Name: rs765176193
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.

rs765176193

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:167465328-167465345 (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)₁₁ / del(T)₈ / del(T)₇ / del…
del(T)₁₁ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / 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 / dup(T)₁₁ / dup(T)₁₆ / dup(T)₁₇ / dup(T)₁₈ / ins(T)₁₉ / ins(T)₂₁ / ins(T)₂₂ / ins(T)₂₃
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.06295 (977/15520, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CD247 : Intron Variant
LOC101928512 : 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	15520	TTTTTTTTTTTTTTTTTT=0.91179	TTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00290, TTTTTTTTTTTTTTTTTTTT=0.06295, TTTTTTTTTTTTTTTTTTT=0.01888, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00019, TTTTTTTTTTTTTTTTTTTTT=0.00251, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00077, TTTTTTTTTTTTTTTTTTTTTT=0.00000	0.908086	0.027358	0.064555	32
European	Sub	12200	TTTTTTTTTTTTTTTTTT=0.88795	TTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00369, TTTTTTTTTTTTTTTTTTTT=0.07992, TTTTTTTTTTTTTTTTTTT=0.02402, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00025, TTTTTTTTTTTTTTTTTTTTT=0.00320, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00098, TTTTTTTTTTTTTTTTTTTTTT=0.00000	0.881771	0.035069	0.08316	32
African	Sub	2210	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	90	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	2120	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	58	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	44	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	128	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	462	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	72	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	390	TTTTTTTTTTTTTTTTTT=0.995	TTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.005, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	0.994872	0.005128	0.0	32

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	15520	(T)₁₈=0.91179	del(T)₁₁=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, delTT=0.00000, delT=0.00290, dupT=0.01888, dupTT=0.06295, dupTTT=0.00251, dup(T)₄=0.00000, dup(T)₈=0.00077, dup(T)₁₈=0.00019
Allele Frequency Aggregator	European	Sub	12200	(T)₁₈=0.88795	del(T)₁₁=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, delTT=0.00000, delT=0.00369, dupT=0.02402, dupTT=0.07992, dupTTT=0.00320, dup(T)₄=0.00000, dup(T)₈=0.00098, dup(T)₁₈=0.00025
Allele Frequency Aggregator	African	Sub	2210	(T)₁₈=1.0000	del(T)₁₁=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₈=0.0000, dup(T)₁₈=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	462	(T)₁₈=1.000	del(T)₁₁=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₈=0.000, dup(T)₁₈=0.000
Allele Frequency Aggregator	Other	Sub	390	(T)₁₈=0.995	del(T)₁₁=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.005, dupTTT=0.000, dup(T)₄=0.000, dup(T)₈=0.000, dup(T)₁₈=0.000
Allele Frequency Aggregator	Latin American 1	Sub	128	(T)₁₈=1.000	del(T)₁₁=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₈=0.000, dup(T)₁₈=0.000
Allele Frequency Aggregator	South Asian	Sub	72	(T)₁₈=1.00	del(T)₁₁=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₈=0.00, dup(T)₁₈=0.00
Allele Frequency Aggregator	Asian	Sub	58	(T)₁₈=1.00	del(T)₁₁=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₈=0.00, dup(T)₁₈=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 1	NC_000001.11:g.167465335_167465345del
GRCh38.p14 chr 1	NC_000001.11:g.167465338_167465345del
GRCh38.p14 chr 1	NC_000001.11:g.167465339_167465345del
GRCh38.p14 chr 1	NC_000001.11:g.167465340_167465345del
GRCh38.p14 chr 1	NC_000001.11:g.167465341_167465345del
GRCh38.p14 chr 1	NC_000001.11:g.167465342_167465345del
GRCh38.p14 chr 1	NC_000001.11:g.167465344_167465345del
GRCh38.p14 chr 1	NC_000001.11:g.167465345del
