Name: rs897311922
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.

rs897311922

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:42195501-42195517 (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)₇ / del(T)₅ / del(T)₄ / delT…
del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dup(T)₅ / dup(T)₆
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.00115 (21/18262, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TCF20 : 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	HTRZ	HWEP
Total	Global	18262	TTTTTTTTTTTTTTTTT=0.99869	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00016, TTTTTTTTTTTTTTTTTT=0.00115, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.997699	0.002301	0
European	Sub	14020	TTTTTTTTTTTTTTTTT=0.99829	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00021, TTTTTTTTTTTTTTTTTT=0.00150, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.997003	0.002997	0
African	Sub	2800	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	N/A
African Others	Sub	104	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	N/A
African American	Sub	2696	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	N/A
Asian	Sub	106	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	N/A
East Asian	Sub	84	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
Other Asian	Sub	22	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
Latin American 1	Sub	142	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	N/A
Latin American 2	Sub	602	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	N/A
South Asian	Sub	98	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	N/A
Other	Sub	494	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	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	18262	(T)₁₇=0.99869	del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00016, dupT=0.00115, dupTT=0.00000, dup(T)₆=0.00000
Allele Frequency Aggregator	European	Sub	14020	(T)₁₇=0.99829	del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00021, dupT=0.00150, dupTT=0.00000, dup(T)₆=0.00000
Allele Frequency Aggregator	African	Sub	2800	(T)₁₇=1.0000	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, dup(T)₆=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	602	(T)₁₇=1.000	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, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	494	(T)₁₇=1.000	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, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	142	(T)₁₇=1.000	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, dup(T)₆=0.000
Allele Frequency Aggregator	Asian	Sub	106	(T)₁₇=1.000	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, dup(T)₆=0.000
Allele Frequency Aggregator	South Asian	Sub	98	(T)₁₇=1.00	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, dup(T)₆=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 22	NC_000022.11:g.42195511_42195517del
GRCh38.p14 chr 22	NC_000022.11:g.42195513_42195517del
GRCh38.p14 chr 22	NC_000022.11:g.42195514_42195517del
GRCh38.p14 chr 22	NC_000022.11:g.42195515_42195517del
GRCh38.p14 chr 22	NC_000022.11:g.42195516_42195517del
GRCh38.p14 chr 22	NC_000022.11:g.42195517del
GRCh38.p14 chr 22	NC_000022.11:g.42195517dup
GRCh38.p14 chr 22	NC_000022.11:g.42195516_42195517dup
GRCh38.p14 chr 22	NC_000022.11:g.42195513_42195517dup
GRCh38.p14 chr 22	NC_000022.11:g.42195512_42195517dup
GRCh37.p13 chr 22	NC_000022.10:g.42591517_42591523del
GRCh37.p13 chr 22	NC_000022.10:g.42591519_42591523del
GRCh37.p13 chr 22	NC_000022.10:g.42591520_42591523del
GRCh37.p13 chr 22	NC_000022.10:g.42591521_42591523del
