5	NC_000005.9:g.138957007_138957014dup
GRCh37.p13 chr 5	NC_000005.9:g.138957004_138957014dup
GRCh37.p13 chr 5	NC_000005.9:g.138957014_138957015insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: UBE2D2, ubiquitin conjugating enzyme E2 D2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
UBE2D2 transcript variant 1	NM_003339.3:c.24+15601_24… NM_003339.3:c.24+15601_24+15614del	N/A	Intron Variant
UBE2D2 transcript variant 2	NM_181838.2:c.-64+15009_-… NM_181838.2:c.-64+15009_-64+15022del	N/A	Intron Variant
UBE2D2 transcript variant X2	XM_047417691.1:c.-63-2295… XM_047417691.1:c.-63-22956_-63-22943del	N/A	Intron Variant
UBE2D2 transcript variant X1	XM_047417690.1:c.	N/A	Genic Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₅=	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₁	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)₁₁	ins(T)₂₉
GRCh38.p14 chr 5	NC_000005.10:g.139577405_139577429=	NC_000005.10:g.139577416_139577429del	NC_000005.10:g.139577417_139577429del	NC_000005.10:g.139577418_139577429del	NC_000005.10:g.139577419_139577429del	NC_000005.10:g.139577420_139577429del	NC_000005.10:g.139577421_139577429del	NC_000005.10:g.139577422_139577429del	NC_000005.10:g.139577423_139577429del	NC_000005.10:g.139577424_139577429del	NC_000005.10:g.139577425_139577429del	NC_000005.10:g.139577426_139577429del	NC_000005.10:g.139577427_139577429del	NC_000005.10:g.139577428_139577429del	NC_000005.10:g.139577429del	NC_000005.10:g.139577429dup	NC_000005.10:g.139577428_139577429dup	NC_000005.10:g.139577427_139577429dup	NC_000005.10:g.139577426_139577429dup	NC_000005.10:g.139577425_139577429dup	NC_000005.10:g.139577424_139577429dup	NC_000005.10:g.139577423_139577429dup	NC_000005.10:g.139577422_139577429dup	NC_000005.10:g.139577419_139577429dup	NC_000005.10:g.139577429_139577430insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 5	NC_000005.9:g.138956990_138957014=	NC_000005.9:g.138957001_138957014del	NC_000005.9:g.138957002_138957014del	NC_000005.9:g.138957003_138957014del	NC_000005.9:g.138957004_138957014del	NC_000005.9:g.138957005_138957014del	NC_000005.9:g.138957006_138957014del	NC_000005.9:g.138957007_138957014del	NC_000005.9:g.138957008_138957014del	NC_000005.9:g.138957009_138957014del	NC_000005.9:g.138957010_138957014del	NC_000005.9:g.138957011_138957014del	NC_000005.9:g.138957012_138957014del	NC_000005.9:g.138957013_138957014del	NC_000005.9:g.138957014del	NC_000005.9:g.138957014dup	NC_000005.9:g.138957013_138957014dup	NC_000005.9:g.138957012_138957014dup	NC_000005.9:g.138957011_138957014dup	NC_000005.9:g.138957010_138957014dup	NC_000005.9:g.138957009_138957014dup	NC_000005.9:g.138957008_138957014dup	NC_000005.9:g.138957007_138957014dup	NC_000005.9:g.138957004_138957014dup	NC_000005.9:g.138957014_138957015insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
UBE2D2 transcript variant 1	NM_003339.2:c.24+15590=	NM_003339.2:c.24+15601_24+15614del	NM_003339.2:c.24+15602_24+15614del	NM_003339.2:c.24+15603_24+15614del	NM_003339.2:c.24+15604_24+15614del	NM_003339.2:c.24+15605_24+15614del	NM_003339.2:c.24+15606_24+15614del	NM_003339.2:c.24+15607_24+15614del	NM_003339.2:c.24+15608_24+15614del	NM_003339.2:c.24+15609_24+15614del	NM_003339.2:c.24+15610_24+15614del	NM_003339.2:c.24+15611_24+15614del	NM_003339.2:c.24+15612_24+15614del	NM_003339.2:c.24+15613_24+15614del	NM_003339.2:c.24+15614del	NM_003339.2:c.24+15614dup	NM_003339.2:c.24+15613_24+15614dup	NM_003339.2:c.24+15612_24+15614dup	NM_003339.2:c.24+15611_24+15614dup	NM_003339.2:c.24+15610_24+15614dup	NM_003339.2:c.24+15609_24+15614dup	NM_003339.2:c.24+15608_24+15614dup	NM_003339.2:c.24+15607_24+15614dup	NM_003339.2:c.24+15604_24+15614dup	NM_003339.2:c.24+15614_24+15615insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