GRCh38.p14 chr 1	NC_000001.11:g.167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465344_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465343_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465342_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465341_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465340_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465339_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465338_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465337_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465336_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465335_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465330_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465329_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465328_167465345dup
GRCh38.p14 chr 1	NC_000001.11:g.167465345_167465346insTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.167465345_167465346insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.167465345_167465346insTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.167465345_167465346insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.167434572_167434582del
GRCh37.p13 chr 1	NC_000001.10:g.167434575_167434582del
GRCh37.p13 chr 1	NC_000001.10:g.167434576_167434582del
GRCh37.p13 chr 1	NC_000001.10:g.167434577_167434582del
GRCh37.p13 chr 1	NC_000001.10:g.167434578_167434582del
GRCh37.p13 chr 1	NC_000001.10:g.167434579_167434582del
GRCh37.p13 chr 1	NC_000001.10:g.167434581_167434582del
GRCh37.p13 chr 1	NC_000001.10:g.167434582del
GRCh37.p13 chr 1	NC_000001.10:g.167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434581_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434580_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434579_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434578_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434577_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434576_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434575_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434574_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434573_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434572_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434567_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434566_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434565_167434582dup
GRCh37.p13 chr 1	NC_000001.10:g.167434582_167434583insTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.167434582_167434583insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.167434582_167434583insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.167434582_167434583insTTTTTTTTTTTTTTTTTTTTTTT
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58272_58282del
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58275_58282del
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58276_58282del
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58277_58282del
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58278_58282del
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58279_58282del
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58281_58282del
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58282del
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58281_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58280_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58279_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58278_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58277_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58276_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58275_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58274_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58273_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58272_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58267_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58266_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58265_58282dup
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58282_58283insAAAAAAAAAAAAAAAAAAA
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58282_58283insAAAAAAAAAAAAAAAAAAAAA
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58282_58283insAAAAAAAAAAAAAAAAAAAAAA
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58282_58283insAAAAAAAAAAAAAAAAAAAAAAA

Gene: CD247, CD247 molecule (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CD247 transcript variant 2	NM_000734.4:c.59-24571_59… NM_000734.4:c.59-24571_59-24561del	N/A	Intron Variant
CD247 transcript variant 3	NM_001378515.1:c.152-2457… NM_001378515.1:c.152-24571_152-24561del	N/A	Intron Variant