GRCh37.p13 chr 22	NC_000022.10:g.42591522_42591523del
GRCh37.p13 chr 22	NC_000022.10:g.42591523del
GRCh37.p13 chr 22	NC_000022.10:g.42591523dup
GRCh37.p13 chr 22	NC_000022.10:g.42591522_42591523dup
GRCh37.p13 chr 22	NC_000022.10:g.42591519_42591523dup
GRCh37.p13 chr 22	NC_000022.10:g.42591518_42591523dup
TCF20 RefSeqGene (LRG_1025)	NG_028982.3:g.153110_153116del
TCF20 RefSeqGene (LRG_1025)	NG_028982.3:g.153112_153116del
TCF20 RefSeqGene (LRG_1025)	NG_028982.3:g.153113_153116del
TCF20 RefSeqGene (LRG_1025)	NG_028982.3:g.153114_153116del
TCF20 RefSeqGene (LRG_1025)	NG_028982.3:g.153115_153116del
TCF20 RefSeqGene (LRG_1025)	NG_028982.3:g.153116del
TCF20 RefSeqGene (LRG_1025)	NG_028982.3:g.153116dup
TCF20 RefSeqGene (LRG_1025)	NG_028982.3:g.153115_153116dup
TCF20 RefSeqGene (LRG_1025)	NG_028982.3:g.153112_153116dup
TCF20 RefSeqGene (LRG_1025)	NG_028982.3:g.153111_153116dup
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG1	NW_003315971.2:g.105703_105709del
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG1	NW_003315971.2:g.105705_105709del
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG1	NW_003315971.2:g.105706_105709del
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG1	NW_003315971.2:g.105707_105709del
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG1	NW_003315971.2:g.105708_105709del
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG1	NW_003315971.2:g.105709del
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG1	NW_003315971.2:g.105709dup
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG1	NW_003315971.2:g.105708_105709dup
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG1	NW_003315971.2:g.105705_105709dup
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG1	NW_003315971.2:g.105704_105709dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.117856_117862del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.117858_117862del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.117859_117862del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.117860_117862del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.117861_117862del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.117862del
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.117862dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.117861_117862dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.117858_117862dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.117857_117862dup
GRCh38.p14 chr 22 novel patch HSCHR22_4_CTG1	NW_009646207.1:g.98315_98321del
GRCh38.p14 chr 22 novel patch HSCHR22_4_CTG1	NW_009646207.1:g.98317_98321del
GRCh38.p14 chr 22 novel patch HSCHR22_4_CTG1	NW_009646207.1:g.98318_98321del
GRCh38.p14 chr 22 novel patch HSCHR22_4_CTG1	NW_009646207.1:g.98319_98321del
GRCh38.p14 chr 22 novel patch HSCHR22_4_CTG1	NW_009646207.1:g.98320_98321del
GRCh38.p14 chr 22 novel patch HSCHR22_4_CTG1	NW_009646207.1:g.98321del
GRCh38.p14 chr 22 novel patch HSCHR22_4_CTG1	NW_009646207.1:g.98321dup
GRCh38.p14 chr 22 novel patch HSCHR22_4_CTG1	NW_009646207.1:g.98320_98321dup
GRCh38.p14 chr 22 novel patch HSCHR22_4_CTG1	NW_009646207.1:g.98317_98321dup
GRCh38.p14 chr 22 novel patch HSCHR22_4_CTG1	NW_009646207.1:g.98316_98321dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.116502_116508del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.116504_116508del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.116505_116508del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.116506_116508del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.116507_116508del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.116508del