UBE2D2 transcript variant 1	NM_003339.3:c.24+15590=	NM_003339.3:c.24+15601_24+15614del	NM_003339.3:c.24+15602_24+15614del	NM_003339.3:c.24+15603_24+15614del	NM_003339.3:c.24+15604_24+15614del	NM_003339.3:c.24+15605_24+15614del	NM_003339.3:c.24+15606_24+15614del	NM_003339.3:c.24+15607_24+15614del	NM_003339.3:c.24+15608_24+15614del	NM_003339.3:c.24+15609_24+15614del	NM_003339.3:c.24+15610_24+15614del	NM_003339.3:c.24+15611_24+15614del	NM_003339.3:c.24+15612_24+15614del	NM_003339.3:c.24+15613_24+15614del	NM_003339.3:c.24+15614del	NM_003339.3:c.24+15614dup	NM_003339.3:c.24+15613_24+15614dup	NM_003339.3:c.24+15612_24+15614dup	NM_003339.3:c.24+15611_24+15614dup	NM_003339.3:c.24+15610_24+15614dup	NM_003339.3:c.24+15609_24+15614dup	NM_003339.3:c.24+15608_24+15614dup	NM_003339.3:c.24+15607_24+15614dup	NM_003339.3:c.24+15604_24+15614dup	NM_003339.3:c.24+15614_24+15615insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
UBE2D2 transcript variant 2	NM_181838.1:c.-64+14998=	NM_181838.1:c.-64+15009_-64+15022del	NM_181838.1:c.-64+15010_-64+15022del	NM_181838.1:c.-64+15011_-64+15022del	NM_181838.1:c.-64+15012_-64+15022del	NM_181838.1:c.-64+15013_-64+15022del	NM_181838.1:c.-64+15014_-64+15022del	NM_181838.1:c.-64+15015_-64+15022del	NM_181838.1:c.-64+15016_-64+15022del	NM_181838.1:c.-64+15017_-64+15022del	NM_181838.1:c.-64+15018_-64+15022del	NM_181838.1:c.-64+15019_-64+15022del	NM_181838.1:c.-64+15020_-64+15022del	NM_181838.1:c.-64+15021_-64+15022del	NM_181838.1:c.-64+15022del	NM_181838.1:c.-64+15022dup	NM_181838.1:c.-64+15021_-64+15022dup	NM_181838.1:c.-64+15020_-64+15022dup	NM_181838.1:c.-64+15019_-64+15022dup	NM_181838.1:c.-64+15018_-64+15022dup	NM_181838.1:c.-64+15017_-64+15022dup	NM_181838.1:c.-64+15016_-64+15022dup	NM_181838.1:c.-64+15015_-64+15022dup	NM_181838.1:c.-64+15012_-64+15022dup	NM_181838.1:c.-64+15022_-64+15023insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
UBE2D2 transcript variant 2	NM_181838.2:c.-64+14998=	NM_181838.2:c.-64+15009_-64+15022del	NM_181838.2:c.-64+15010_-64+15022del	NM_181838.2:c.-64+15011_-64+15022del	NM_181838.2:c.-64+15012_-64+15022del	NM_181838.2:c.-64+15013_-64+15022del	NM_181838.2:c.-64+15014_-64+15022del	NM_181838.2:c.-64+15015_-64+15022del	NM_181838.2:c.-64+15016_-64+15022del	NM_181838.2:c.-64+15017_-64+15022del	NM_181838.2:c.-64+15018_-64+15022del	NM_181838.2:c.-64+15019_-64+15022del	NM_181838.2:c.-64+15020_-64+15022del	NM_181838.2:c.-64+15021_-64+15022del	NM_181838.2:c.-64+15022del	NM_181838.2:c.-64+15022dup	NM_181838.2:c.-64+15021_-64+15022dup	NM_181838.2:c.-64+15020_-64+15022dup	NM_181838.2:c.-64+15019_-64+15022dup	NM_181838.2:c.-64+15018_-64+15022dup	NM_181838.2:c.-64+15017_-64+15022dup	NM_181838.2:c.-64+15016_-64+15022dup	NM_181838.2:c.-64+15015_-64+15022dup	NM_181838.2:c.-64+15012_-64+15022dup	NM_181838.2:c.-64+15022_-64+15023insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
UBE2D2 transcript variant X2	XM_047417691.1:c.-63-22967=	XM_047417691.1:c.-63-22956_-63-22943del	XM_047417691.1:c.-63-22955_-63-22943del	XM_047417691.1:c.-63-22954_-63-22943del	XM_047417691.1:c.-63-22953_-63-22943del	XM_047417691.1:c.-63-22952_-63-22943del	XM_047417691.1:c.-63-22951_-63-22943del	XM_047417691.1:c.-63-22950_-63-22943del	XM_047417691.1:c.-63-22949_-63-22943del	XM_047417691.1:c.-63-22948_-63-22943del	XM_047417691.1:c.-63-22947_-63-22943del	XM_047417691.1:c.-63-22946_-63-22943del	XM_047417691.1:c.-63-22945_-63-22943del	XM_047417691.1:c.-63-22944_-63-22943del	XM_047417691.1:c.-63-22943del	XM_047417691.1:c.-63-22943dup	XM_047417691.1:c.-63-22944_-63-22943dup	XM_047417691.1:c.-63-22945_-63-22943dup	XM_047417691.1:c.-63-22946_-63-22943dup	XM_047417691.1:c.-63-22947_-63-22943dup	XM_047417691.1:c.-63-22948_-63-22943dup	XM_047417691.1:c.-63-22949_-63-22943dup	XM_047417691.1:c.-63-22950_-63-22943dup	XM_047417691.1:c.-63-22953_-63-22943dup	XM_047417691.1:c.-63-22943_-63-22942insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