CD247 transcript variant 4	NM_001378516.1:c.152-2457… NM_001378516.1:c.152-24571_152-24561del	N/A	Intron Variant
CD247 transcript variant 1	NM_198053.3:c.59-24571_59… NM_198053.3:c.59-24571_59-24561del	N/A	Intron Variant
CD247 transcript variant X1	XM_011510144.3:c.-63-1685… XM_011510144.3:c.-63-16851_-63-16841del	N/A	Intron Variant
CD247 transcript variant X2	XM_011510145.2:c.-63-1685… XM_011510145.2:c.-63-16851_-63-16841del	N/A	Intron Variant

Gene: LOC101928512, uncharacterized LOC101928512 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC101928512 transcript variant X8	XR_007066724.1:n.	N/A	Intron Variant
LOC101928512 transcript variant X4	XR_002958381.2:n.	N/A	Genic Downstream Transcript Variant
LOC101928512 transcript variant X1	XR_002958382.2:n.	N/A	Genic Downstream Transcript Variant
LOC101928512 transcript variant X2	XR_007066719.1:n.	N/A	Genic Downstream Transcript Variant
LOC101928512 transcript variant X3	XR_007066720.1:n.	N/A	Genic Downstream Transcript Variant
LOC101928512 transcript variant X5	XR_007066721.1:n.	N/A	Genic Downstream Transcript Variant
LOC101928512 transcript variant X6	XR_007066722.1:n.	N/A	Genic Downstream Transcript Variant
LOC101928512 transcript variant X7	XR_007066723.1:n.	N/A	Genic Downstream 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)₁₈=	del(T)₁₁	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	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	dup(T)₁₁	dup(T)₁₆	dup(T)₁₇	dup(T)₁₈	ins(T)₁₉	ins(T)₂₁	ins(T)₂₂	ins(T)₂₃
GRCh38.p14 chr 1	NC_000001.11:g.167465328_167465345=	NC_000001.11:g.167465335_167465345del	NC_000001.11:g.167465338_167465345del	NC_000001.11:g.167465339_167465345del	NC_000001.11:g.167465340_167465345del	NC_000001.11:g.167465341_167465345del	NC_000001.11:g.167465342_167465345del	NC_000001.11:g.167465344_167465345del	NC_000001.11:g.167465345del	NC_000001.11:g.167465345dup	NC_000001.11:g.167465344_167465345dup	NC_000001.11:g.167465343_167465345dup	NC_000001.11:g.167465342_167465345dup	NC_000001.11:g.167465341_167465345dup	NC_000001.11:g.167465340_167465345dup	NC_000001.11:g.167465339_167465345dup	NC_000001.11:g.167465338_167465345dup	NC_000001.11:g.167465337_167465345dup	NC_000001.11:g.167465336_167465345dup	NC_000001.11:g.167465335_167465345dup	NC_000001.11:g.167465330_167465345dup	NC_000001.11:g.167465329_167465345dup	NC_000001.11:g.167465328_167465345dup	NC_000001.11:g.167465345_167465346insTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.167465345_167465346insTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.167465345_167465346insTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.167465345_167465346insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.167434565_167434582=	NC_000001.10:g.167434572_167434582del	NC_000001.10:g.167434575_167434582del	NC_000001.10:g.167434576_167434582del	NC_000001.10:g.167434577_167434582del	NC_000001.10:g.167434578_167434582del	NC_000001.10:g.167434579_167434582del	NC_000001.10:g.167434581_167434582del	NC_000001.10:g.167434582del	NC_000001.10:g.167434582dup	NC_000001.10:g.167434581_167434582dup	NC_000001.10:g.167434580_167434582dup	NC_000001.10:g.167434579_167434582dup	NC_000001.10:g.167434578_167434582dup	NC_000001.10:g.167434577_167434582dup	NC_000001.10:g.167434576_167434582dup	NC_000001.10:g.167434575_167434582dup	NC_000001.10:g.167434574_167434582dup	NC_000001.10:g.167434573_167434582dup	NC_000001.10:g.167434572_167434582dup	NC_000001.10:g.167434567_167434582dup	NC_000001.10:g.167434566_167434582dup	NC_000001.10:g.167434565_167434582dup	NC_000001.10:g.167434582_167434583insTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.167434582_167434583insTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.167434582_167434583insTTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.167434582_167434583insTTTTTTTTTTTTTTTTTTTTTTT
CD247 RefSeqGene (LRG_36)	NG_007384.1:g.58265_58282=	NG_007384.1:g.58272_58282del	NG_007384.1:g.58275_58282del	NG_007384.1:g.58276_58282del	NG_007384.1:g.58277_58282del	NG_007384.1:g.58278_58282del	NG_007384.1:g.58279_58282del	NG_007384.1:g.58281_58282del	NG_007384.1:g.58282del	NG_007384.1:g.58282dup	NG_007384.1:g.58281_58282dup	NG_007384.1:g.58280_58282dup	NG_007384.1:g.58279_58282dup	NG_007384.1:g.58278_58282dup	NG_007384.1:g.58277_58282dup	NG_007384.1:g.58276_58282dup	NG_007384.1:g.58275_58282dup	NG_007384.1:g.58274_58282dup	NG_007384.1:g.58273_58282dup	NG_007384.1:g.58272_58282dup	NG_007384.1:g.58267_58282dup	NG_007384.1:g.58266_58282dup	NG_007384.1:g.58265_58282dup	NG_007384.1:g.58282_58283insAAAAAAAAAAAAAAAAAAA	NG_007384.1:g.58282_58283insAAAAAAAAAAAAAAAAAAAAA	NG_007384.1:g.58282_58283insAAAAAAAAAAAAAAAAAAAAAA	NG_007384.1:g.58282_58283insAAAAAAAAAAAAAAAAAAAAAAA