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.116508dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.116507_116508dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.116504_116508dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.116503_116508dup
GRCh38.p14 chr 22 novel patch HSCHR22_6_CTG1	NW_014040930.1:g.97683_97689del
GRCh38.p14 chr 22 novel patch HSCHR22_6_CTG1	NW_014040930.1:g.97685_97689del
GRCh38.p14 chr 22 novel patch HSCHR22_6_CTG1	NW_014040930.1:g.97686_97689del
GRCh38.p14 chr 22 novel patch HSCHR22_6_CTG1	NW_014040930.1:g.97687_97689del
GRCh38.p14 chr 22 novel patch HSCHR22_6_CTG1	NW_014040930.1:g.97688_97689del
GRCh38.p14 chr 22 novel patch HSCHR22_6_CTG1	NW_014040930.1:g.97689del
GRCh38.p14 chr 22 novel patch HSCHR22_6_CTG1	NW_014040930.1:g.97689dup
GRCh38.p14 chr 22 novel patch HSCHR22_6_CTG1	NW_014040930.1:g.97688_97689dup
GRCh38.p14 chr 22 novel patch HSCHR22_6_CTG1	NW_014040930.1:g.97685_97689dup
GRCh38.p14 chr 22 novel patch HSCHR22_6_CTG1	NW_014040930.1:g.97684_97689dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.94780_94786del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.94782_94786del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.94783_94786del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.94784_94786del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.94785_94786del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.94786del
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.94786dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.94785_94786dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.94782_94786dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.94781_94786dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.86915_86921del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.86917_86921del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.86918_86921del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.86919_86921del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.86920_86921del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.86921del
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.86921dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.86920_86921dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.86917_86921dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.86916_86921dup

Gene: TCF20, transcription factor 20 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TCF20 transcript variant 3	NM_001378418.1:c.5655+141… NM_001378418.1:c.5655+14144_5655+14150del	N/A	Intron Variant
TCF20 transcript variant 1	NM_005650.4:c.5655+14144_… NM_005650.4:c.5655+14144_5655+14150del	N/A	Intron Variant
TCF20 transcript variant 2	NM_181492.3:c.5655+14144_… NM_181492.3:c.5655+14144_5655+14150del	N/A	Intron Variant
TCF20 transcript variant X1	XM_005261722.4:c.5655+141… XM_005261722.4:c.5655+14144_5655+14150del	N/A	Intron Variant
TCF20 transcript variant X4	XM_011530353.3:c.5655+141… XM_011530353.3:c.5655+14144_5655+14150del	N/A	Intron Variant
TCF20 transcript variant X2	XM_047441474.1:c.5655+141… XM_047441474.1:c.5655+14144_5655+14150del	N/A	Intron Variant
TCF20 transcript variant X3	XM_047441475.1:c.5655+141… XM_047441475.1:c.5655+14144_5655+14150del	N/A	Intron Variant
TCF20 transcript variant X5	XM_047441476.1:c.5655+141… XM_047441476.1:c.5655+14144_5655+14150del	N/A	Intron Variant
TCF20 transcript variant X6	XM_047441477.1:c.5655+141… XM_047441477.1:c.5655+14144_5655+14150del	N/A	Intron Variant