56 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42559629	Mar 15, 2016 (147)
2	HUMANGENOME_JCVI	ss95408592	Mar 15, 2016 (147)
3	SWEGEN	ss2997881333	Jan 10, 2018 (151)
4	MCHAISSO	ss3065053286	Nov 08, 2017 (151)
5	EVA	ss3829530756	Apr 26, 2020 (154)
6	KOGIC	ss3957751559	Apr 26, 2020 (154)
7	KOGIC	ss3957751560	Apr 26, 2020 (154)
8	KOGIC	ss3957751561	Apr 26, 2020 (154)
9	KOGIC	ss3957751562	Apr 26, 2020 (154)
10	KOGIC	ss3957751563	Apr 26, 2020 (154)
11	KOGIC	ss3957751564	Apr 26, 2020 (154)
12	GNOMAD	ss4130305445	Apr 26, 2021 (155)
13	GNOMAD	ss4130305446	Apr 26, 2021 (155)
14	GNOMAD	ss4130305447	Apr 26, 2021 (155)
15	GNOMAD	ss4130305448	Apr 26, 2021 (155)
16	GNOMAD	ss4130305449	Apr 26, 2021 (155)
17	GNOMAD	ss4130305450	Apr 26, 2021 (155)
18	GNOMAD	ss4130305451	Apr 26, 2021 (155)
19	GNOMAD	ss4130305452	Apr 26, 2021 (155)
20	GNOMAD	ss4130305453	Apr 26, 2021 (155)
21	GNOMAD	ss4130305455	Apr 26, 2021 (155)
22	GNOMAD	ss4130305456	Apr 26, 2021 (155)
23	GNOMAD	ss4130305457	Apr 26, 2021 (155)
24	GNOMAD	ss4130305458	Apr 26, 2021 (155)
25	GNOMAD	ss4130305459	Apr 26, 2021 (155)
26	GNOMAD	ss4130305460	Apr 26, 2021 (155)
27	GNOMAD	ss4130305461	Apr 26, 2021 (155)
28	GNOMAD	ss4130305462	Apr 26, 2021 (155)
29	GNOMAD	ss4130305463	Apr 26, 2021 (155)
30	GNOMAD	ss4130305464	Apr 26, 2021 (155)
31	GNOMAD	ss4130305465	Apr 26, 2021 (155)
32	GNOMAD	ss4130305466	Apr 26, 2021 (155)
33	GNOMAD	ss4130305467	Apr 26, 2021 (155)
34	TOPMED	ss4680672559	Apr 26, 2021 (155)
35	TOPMED	ss4680672560	Apr 26, 2021 (155)
36	TOPMED	ss4680672561	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5174393534	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5174393535	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5174393536	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5174393537	Apr 26, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5266037889	Oct 13, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5266037890	Oct 13, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5266037891	Oct 13, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5266037892	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5463984522	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5463984523	Oct 13, 2022 (156)
47	HUGCELL_USP	ss5463984524	Oct 13, 2022 (156)
48	HUGCELL_USP	ss5463984525	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5711546664	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5711546665	Oct 13, 2022 (156)
51	TOMMO_GENOMICS	ss5711546666	Oct 13, 2022 (156)
52	TOMMO_GENOMICS	ss5711546667	Oct 13, 2022 (156)
53	TOMMO_GENOMICS	ss5711546668	Oct 13, 2022 (156)
54	TOMMO_GENOMICS	ss5711546669	Oct 13, 2022 (156)
55	EVA	ss5835717120	Oct 13, 2022 (156)
56	EVA	ss5835717121	Oct 13, 2022 (156)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 206018725 (NC_000005.10:139577404::T 5516/64640) Row 206018726 (NC_000005.10:139577404::TTT 425/64548) Row 206018727 (NC_000005.10:139577404::TTTT 132/64558)...	-	Apr 26, 2021 (155)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 14129560 (NC_000005.10:139577410:T: 198/1830) Row 14129561 (NC_000005.10:139577411::T 283/1830) Row 14129562 (NC_000005.10:139577411::TT 87/1830)...	-	Apr 26, 2020 (154)
80	Korean Genome Project Submission ignored due to conflicting rows: Row 14129560 (NC_000005.10:139577410:T: 198/1830) Row 14129561 (NC_000005.10:139577411::T 283/1830) Row 14129562 (NC_000005.10:139577411::TT 87/1830)...	-	Apr 26, 2020 (154)
81	Korean Genome Project Submission ignored due to conflicting rows: Row 14129560 (NC_000005.10:139577410:T: 198/1830) Row 14129561 (NC_000005.10:139577411::T 283/1830) Row 14129562 (NC_000005.10:139577411::TT 87/1830)...	-	Apr 26, 2020 (154)