CD247 transcript variant 2	NM_000734.3:c.59-24561=	NM_000734.3:c.59-24571_59-24561del	NM_000734.3:c.59-24568_59-24561del	NM_000734.3:c.59-24567_59-24561del	NM_000734.3:c.59-24566_59-24561del	NM_000734.3:c.59-24565_59-24561del	NM_000734.3:c.59-24564_59-24561del	NM_000734.3:c.59-24562_59-24561del	NM_000734.3:c.59-24561del	NM_000734.3:c.59-24561dup	NM_000734.3:c.59-24562_59-24561dup	NM_000734.3:c.59-24563_59-24561dup	NM_000734.3:c.59-24564_59-24561dup	NM_000734.3:c.59-24565_59-24561dup	NM_000734.3:c.59-24566_59-24561dup	NM_000734.3:c.59-24567_59-24561dup	NM_000734.3:c.59-24568_59-24561dup	NM_000734.3:c.59-24569_59-24561dup	NM_000734.3:c.59-24570_59-24561dup	NM_000734.3:c.59-24571_59-24561dup	NM_000734.3:c.59-24576_59-24561dup	NM_000734.3:c.59-24577_59-24561dup	NM_000734.3:c.59-24578_59-24561dup	NM_000734.3:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAA	NM_000734.3:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAA	NM_000734.3:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAAA	NM_000734.3:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAAAA
CD247 transcript variant 2	NM_000734.4:c.59-24561=	NM_000734.4:c.59-24571_59-24561del	NM_000734.4:c.59-24568_59-24561del	NM_000734.4:c.59-24567_59-24561del	NM_000734.4:c.59-24566_59-24561del	NM_000734.4:c.59-24565_59-24561del	NM_000734.4:c.59-24564_59-24561del	NM_000734.4:c.59-24562_59-24561del	NM_000734.4:c.59-24561del	NM_000734.4:c.59-24561dup	NM_000734.4:c.59-24562_59-24561dup	NM_000734.4:c.59-24563_59-24561dup	NM_000734.4:c.59-24564_59-24561dup	NM_000734.4:c.59-24565_59-24561dup	NM_000734.4:c.59-24566_59-24561dup	NM_000734.4:c.59-24567_59-24561dup	NM_000734.4:c.59-24568_59-24561dup	NM_000734.4:c.59-24569_59-24561dup	NM_000734.4:c.59-24570_59-24561dup	NM_000734.4:c.59-24571_59-24561dup	NM_000734.4:c.59-24576_59-24561dup	NM_000734.4:c.59-24577_59-24561dup	NM_000734.4:c.59-24578_59-24561dup	NM_000734.4:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAA	NM_000734.4:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAA	NM_000734.4:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAAA	NM_000734.4:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAAAA
CD247 transcript variant 3	NM_001378515.1:c.152-24561=	NM_001378515.1:c.152-24571_152-24561del	NM_001378515.1:c.152-24568_152-24561del	NM_001378515.1:c.152-24567_152-24561del	NM_001378515.1:c.152-24566_152-24561del	NM_001378515.1:c.152-24565_152-24561del	NM_001378515.1:c.152-24564_152-24561del	NM_001378515.1:c.152-24562_152-24561del	NM_001378515.1:c.152-24561del	NM_001378515.1:c.152-24561dup	NM_001378515.1:c.152-24562_152-24561dup	NM_001378515.1:c.152-24563_152-24561dup	NM_001378515.1:c.152-24564_152-24561dup	NM_001378515.1:c.152-24565_152-24561dup	NM_001378515.1:c.152-24566_152-24561dup	NM_001378515.1:c.152-24567_152-24561dup	NM_001378515.1:c.152-24568_152-24561dup	NM_001378515.1:c.152-24569_152-24561dup	NM_001378515.1:c.152-24570_152-24561dup	NM_001378515.1:c.152-24571_152-24561dup	NM_001378515.1:c.152-24576_152-24561dup	NM_001378515.1:c.152-24577_152-24561dup	NM_001378515.1:c.152-24578_152-24561dup	NM_001378515.1:c.152-24561_152-24560insAAAAAAAAAAAAAAAAAAA	NM_001378515.1:c.152-24561_152-24560insAAAAAAAAAAAAAAAAAAAAA	NM_001378515.1:c.152-24561_152-24560insAAAAAAAAAAAAAAAAAAAAAA	NM_001378515.1:c.152-24561_152-24560insAAAAAAAAAAAAAAAAAAAAAAA
CD247 transcript variant 4	NM_001378516.1:c.152-24561=	NM_001378516.1:c.152-24571_152-24561del	NM_001378516.1:c.152-24568_152-24561del	NM_001378516.1:c.152-24567_152-24561del	NM_001378516.1:c.152-24566_152-24561del	NM_001378516.1:c.152-24565_152-24561del	NM_001378516.1:c.152-24564_152-24561del	NM_001378516.1:c.152-24562_152-24561del	NM_001378516.1:c.152-24561del	NM_001378516.1:c.152-24561dup	NM_001378516.1:c.152-24562_152-24561dup	NM_001378516.1:c.152-24563_152-24561dup	NM_001378516.1:c.152-24564_152-24561dup	NM_001378516.1:c.152-24565_152-24561dup	NM_001378516.1:c.152-24566_152-24561dup	NM_001378516.1:c.152-24567_152-24561dup	NM_001378516.1:c.152-24568_152-24561dup	NM_001378516.1:c.152-24569_152-24561dup	NM_001378516.1:c.152-24570_152-24561dup	NM_001378516.1:c.152-24571_152-24561dup	NM_001378516.1:c.152-24576_152-24561dup	NM_001378516.1:c.152-24577_152-24561dup	NM_001378516.1:c.152-24578_152-24561dup	NM_001378516.1:c.152-24561_152-24560insAAAAAAAAAAAAAAAAAAA	NM_001378516.1:c.152-24561_152-24560insAAAAAAAAAAAAAAAAAAAAA	NM_001378516.1:c.152-24561_152-24560insAAAAAAAAAAAAAAAAAAAAAA	NM_001378516.1:c.152-24561_152-24560insAAAAAAAAAAAAAAAAAAAAAAA