TCF20 transcript variant X7	XM_047441478.1:c.5655+141… XM_047441478.1:c.5655+14144_5655+14150del	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)₁₇=	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dup(T)₅	dup(T)₆
GRCh38.p14 chr 22	NC_000022.11:g.42195501_42195517=	NC_000022.11:g.42195511_42195517del	NC_000022.11:g.42195513_42195517del	NC_000022.11:g.42195514_42195517del	NC_000022.11:g.42195515_42195517del	NC_000022.11:g.42195516_42195517del	NC_000022.11:g.42195517del	NC_000022.11:g.42195517dup	NC_000022.11:g.42195516_42195517dup	NC_000022.11:g.42195513_42195517dup	NC_000022.11:g.42195512_42195517dup
GRCh37.p13 chr 22	NC_000022.10:g.42591507_42591523=	NC_000022.10:g.42591517_42591523del	NC_000022.10:g.42591519_42591523del	NC_000022.10:g.42591520_42591523del	NC_000022.10:g.42591521_42591523del	NC_000022.10:g.42591522_42591523del	NC_000022.10:g.42591523del	NC_000022.10:g.42591523dup	NC_000022.10:g.42591522_42591523dup	NC_000022.10:g.42591519_42591523dup	NC_000022.10:g.42591518_42591523dup
TCF20 RefSeqGene (LRG_1025)	NG_028982.3:g.153100_153116=	NG_028982.3:g.153110_153116del	NG_028982.3:g.153112_153116del	NG_028982.3:g.153113_153116del	NG_028982.3:g.153114_153116del	NG_028982.3:g.153115_153116del	NG_028982.3:g.153116del	NG_028982.3:g.153116dup	NG_028982.3:g.153115_153116dup	NG_028982.3:g.153112_153116dup	NG_028982.3:g.153111_153116dup
GRCh38.p14 chr 22 alt locus HSCHR22_1_CTG1	NW_003315971.2:g.105693_105709=	NW_003315971.2:g.105703_105709del	NW_003315971.2:g.105705_105709del	NW_003315971.2:g.105706_105709del	NW_003315971.2:g.105707_105709del	NW_003315971.2:g.105708_105709del	NW_003315971.2:g.105709del	NW_003315971.2:g.105709dup	NW_003315971.2:g.105708_105709dup	NW_003315971.2:g.105705_105709dup	NW_003315971.2:g.105704_105709dup
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1	NT_187682.1:g.117846_117862=	NT_187682.1:g.117856_117862del	NT_187682.1:g.117858_117862del	NT_187682.1:g.117859_117862del	NT_187682.1:g.117860_117862del	NT_187682.1:g.117861_117862del	NT_187682.1:g.117862del	NT_187682.1:g.117862dup	NT_187682.1:g.117861_117862dup	NT_187682.1:g.117858_117862dup	NT_187682.1:g.117857_117862dup
GRCh38.p14 chr 22 novel patch HSCHR22_4_CTG1	NW_009646207.1:g.98305_98321=	NW_009646207.1:g.98315_98321del	NW_009646207.1:g.98317_98321del	NW_009646207.1:g.98318_98321del	NW_009646207.1:g.98319_98321del	NW_009646207.1:g.98320_98321del	NW_009646207.1:g.98321del	NW_009646207.1:g.98321dup	NW_009646207.1:g.98320_98321dup	NW_009646207.1:g.98317_98321dup	NW_009646207.1:g.98316_98321dup
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1	NW_014040931.1:g.116492_116508=	NW_014040931.1:g.116502_116508del	NW_014040931.1:g.116504_116508del	NW_014040931.1:g.116505_116508del	NW_014040931.1:g.116506_116508del	NW_014040931.1:g.116507_116508del	NW_014040931.1:g.116508del	NW_014040931.1:g.116508dup	NW_014040931.1:g.116507_116508dup	NW_014040931.1:g.116504_116508dup	NW_014040931.1:g.116503_116508dup
GRCh38.p14 chr 22 novel patch HSCHR22_6_CTG1	NW_014040930.1:g.97673_97689=	NW_014040930.1:g.97683_97689del	NW_014040930.1:g.97685_97689del	NW_014040930.1:g.97686_97689del	NW_014040930.1:g.97687_97689del	NW_014040930.1:g.97688_97689del	NW_014040930.1:g.97689del	NW_014040930.1:g.97689dup	NW_014040930.1:g.97688_97689dup	NW_014040930.1:g.97685_97689dup	NW_014040930.1:g.97684_97689dup
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1	NW_009646208.1:g.94770_94786=	NW_009646208.1:g.94780_94786del	NW_009646208.1:g.94782_94786del	NW_009646208.1:g.94783_94786del	NW_009646208.1:g.94784_94786del	NW_009646208.1:g.94785_94786del	NW_009646208.1:g.94786del	NW_009646208.1:g.94786dup	NW_009646208.1:g.94785_94786dup	NW_009646208.1:g.94782_94786dup	NW_009646208.1:g.94781_94786dup