82	Korean Genome Project Submission ignored due to conflicting rows: Row 14129560 (NC_000005.10:139577410:T: 198/1830) Row 14129561 (NC_000005.10:139577411::T 283/1830) Row 14129562 (NC_000005.10:139577411::TT 87/1830)...	-	Apr 26, 2020 (154)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 14129560 (NC_000005.10:139577410:T: 198/1830) Row 14129561 (NC_000005.10:139577411::T 283/1830) Row 14129562 (NC_000005.10:139577411::TT 87/1830)...	-	Apr 26, 2020 (154)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 14129560 (NC_000005.10:139577410:T: 198/1830) Row 14129561 (NC_000005.10:139577411::T 283/1830) Row 14129562 (NC_000005.10:139577411::TT 87/1830)...	-	Apr 26, 2020 (154)
85	8.3KJPN Submission ignored due to conflicting rows: Row 32362841 (NC_000005.9:138956989::T 971/16540) Row 32362842 (NC_000005.9:138956989:T: 353/16540) Row 32362843 (NC_000005.9:138956989:TTTTTTT: 12/16540)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 32362841 (NC_000005.9:138956989::T 971/16540) Row 32362842 (NC_000005.9:138956989:T: 353/16540) Row 32362843 (NC_000005.9:138956989:TTTTTTT: 12/16540)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 32362841 (NC_000005.9:138956989::T 971/16540) Row 32362842 (NC_000005.9:138956989:T: 353/16540) Row 32362843 (NC_000005.9:138956989:TTTTTTT: 12/16540)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 32362841 (NC_000005.9:138956989::T 971/16540) Row 32362842 (NC_000005.9:138956989:T: 353/16540) Row 32362843 (NC_000005.9:138956989:TTTTTTT: 12/16540)...	-	Apr 26, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 45383768 (NC_000005.10:139577404::T 1592/27982) Row 45383769 (NC_000005.10:139577404:T: 684/27982) Row 45383770 (NC_000005.10:139577404:TTTTTTT: 22/27982)...	-	Oct 13, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 45383768 (NC_000005.10:139577404::T 1592/27982) Row 45383769 (NC_000005.10:139577404:T: 684/27982) Row 45383770 (NC_000005.10:139577404:TTTTTTT: 22/27982)...	-	Oct 13, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 45383768 (NC_000005.10:139577404::T 1592/27982) Row 45383769 (NC_000005.10:139577404:T: 684/27982) Row 45383770 (NC_000005.10:139577404:TTTTTTT: 22/27982)...	-	Oct 13, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 45383768 (NC_000005.10:139577404::T 1592/27982) Row 45383769 (NC_000005.10:139577404:T: 684/27982) Row 45383770 (NC_000005.10:139577404:TTTTTTT: 22/27982)...	-	Oct 13, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 45383768 (NC_000005.10:139577404::T 1592/27982) Row 45383769 (NC_000005.10:139577404:T: 684/27982) Row 45383770 (NC_000005.10:139577404:TTTTTTT: 22/27982)...	-	Oct 13, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 45383768 (NC_000005.10:139577404::T 1592/27982) Row 45383769 (NC_000005.10:139577404:T: 684/27982) Row 45383770 (NC_000005.10:139577404:TTTTTTT: 22/27982)...	-	Oct 13, 2022 (156)
95	TopMed Submission ignored due to conflicting rows: Row 518050116 (NC_000005.10:139577404:TTTTTTT: 91/264690) Row 518050117 (NC_000005.10:139577404:TTTTTTTTTT: 9/264690) Row 518050118 (NC_000005.10:139577404:TTTTTTTTTTTTT: 8/264690)	-	Apr 26, 2021 (155)
96	TopMed Submission ignored due to conflicting rows: Row 518050116 (NC_000005.10:139577404:TTTTTTT: 91/264690) Row 518050117 (NC_000005.10:139577404:TTTTTTTTTT: 9/264690) Row 518050118 (NC_000005.10:139577404:TTTTTTTTTTTTT: 8/264690)	-	Apr 26, 2021 (155)
97	TopMed Submission ignored due to conflicting rows: Row 518050116 (NC_000005.10:139577404:TTTTTTT: 91/264690) Row 518050117 (NC_000005.10:139577404:TTTTTTTTTT: 9/264690) Row 518050118 (NC_000005.10:139577404:TTTTTTTTTTTTT: 8/264690)	-	Apr 26, 2021 (155)
98	ALFA	NC_000005.10 - 139577405	Apr 26, 2021 (155)

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

Associated ID	History Updated (Build)