CD247 transcript variant 1	NM_198053.2:c.59-24561=	NM_198053.2:c.59-24571_59-24561del	NM_198053.2:c.59-24568_59-24561del	NM_198053.2:c.59-24567_59-24561del	NM_198053.2:c.59-24566_59-24561del	NM_198053.2:c.59-24565_59-24561del	NM_198053.2:c.59-24564_59-24561del	NM_198053.2:c.59-24562_59-24561del	NM_198053.2:c.59-24561del	NM_198053.2:c.59-24561dup	NM_198053.2:c.59-24562_59-24561dup	NM_198053.2:c.59-24563_59-24561dup	NM_198053.2:c.59-24564_59-24561dup	NM_198053.2:c.59-24565_59-24561dup	NM_198053.2:c.59-24566_59-24561dup	NM_198053.2:c.59-24567_59-24561dup	NM_198053.2:c.59-24568_59-24561dup	NM_198053.2:c.59-24569_59-24561dup	NM_198053.2:c.59-24570_59-24561dup	NM_198053.2:c.59-24571_59-24561dup	NM_198053.2:c.59-24576_59-24561dup	NM_198053.2:c.59-24577_59-24561dup	NM_198053.2:c.59-24578_59-24561dup	NM_198053.2:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAA	NM_198053.2:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAA	NM_198053.2:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAAA	NM_198053.2:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAAAA
CD247 transcript variant 1	NM_198053.3:c.59-24561=	NM_198053.3:c.59-24571_59-24561del	NM_198053.3:c.59-24568_59-24561del	NM_198053.3:c.59-24567_59-24561del	NM_198053.3:c.59-24566_59-24561del	NM_198053.3:c.59-24565_59-24561del	NM_198053.3:c.59-24564_59-24561del	NM_198053.3:c.59-24562_59-24561del	NM_198053.3:c.59-24561del	NM_198053.3:c.59-24561dup	NM_198053.3:c.59-24562_59-24561dup	NM_198053.3:c.59-24563_59-24561dup	NM_198053.3:c.59-24564_59-24561dup	NM_198053.3:c.59-24565_59-24561dup	NM_198053.3:c.59-24566_59-24561dup	NM_198053.3:c.59-24567_59-24561dup	NM_198053.3:c.59-24568_59-24561dup	NM_198053.3:c.59-24569_59-24561dup	NM_198053.3:c.59-24570_59-24561dup	NM_198053.3:c.59-24571_59-24561dup	NM_198053.3:c.59-24576_59-24561dup	NM_198053.3:c.59-24577_59-24561dup	NM_198053.3:c.59-24578_59-24561dup	NM_198053.3:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAA	NM_198053.3:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAA	NM_198053.3:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAAA	NM_198053.3:c.59-24561_59-24560insAAAAAAAAAAAAAAAAAAAAAAA
CD247 transcript variant X1	XM_005245596.1:c.-63-16841=	XM_005245596.1:c.-63-16851_-63-16841del	XM_005245596.1:c.-63-16848_-63-16841del	XM_005245596.1:c.-63-16847_-63-16841del	XM_005245596.1:c.-63-16846_-63-16841del	XM_005245596.1:c.-63-16845_-63-16841del	XM_005245596.1:c.-63-16844_-63-16841del	XM_005245596.1:c.-63-16842_-63-16841del	XM_005245596.1:c.-63-16841del	XM_005245596.1:c.-63-16841dup	XM_005245596.1:c.-63-16842_-63-16841dup	XM_005245596.1:c.-63-16843_-63-16841dup	XM_005245596.1:c.-63-16844_-63-16841dup	XM_005245596.1:c.-63-16845_-63-16841dup	XM_005245596.1:c.-63-16846_-63-16841dup	XM_005245596.1:c.-63-16847_-63-16841dup	XM_005245596.1:c.-63-16848_-63-16841dup	XM_005245596.1:c.-63-16849_-63-16841dup	XM_005245596.1:c.-63-16850_-63-16841dup	XM_005245596.1:c.-63-16851_-63-16841dup	XM_005245596.1:c.-63-16856_-63-16841dup	XM_005245596.1:c.-63-16857_-63-16841dup	XM_005245596.1:c.-63-16858_-63-16841dup	XM_005245596.1:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAA	XM_005245596.1:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAAAA	XM_005245596.1:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAAAAA	XM_005245596.1:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAAAAAA