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1	NW_015148968.1:g.86905_86921=	NW_015148968.1:g.86915_86921del	NW_015148968.1:g.86917_86921del	NW_015148968.1:g.86918_86921del	NW_015148968.1:g.86919_86921del	NW_015148968.1:g.86920_86921del	NW_015148968.1:g.86921del	NW_015148968.1:g.86921dup	NW_015148968.1:g.86920_86921dup	NW_015148968.1:g.86917_86921dup	NW_015148968.1:g.86916_86921dup
TCF20 transcript variant 3	NM_001378418.1:c.5655+14150=	NM_001378418.1:c.5655+14144_5655+14150del	NM_001378418.1:c.5655+14146_5655+14150del	NM_001378418.1:c.5655+14147_5655+14150del	NM_001378418.1:c.5655+14148_5655+14150del	NM_001378418.1:c.5655+14149_5655+14150del	NM_001378418.1:c.5655+14150del	NM_001378418.1:c.5655+14150dup	NM_001378418.1:c.5655+14149_5655+14150dup	NM_001378418.1:c.5655+14146_5655+14150dup	NM_001378418.1:c.5655+14145_5655+14150dup
TCF20 transcript variant 1	NM_005650.2:c.5655+14150=	NM_005650.2:c.5655+14144_5655+14150del	NM_005650.2:c.5655+14146_5655+14150del	NM_005650.2:c.5655+14147_5655+14150del	NM_005650.2:c.5655+14148_5655+14150del	NM_005650.2:c.5655+14149_5655+14150del	NM_005650.2:c.5655+14150del	NM_005650.2:c.5655+14150dup	NM_005650.2:c.5655+14149_5655+14150dup	NM_005650.2:c.5655+14146_5655+14150dup	NM_005650.2:c.5655+14145_5655+14150dup
TCF20 transcript variant 1	NM_005650.4:c.5655+14150=	NM_005650.4:c.5655+14144_5655+14150del	NM_005650.4:c.5655+14146_5655+14150del	NM_005650.4:c.5655+14147_5655+14150del	NM_005650.4:c.5655+14148_5655+14150del	NM_005650.4:c.5655+14149_5655+14150del	NM_005650.4:c.5655+14150del	NM_005650.4:c.5655+14150dup	NM_005650.4:c.5655+14149_5655+14150dup	NM_005650.4:c.5655+14146_5655+14150dup	NM_005650.4:c.5655+14145_5655+14150dup
TCF20 transcript variant 2	NM_181492.2:c.5655+14150=	NM_181492.2:c.5655+14144_5655+14150del	NM_181492.2:c.5655+14146_5655+14150del	NM_181492.2:c.5655+14147_5655+14150del	NM_181492.2:c.5655+14148_5655+14150del	NM_181492.2:c.5655+14149_5655+14150del	NM_181492.2:c.5655+14150del	NM_181492.2:c.5655+14150dup	NM_181492.2:c.5655+14149_5655+14150dup	NM_181492.2:c.5655+14146_5655+14150dup	NM_181492.2:c.5655+14145_5655+14150dup
TCF20 transcript variant 2	NM_181492.3:c.5655+14150=	NM_181492.3:c.5655+14144_5655+14150del	NM_181492.3:c.5655+14146_5655+14150del	NM_181492.3:c.5655+14147_5655+14150del	NM_181492.3:c.5655+14148_5655+14150del	NM_181492.3:c.5655+14149_5655+14150del	NM_181492.3:c.5655+14150del	NM_181492.3:c.5655+14150dup	NM_181492.3:c.5655+14149_5655+14150dup	NM_181492.3:c.5655+14146_5655+14150dup	NM_181492.3:c.5655+14145_5655+14150dup
TCF20 transcript variant X1	XM_005261722.1:c.5655+14150=	XM_005261722.1:c.5655+14144_5655+14150del	XM_005261722.1:c.5655+14146_5655+14150del	XM_005261722.1:c.5655+14147_5655+14150del	XM_005261722.1:c.5655+14148_5655+14150del	XM_005261722.1:c.5655+14149_5655+14150del	XM_005261722.1:c.5655+14150del	XM_005261722.1:c.5655+14150dup	XM_005261722.1:c.5655+14149_5655+14150dup	XM_005261722.1:c.5655+14146_5655+14150dup	XM_005261722.1:c.5655+14145_5655+14150dup
TCF20 transcript variant X1	XM_005261722.4:c.5655+14150=	XM_005261722.4:c.5655+14144_5655+14150del	XM_005261722.4:c.5655+14146_5655+14150del	XM_005261722.4:c.5655+14147_5655+14150del	XM_005261722.4:c.5655+14148_5655+14150del	XM_005261722.4:c.5655+14149_5655+14150del	XM_005261722.4:c.5655+14150del	XM_005261722.4:c.5655+14150dup	XM_005261722.4:c.5655+14149_5655+14150dup	XM_005261722.4:c.5655+14146_5655+14150dup	XM_005261722.4:c.5655+14145_5655+14150dup