rs35460807	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4130305467, ss4680672561	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4130305466	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4130305465	NC_000005.10:139577404:TTTTTTTTTTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4130305464, ss4680672560	NC_000005.10:139577404:TTTTTTTTTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4130305463	NC_000005.10:139577404:TTTTTTTTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4130305462	NC_000005.10:139577404:TTTTTTTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5174393536	NC_000005.9:138956989:TTTTTTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3957751563, ss4130305461, ss4680672559, ss5266037891, ss5711546666	NC_000005.10:139577404:TTTTTTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4130305460	NC_000005.10:139577404:TTTTTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4130305459	NC_000005.10:139577404:TTTTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4130305458, ss5266037892	NC_000005.10:139577404:TTTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4130305457, ss5266037889	NC_000005.10:139577404:TTT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss2997881333	NC_000005.9:138956989:TT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4130305456, ss5266037890, ss5463984525	NC_000005.10:139577404:TT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3957751564	NC_000005.10:139577409:TT:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3829530756, ss5174393535	NC_000005.9:138956989:T:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4130305455, ss5463984522, ss5711546665	NC_000005.10:139577404:T:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3957751559	NC_000005.10:139577410:T:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss42559629, ss95408592	NT_029289.11:119940:T:	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5174393534	NC_000005.9:138956989::T	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4130305445, ss5463984523, ss5711546664	NC_000005.10:139577404::T	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3957751560	NC_000005.10:139577411::T	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5174393537, ss5835717121	NC_000005.9:138956989::TT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3065053286, ss5463984524, ss5711546667	NC_000005.10:139577404::TT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3957751561	NC_000005.10:139577411::TT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5835717120	NC_000005.9:138956989::TTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
ss4130305446, ss5711546668	NC_000005.10:139577404::TTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3957751562	NC_000005.10:139577411::TTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4130305447	NC_000005.10:139577404::TTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4130305448, ss5711546669	NC_000005.10:139577404::TTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4130305449	NC_000005.10:139577404::TTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4130305450	NC_000005.10:139577404::TTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11642521132	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4130305451	NC_000005.10:139577404::TTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4130305452	NC_000005.10:139577404::TTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4130305453	NC_000005.10:139577404::TTTTTTTTTT… NC_000005.10:139577404::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000005.10:139577404:TTTTTTTTTTT… NC_000005.10:139577404:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs869189901

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs869189901