CD247 transcript variant X1	XM_011510144.3:c.-63-16841=	XM_011510144.3:c.-63-16851_-63-16841del	XM_011510144.3:c.-63-16848_-63-16841del	XM_011510144.3:c.-63-16847_-63-16841del	XM_011510144.3:c.-63-16846_-63-16841del	XM_011510144.3:c.-63-16845_-63-16841del	XM_011510144.3:c.-63-16844_-63-16841del	XM_011510144.3:c.-63-16842_-63-16841del	XM_011510144.3:c.-63-16841del	XM_011510144.3:c.-63-16841dup	XM_011510144.3:c.-63-16842_-63-16841dup	XM_011510144.3:c.-63-16843_-63-16841dup	XM_011510144.3:c.-63-16844_-63-16841dup	XM_011510144.3:c.-63-16845_-63-16841dup	XM_011510144.3:c.-63-16846_-63-16841dup	XM_011510144.3:c.-63-16847_-63-16841dup	XM_011510144.3:c.-63-16848_-63-16841dup	XM_011510144.3:c.-63-16849_-63-16841dup	XM_011510144.3:c.-63-16850_-63-16841dup	XM_011510144.3:c.-63-16851_-63-16841dup	XM_011510144.3:c.-63-16856_-63-16841dup	XM_011510144.3:c.-63-16857_-63-16841dup	XM_011510144.3:c.-63-16858_-63-16841dup	XM_011510144.3:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAA	XM_011510144.3:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAAAA	XM_011510144.3:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAAAAA	XM_011510144.3:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAAAAAA
CD247 transcript variant X2	XM_011510145.2:c.-63-16841=	XM_011510145.2:c.-63-16851_-63-16841del	XM_011510145.2:c.-63-16848_-63-16841del	XM_011510145.2:c.-63-16847_-63-16841del	XM_011510145.2:c.-63-16846_-63-16841del	XM_011510145.2:c.-63-16845_-63-16841del	XM_011510145.2:c.-63-16844_-63-16841del	XM_011510145.2:c.-63-16842_-63-16841del	XM_011510145.2:c.-63-16841del	XM_011510145.2:c.-63-16841dup	XM_011510145.2:c.-63-16842_-63-16841dup	XM_011510145.2:c.-63-16843_-63-16841dup	XM_011510145.2:c.-63-16844_-63-16841dup	XM_011510145.2:c.-63-16845_-63-16841dup	XM_011510145.2:c.-63-16846_-63-16841dup	XM_011510145.2:c.-63-16847_-63-16841dup	XM_011510145.2:c.-63-16848_-63-16841dup	XM_011510145.2:c.-63-16849_-63-16841dup	XM_011510145.2:c.-63-16850_-63-16841dup	XM_011510145.2:c.-63-16851_-63-16841dup	XM_011510145.2:c.-63-16856_-63-16841dup	XM_011510145.2:c.-63-16857_-63-16841dup	XM_011510145.2:c.-63-16858_-63-16841dup	XM_011510145.2:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAA	XM_011510145.2:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAAAA	XM_011510145.2:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAAAAA	XM_011510145.2:c.-63-16841_-63-16840insAAAAAAAAAAAAAAAAAAAAAAA

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, 41 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95245915	Oct 11, 2018 (152)
2	PJP	ss294609226	Oct 11, 2018 (152)
3	PJP	ss294609227	Oct 11, 2018 (152)
4	SSMP	ss663129545	Apr 01, 2015 (144)
5	SWEGEN	ss2987899518	Nov 08, 2017 (151)
6	URBANLAB	ss3646811997	Oct 11, 2018 (152)
7	EVA_DECODE	ss3687960377	Jul 12, 2019 (153)
8	EVA_DECODE	ss3687960378	Jul 12, 2019 (153)
9	EVA_DECODE	ss3687960379	Jul 12, 2019 (153)
10	EVA_DECODE	ss3687960380	Jul 12, 2019 (153)
11	EVA_DECODE	ss3687960381	Jul 12, 2019 (153)
12	PACBIO	ss3783592695	Jul 12, 2019 (153)
13	PACBIO	ss3789220081	Jul 12, 2019 (153)
14	PACBIO	ss3789220082	Jul 12, 2019 (153)
15	PACBIO	ss3794092100	Jul 12, 2019 (153)
16	PACBIO	ss3794092101	Jul 12, 2019 (153)
17	KOGIC	ss3945834457	Apr 25, 2020 (154)
18	KOGIC	ss3945834458	Apr 25, 2020 (154)
19	KOGIC	ss3945834459	Apr 25, 2020 (154)
20	KOGIC	ss3945834460	Apr 25, 2020 (154)
21	GNOMAD	ss4005292124	Apr 25, 2021 (155)
22	GNOMAD	ss4005292125	Apr 25, 2021 (155)
23	GNOMAD	ss4005292126	Apr 25, 2021 (155)
24	GNOMAD	ss4005292127	Apr 25, 2021 (155)
25	GNOMAD	ss4005292129	Apr 25, 2021 (155)
26	GNOMAD	ss4005292132	Apr 25, 2021 (155)
27	GNOMAD	ss4005292133	Apr 25, 2021 (155)
28	GNOMAD	ss4005292134	Apr 25, 2021 (155)
29	GNOMAD	ss4005292135	Apr 25, 2021 (155)
30	GNOMAD	ss4005292136	Apr 25, 2021 (155)
31	GNOMAD	ss4005292137	Apr 25, 2021 (155)
32	GNOMAD	ss4005292138	Apr 25, 2021 (155)
33	GNOMAD	ss4005292139	Apr 25, 2021 (155)
34	GNOMAD	ss4005292140	Apr 25, 2021 (155)
35	GNOMAD	ss4005292141	Apr 25, 2021 (155)
36	GNOMAD	ss4005292142	Apr 25, 2021 (155)
37	GNOMAD	ss4005292143	Apr 25, 2021 (155)
38	GNOMAD	ss4005292144	Apr 25, 2021 (155)
39	GNOMAD	ss4005292146	Apr 25, 2021 (155)
40	GNOMAD	ss4005292147	Apr 25, 2021 (155)
41	GNOMAD	ss4005292148	Apr 25, 2021 (155)
42	GNOMAD	ss4005292149	Apr 25, 2021 (155)
43	GNOMAD	ss4005292150	Apr 25, 2021 (155)
44	GNOMAD	ss4005292151	Apr 25, 2021 (155)
45	GNOMAD	ss4005292152	Apr 25, 2021 (155)
46	GNOMAD	ss4005292153	Apr 25, 2021 (155)
47	TOPMED	ss4471474701	Apr 25, 2021 (155)
48	TOPMED	ss4471474702	Apr 25, 2021 (155)
49	TOMMO_GENOMICS	ss5146894864	Apr 25, 2021 (155)
50	TOMMO_GENOMICS	ss5146894865	Apr 25, 2021 (155)
51	TOMMO_GENOMICS	ss5146894867	Apr 25, 2021 (155)
52	TOMMO_GENOMICS	ss5146894868	Apr 25, 2021 (155)