TCF20 transcript variant X2	XM_005261723.1:c.5655+14150=	XM_005261723.1:c.5655+14144_5655+14150del	XM_005261723.1:c.5655+14146_5655+14150del	XM_005261723.1:c.5655+14147_5655+14150del	XM_005261723.1:c.5655+14148_5655+14150del	XM_005261723.1:c.5655+14149_5655+14150del	XM_005261723.1:c.5655+14150del	XM_005261723.1:c.5655+14150dup	XM_005261723.1:c.5655+14149_5655+14150dup	XM_005261723.1:c.5655+14146_5655+14150dup	XM_005261723.1:c.5655+14145_5655+14150dup
TCF20 transcript variant X3	XM_005261724.1:c.5655+14150=	XM_005261724.1:c.5655+14144_5655+14150del	XM_005261724.1:c.5655+14146_5655+14150del	XM_005261724.1:c.5655+14147_5655+14150del	XM_005261724.1:c.5655+14148_5655+14150del	XM_005261724.1:c.5655+14149_5655+14150del	XM_005261724.1:c.5655+14150del	XM_005261724.1:c.5655+14150dup	XM_005261724.1:c.5655+14149_5655+14150dup	XM_005261724.1:c.5655+14146_5655+14150dup	XM_005261724.1:c.5655+14145_5655+14150dup
TCF20 transcript variant X4	XM_011530353.3:c.5655+14150=	XM_011530353.3:c.5655+14144_5655+14150del	XM_011530353.3:c.5655+14146_5655+14150del	XM_011530353.3:c.5655+14147_5655+14150del	XM_011530353.3:c.5655+14148_5655+14150del	XM_011530353.3:c.5655+14149_5655+14150del	XM_011530353.3:c.5655+14150del	XM_011530353.3:c.5655+14150dup	XM_011530353.3:c.5655+14149_5655+14150dup	XM_011530353.3:c.5655+14146_5655+14150dup	XM_011530353.3:c.5655+14145_5655+14150dup
TCF20 transcript variant X2	XM_047441474.1:c.5655+14150=	XM_047441474.1:c.5655+14144_5655+14150del	XM_047441474.1:c.5655+14146_5655+14150del	XM_047441474.1:c.5655+14147_5655+14150del	XM_047441474.1:c.5655+14148_5655+14150del	XM_047441474.1:c.5655+14149_5655+14150del	XM_047441474.1:c.5655+14150del	XM_047441474.1:c.5655+14150dup	XM_047441474.1:c.5655+14149_5655+14150dup	XM_047441474.1:c.5655+14146_5655+14150dup	XM_047441474.1:c.5655+14145_5655+14150dup
TCF20 transcript variant X3	XM_047441475.1:c.5655+14150=	XM_047441475.1:c.5655+14144_5655+14150del	XM_047441475.1:c.5655+14146_5655+14150del	XM_047441475.1:c.5655+14147_5655+14150del	XM_047441475.1:c.5655+14148_5655+14150del	XM_047441475.1:c.5655+14149_5655+14150del	XM_047441475.1:c.5655+14150del	XM_047441475.1:c.5655+14150dup	XM_047441475.1:c.5655+14149_5655+14150dup	XM_047441475.1:c.5655+14146_5655+14150dup	XM_047441475.1:c.5655+14145_5655+14150dup
TCF20 transcript variant X5	XM_047441476.1:c.5655+14150=	XM_047441476.1:c.5655+14144_5655+14150del	XM_047441476.1:c.5655+14146_5655+14150del	XM_047441476.1:c.5655+14147_5655+14150del	XM_047441476.1:c.5655+14148_5655+14150del	XM_047441476.1:c.5655+14149_5655+14150del	XM_047441476.1:c.5655+14150del	XM_047441476.1:c.5655+14150dup	XM_047441476.1:c.5655+14149_5655+14150dup	XM_047441476.1:c.5655+14146_5655+14150dup	XM_047441476.1:c.5655+14145_5655+14150dup
TCF20 transcript variant X6	XM_047441477.1:c.5655+14150=	XM_047441477.1:c.5655+14144_5655+14150del	XM_047441477.1:c.5655+14146_5655+14150del	XM_047441477.1:c.5655+14147_5655+14150del	XM_047441477.1:c.5655+14148_5655+14150del	XM_047441477.1:c.5655+14149_5655+14150del	XM_047441477.1:c.5655+14150del	XM_047441477.1:c.5655+14150dup	XM_047441477.1:c.5655+14149_5655+14150dup	XM_047441477.1:c.5655+14146_5655+14150dup	XM_047441477.1:c.5655+14145_5655+14150dup
TCF20 transcript variant X7	XM_047441478.1:c.5655+14150=	XM_047441478.1:c.5655+14144_5655+14150del	XM_047441478.1:c.5655+14146_5655+14150del	XM_047441478.1:c.5655+14147_5655+14150del	XM_047441478.1:c.5655+14148_5655+14150del	XM_047441478.1:c.5655+14149_5655+14150del	XM_047441478.1:c.5655+14150del	XM_047441478.1:c.5655+14150dup	XM_047441478.1:c.5655+14149_5655+14150dup	XM_047441478.1:c.5655+14146_5655+14150dup	XM_047441478.1:c.5655+14145_5655+14150dup

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#.