53	1000G_HIGH_COVERAGE	ss5244607890	Oct 12, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5244607891	Oct 12, 2022 (156)
55	HUGCELL_USP	ss5445160291	Oct 12, 2022 (156)
56	HUGCELL_USP	ss5445160292	Oct 12, 2022 (156)
57	HUGCELL_USP	ss5445160293	Oct 12, 2022 (156)
58	HUGCELL_USP	ss5445160294	Oct 12, 2022 (156)
59	TOMMO_GENOMICS	ss5674212727	Oct 12, 2022 (156)
60	TOMMO_GENOMICS	ss5674212728	Oct 12, 2022 (156)
61	TOMMO_GENOMICS	ss5674212731	Oct 12, 2022 (156)
62	TOMMO_GENOMICS	ss5674212732	Oct 12, 2022 (156)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 29656456 (NC_000001.11:167465327::T 10061/106398) Row 29656457 (NC_000001.11:167465327::TT 26842/106400) Row 29656458 (NC_000001.11:167465327::TTT 1103/106440)...	-	Apr 25, 2021 (155)
89	Korean Genome Project Submission ignored due to conflicting rows: Row 2212458 (NC_000001.11:167465328::T 406/1824) Row 2212459 (NC_000001.11:167465328::TT 141/1824) Row 2212460 (NC_000001.11:167465328::TTT 27/1824)...	-	Apr 25, 2020 (154)
90	Korean Genome Project Submission ignored due to conflicting rows: Row 2212458 (NC_000001.11:167465328::T 406/1824) Row 2212459 (NC_000001.11:167465328::TT 141/1824) Row 2212460 (NC_000001.11:167465328::TTT 27/1824)...	-	Apr 25, 2020 (154)
91	Korean Genome Project Submission ignored due to conflicting rows: Row 2212458 (NC_000001.11:167465328::T 406/1824) Row 2212459 (NC_000001.11:167465328::TT 141/1824) Row 2212460 (NC_000001.11:167465328::TTT 27/1824)...	-	Apr 25, 2020 (154)
92	Korean Genome Project Submission ignored due to conflicting rows: Row 2212458 (NC_000001.11:167465328::T 406/1824) Row 2212459 (NC_000001.11:167465328::TT 141/1824) Row 2212460 (NC_000001.11:167465328::TTT 27/1824)...	-	Apr 25, 2020 (154)
93	8.3KJPN Submission ignored due to conflicting rows: Row 4864171 (NC_000001.10:167434564::T 3680/16660) Row 4864172 (NC_000001.10:167434564::TT 806/16660) Row 4864174 (NC_000001.10:167434564::TTTTTTTT 8/16660)...	-	Apr 25, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 4864171 (NC_000001.10:167434564::T 3680/16660) Row 4864172 (NC_000001.10:167434564::TT 806/16660) Row 4864174 (NC_000001.10:167434564::TTTTTTTT 8/16660)...	-	Apr 25, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 4864171 (NC_000001.10:167434564::T 3680/16660) Row 4864172 (NC_000001.10:167434564::TT 806/16660) Row 4864174 (NC_000001.10:167434564::TTTTTTTT 8/16660)...	-	Apr 25, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 4864171 (NC_000001.10:167434564::T 3680/16660) Row 4864172 (NC_000001.10:167434564::TT 806/16660) Row 4864174 (NC_000001.10:167434564::TTTTTTTT 8/16660)...	-	Apr 25, 2021 (155)
97	14KJPN Submission ignored due to conflicting rows: Row 8049831 (NC_000001.11:167465327::TT 1185/24484) Row 8049832 (NC_000001.11:167465327::T 5118/24484) Row 8049835 (NC_000001.11:167465327::TTT 3/24484)...	-	Oct 12, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 8049831 (NC_000001.11:167465327::TT 1185/24484) Row 8049832 (NC_000001.11:167465327::T 5118/24484) Row 8049835 (NC_000001.11:167465327::TTT 3/24484)...	-	Oct 12, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 8049831 (NC_000001.11:167465327::TT 1185/24484) Row 8049832 (NC_000001.11:167465327::T 5118/24484) Row 8049835 (NC_000001.11:167465327::TTT 3/24484)...	-	Oct 12, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 8049831 (NC_000001.11:167465327::TT 1185/24484) Row 8049832 (NC_000001.11:167465327::T 5118/24484) Row 8049835 (NC_000001.11:167465327::TTT 3/24484)...	-	Oct 12, 2022 (156)
101	TopMed Submission ignored due to conflicting rows: Row 35081036 (NC_000001.11:167465327:TTTTTT: 1/264690) Row 35081037 (NC_000001.11:167465327:TTTTTTTT: 3/264690)	-	Apr 25, 2021 (155)
102	TopMed Submission ignored due to conflicting rows: Row 35081036 (NC_000001.11:167465327:TTTTTT: 1/264690) Row 35081037 (NC_000001.11:167465327:TTTTTTTT: 3/264690)	-	Apr 25, 2021 (155)
103	ALFA	NC_000001.11 - 167465328	Apr 25, 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
ss4005292153	NC_000001.11:167465327:TTTTTTTTTTT:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTT	(self)
ss4005292152, ss4471474702	NC_000001.11:167465327:TTTTTTTT:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4005292151	NC_000001.11:167465327:TTTTTTT:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4005292150, ss4471474701	NC_000001.11:167465327:TTTTTT:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4005292149	NC_000001.11:167465327:TTTTT:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4005292148	NC_000001.11:167465327:TTTT:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3687960377, ss4005292147	NC_000001.11:167465327:TT:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss2987899518	NC_000001.10:167434564:T:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3945834460, ss4005292146, ss5244607891, ss5445160293, ss5674212732	NC_000001.11:167465327:T:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3687960378	NC_000001.11:167465328:T:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss294609226	NC_000001.9:165701189::T	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss663129545, ss3783592695, ss3789220081, ss3794092100, ss5146894864	NC_000001.10:167434564::T	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4005292124, ss5445160291, ss5674212728	NC_000001.11:167465327::T	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3945834457	NC_000001.11:167465328::T	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3687960379	NC_000001.11:167465329::T	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss294609227	NC_000001.9:165701205::TT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3789220082, ss3794092101, ss5146894865	NC_000001.10:167434564::TT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3646811997, ss4005292125, ss5244607890, ss5445160292, ss5674212727	NC_000001.11:167465327::TT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3945834458	NC_000001.11:167465328::TT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3687960380	NC_000001.11:167465329::TT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss95245915	NT_004487.19:18923224::TT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4005292126, ss5445160294, ss5674212731	NC_000001.11:167465327::TTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3945834459	NC_000001.11:167465328::TTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3687960381	NC_000001.11:167465329::TTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292127	NC_000001.11:167465327::TTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292129	NC_000001.11:167465327::TTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292132	NC_000001.11:167465327::TTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5146894868	NC_000001.10:167434564::TTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292133	NC_000001.11:167465327::TTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5146894867	NC_000001.10:167434564::TTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292134	NC_000001.11:167465327::TTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292135	NC_000001.11:167465327::TTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292136	NC_000001.11:167465327::TTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292137	NC_000001.11:167465327::TTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292138	NC_000001.11:167465327::TTTTTTTTTT… NC_000001.11:167465327::TTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292139	NC_000001.11:167465327::TTTTTTTTTT… NC_000001.11:167465327::TTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292140	NC_000001.11:167465327::TTTTTTTTTT… NC_000001.11:167465327::TTTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3171923070	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292141	NC_000001.11:167465327::TTTTTTTTTT… NC_000001.11:167465327::TTTTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292142	NC_000001.11:167465327::TTTTTTTTTT… NC_000001.11:167465327::TTTTTTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292143	NC_000001.11:167465327::TTTTTTTTTT… NC_000001.11:167465327::TTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4005292144	NC_000001.11:167465327::TTTTTTTTTT… NC_000001.11:167465327::TTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2329804299	NC_000001.10:167434564:TTTTTTT:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT
ss2329804300	NC_000001.10:167434564:TTTTTTTT:	NC_000001.11:167465327:TTTTTTTTTTT… NC_000001.11:167465327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT

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

No publications for rs765176193

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

rs765176193