25 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3019376594	Nov 08, 2017 (151)
2	PACBIO	ss3788838089	Jul 13, 2019 (153)
3	GNOMAD	ss4365379963	Apr 26, 2021 (155)
4	GNOMAD	ss4365379964	Apr 26, 2021 (155)
5	GNOMAD	ss4365379965	Apr 26, 2021 (155)
6	GNOMAD	ss4365379966	Apr 26, 2021 (155)
7	GNOMAD	ss4365379967	Apr 26, 2021 (155)
8	GNOMAD	ss4365379968	Apr 26, 2021 (155)
9	GNOMAD	ss4365379969	Apr 26, 2021 (155)
10	GNOMAD	ss4365379970	Apr 26, 2021 (155)
11	TOPMED	ss5110801387	Apr 26, 2021 (155)
12	TOPMED	ss5110801390	Apr 26, 2021 (155)
13	TOPMED	ss5110801391	Apr 26, 2021 (155)
14	TOMMO_GENOMICS	ss5232840161	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5232840162	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5232840163	Apr 26, 2021 (155)
17	1000G_HIGH_COVERAGE	ss5311257759	Oct 16, 2022 (156)
18	1000G_HIGH_COVERAGE	ss5311257760	Oct 16, 2022 (156)
19	1000G_HIGH_COVERAGE	ss5311257761	Oct 16, 2022 (156)
20	HUGCELL_USP	ss5503084364	Oct 16, 2022 (156)
21	HUGCELL_USP	ss5503084365	Oct 16, 2022 (156)
22	TOMMO_GENOMICS	ss5794032979	Oct 16, 2022 (156)
23	TOMMO_GENOMICS	ss5794032980	Oct 16, 2022 (156)
24	TOMMO_GENOMICS	ss5794032981	Oct 16, 2022 (156)
25	EVA	ss5853410146	Oct 16, 2022 (156)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571287085 (NC_000022.11:42195500::T 801/130204) Row 571287086 (NC_000022.11:42195500::TT 9/130218) Row 571287087 (NC_000022.11:42195500::TTTTT 1/130222)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571287085 (NC_000022.11:42195500::T 801/130204) Row 571287086 (NC_000022.11:42195500::TT 9/130218) Row 571287087 (NC_000022.11:42195500::TTTTT 1/130222)...	-	Apr 26, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571287085 (NC_000022.11:42195500::T 801/130204) Row 571287086 (NC_000022.11:42195500::TT 9/130218) Row 571287087 (NC_000022.11:42195500::TTTTT 1/130222)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571287085 (NC_000022.11:42195500::T 801/130204) Row 571287086 (NC_000022.11:42195500::TT 9/130218) Row 571287087 (NC_000022.11:42195500::TTTTT 1/130222)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571287085 (NC_000022.11:42195500::T 801/130204) Row 571287086 (NC_000022.11:42195500::TT 9/130218) Row 571287087 (NC_000022.11:42195500::TTTTT 1/130222)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571287085 (NC_000022.11:42195500::T 801/130204) Row 571287086 (NC_000022.11:42195500::TT 9/130218) Row 571287087 (NC_000022.11:42195500::TTTTT 1/130222)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571287085 (NC_000022.11:42195500::T 801/130204) Row 571287086 (NC_000022.11:42195500::TT 9/130218) Row 571287087 (NC_000022.11:42195500::TTTTT 1/130222)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571287085 (NC_000022.11:42195500::T 801/130204) Row 571287086 (NC_000022.11:42195500::TT 9/130218) Row 571287087 (NC_000022.11:42195500::TTTTT 1/130222)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 571287085 (NC_000022.11:42195500::T 801/130204) Row 571287086 (NC_000022.11:42195500::TT 9/130218) Row 571287087 (NC_000022.11:42195500::TTTTT 1/130222)...	-	Apr 26, 2021 (155)
35	8.3KJPN Submission ignored due to conflicting rows: Row 90809468 (NC_000022.10:42591506::T 116/16758) Row 90809469 (NC_000022.10:42591506:T: 23/16758) Row 90809470 (NC_000022.10:42591506:TTTT: 2/16758)	-	Apr 26, 2021 (155)
36	8.3KJPN Submission ignored due to conflicting rows: Row 90809468 (NC_000022.10:42591506::T 116/16758) Row 90809469 (NC_000022.10:42591506:T: 23/16758) Row 90809470 (NC_000022.10:42591506:TTTT: 2/16758)	-	Apr 26, 2021 (155)
37	8.3KJPN Submission ignored due to conflicting rows: Row 90809468 (NC_000022.10:42591506::T 116/16758) Row 90809469 (NC_000022.10:42591506:T: 23/16758) Row 90809470 (NC_000022.10:42591506:TTTT: 2/16758)	-	Apr 26, 2021 (155)
38	14KJPN Submission ignored due to conflicting rows: Row 127870083 (NC_000022.11:42195500:T: 33/28258) Row 127870084 (NC_000022.11:42195500::T 214/28258) Row 127870085 (NC_000022.11:42195500:TTTT: 2/28258)	-	Oct 16, 2022 (156)
39	14KJPN Submission ignored due to conflicting rows: Row 127870083 (NC_000022.11:42195500:T: 33/28258) Row 127870084 (NC_000022.11:42195500::T 214/28258) Row 127870085 (NC_000022.11:42195500:TTTT: 2/28258)	-	Oct 16, 2022 (156)
40	14KJPN Submission ignored due to conflicting rows: Row 127870083 (NC_000022.11:42195500:T: 33/28258) Row 127870084 (NC_000022.11:42195500::T 214/28258) Row 127870085 (NC_000022.11:42195500:TTTT: 2/28258)	-	Oct 16, 2022 (156)
41	TopMed Submission ignored due to conflicting rows: Row 385910334 (NC_000022.11:42195500::TTTTTT 1/264690) Row 385910337 (NC_000022.11:42195500:TTTT: 15/264690) Row 385910338 (NC_000022.11:42195500:TTTTT: 8/264690)	-	Apr 26, 2021 (155)
42	TopMed Submission ignored due to conflicting rows: Row 385910334 (NC_000022.11:42195500::TTTTTT 1/264690) Row 385910337 (NC_000022.11:42195500:TTTT: 15/264690) Row 385910338 (NC_000022.11:42195500:TTTTT: 8/264690)	-	Apr 26, 2021 (155)
43	TopMed Submission ignored due to conflicting rows: Row 385910334 (NC_000022.11:42195500::TTTTTT 1/264690) Row 385910337 (NC_000022.11:42195500:TTTT: 15/264690) Row 385910338 (NC_000022.11:42195500:TTTTT: 8/264690)	-	Apr 26, 2021 (155)
44	ALFA	NC_000022.11 - 42195501	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
ss4365379970	NC_000022.11:42195500:TTTTTTT:	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4365379969, ss5110801391	NC_000022.11:42195500:TTTTT:	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
2406811122	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5232840163	NC_000022.10:42591506:TTTT:	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4365379968, ss5110801390, ss5794032981	NC_000022.11:42195500:TTTT:	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
2406811122	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4365379967, ss5311257761	NC_000022.11:42195500:TTT:	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
2406811122	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4365379966	NC_000022.11:42195500:TT:	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
2406811122	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3019376594, ss3788838089, ss5232840162	NC_000022.10:42591506:T:	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5311257759, ss5503084365, ss5794032979, ss5853410146	NC_000022.11:42195500:T:	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2406811122	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5232840161	NC_000022.10:42591506::T	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4365379963, ss5311257760, ss5503084364, ss5794032980	NC_000022.11:42195500::T	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
2406811122	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4365379964	NC_000022.11:42195500::TT	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2406811122	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4365379965	NC_000022.11:42195500::TTTTT	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5110801387	NC_000022.11:42195500::TTTTTT	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
2406811122	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2414681562	NC_000022.10:42591506:TTT:	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT
ss2414681564	NC_000022.10:42591506:TTTTT:	NC_000022.11:42195500:TTTTTTTTTTTT… NC_000022.11:42195500:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT

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

No publications for rs897311922

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

Genome context:

Select flank length:

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

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs897311922