Name: rs1354151315
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.

rs1354151315

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:40880797-40880799 (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: delGG / insGC(G)₈ / dupGG / insGGC…
delGG / insGC(G)₈ / dupGG / insGGC(G)₇ / dupGGG / insGGGC(G)₆ / ins(G)₄ / ins(G)₅C(G)₄ / ins(G)₆ / ins(G)₇ / ins(G)₈ / ins(G)₉ / ins(G)₁₀ / ins(G)₁₁ / ins(G)₁₂ / ins(G)₁₃ / ins(G)₁₄ / ins(G)₁₅ / ins(G)₁₇ / ins(G)₁₈ / ins(G)₅T(G)₄ / insGGT(G)₆ / insGGT(G)₇ / insTT(G)₇
Variation Type: Indel Insertion and Deletion
Frequency: delGG=0.00000 (0/11760, ALFA)
insGC(G)₈=0.00000 (0/11760, ALFA)
dupGG=0.00000 (0/11760, ALFA) (+ 20 more)
insGGC(G)₇=0.00000 (0/11760, ALFA)
dupGGG=0.00000 (0/11760, ALFA)
insGGGC(G)₆=0.00000 (0/11760, ALFA)
ins(G)₄=0.00000 (0/11760, ALFA)
ins(G)₅C(G)₄=0.00000 (0/11760, ALFA)
ins(G)₆=0.00000 (0/11760, ALFA)
ins(G)₇=0.00000 (0/11760, ALFA)
ins(G)₈=0.00000 (0/11760, ALFA)
ins(G)₉=0.00000 (0/11760, ALFA)
ins(G)₁₀=0.00000 (0/11760, ALFA)
ins(G)₁₁=0.00000 (0/11760, ALFA)
ins(G)₁₂=0.00000 (0/11760, ALFA)
ins(G)₁₃=0.00000 (0/11760, ALFA)
ins(G)₁₄=0.00000 (0/11760, ALFA)
ins(G)₁₅=0.00000 (0/11760, ALFA)
ins(G)₅T(G)₄=0.00000 (0/11760, ALFA)
insGGT(G)₆=0.00000 (0/11760, ALFA)
insGGT(G)₇=0.00000 (0/11760, ALFA)
insTT(G)₇=0.00000 (0/11760, ALFA)
delGG=0.005 (5/986, Korea1K)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CYP2A7 : 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	HWEP
Total	Global	11760	GGG=1.00000	G=0.00000, GGGGCGGGGGGGG=0.00000, GGGGG=0.00000, GGGGGCGGGGGGG=0.00000, GGGGGG=0.00000, GGGGGGCGGGGGG=0.00000, GGGGGGG=0.00000, GGGGGGGGCGGGG=0.00000, GGGGGGGGG=0.00000, GGGGGGGGGG=0.00000, GGGGGGGGGGG=0.00000, GGGGGGGGGGGG=0.00000, GGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGGGG=0.00000, GGGGGGGGGGGGGGGGGG=0.00000, GGGGGGGGTGGGG=0.00000, GGGGGTGGGGGG=0.00000, GGGGGTGGGGGGG=0.00000, GGGTTGGGGGGG=0.00000	1.0	N/A
European	Sub	7552	GGG=1.0000	G=0.0000, GGGGCGGGGGGGG=0.0000, GGGGG=0.0000, GGGGGCGGGGGGG=0.0000, GGGGGG=0.0000, GGGGGGCGGGGGG=0.0000, GGGGGGG=0.0000, GGGGGGGGCGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGTGGGG=0.0000, GGGGGTGGGGGG=0.0000, GGGGGTGGGGGGG=0.0000, GGGTTGGGGGGG=0.0000	1.0	N/A
African	Sub	2786	GGG=1.0000	G=0.0000, GGGGCGGGGGGGG=0.0000, GGGGG=0.0000, GGGGGCGGGGGGG=0.0000, GGGGGG=0.0000, GGGGGGCGGGGGG=0.0000, GGGGGGG=0.0000, GGGGGGGGCGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGTGGGG=0.0000, GGGGGTGGGGGG=0.0000, GGGGGTGGGGGGG=0.0000, GGGTTGGGGGGG=0.0000	1.0	N/A
African Others	Sub	108	GGG=1.000	G=0.000, GGGGCGGGGGGGG=0.000, GGGGG=0.000, GGGGGCGGGGGGG=0.000, GGGGGG=0.000, GGGGGGCGGGGGG=0.000, GGGGGGG=0.000, GGGGGGGGCGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGTGGGG=0.000, GGGGGTGGGGGG=0.000, GGGGGTGGGGGGG=0.000, GGGTTGGGGGGG=0.000	1.0	N/A
African American	Sub	2678	GGG=1.0000	G=0.0000, GGGGCGGGGGGGG=0.0000, GGGGG=0.0000, GGGGGCGGGGGGG=0.0000, GGGGGG=0.0000, GGGGGGCGGGGGG=0.0000, GGGGGGG=0.0000, GGGGGGGGCGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGTGGGG=0.0000, GGGGGTGGGGGG=0.0000, GGGGGTGGGGGGG=0.0000, GGGTTGGGGGGG=0.0000	1.0	N/A
Asian	Sub	108	GGG=1.000	G=0.000, GGGGCGGGGGGGG=0.000, GGGGG=0.000, GGGGGCGGGGGGG=0.000, GGGGGG=0.000, GGGGGGCGGGGGG=0.000, GGGGGGG=0.000, GGGGGGGGCGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGTGGGG=0.000, GGGGGTGGGGGG=0.000, GGGGGTGGGGGGG=0.000, GGGTTGGGGGGG=0.000	1.0	N/A
East Asian	Sub	84	GGG=1.00	G=0.00, GGGGCGGGGGGGG=0.00, GGGGG=0.00, GGGGGCGGGGGGG=0.00, GGGGGG=0.00, GGGGGGCGGGGGG=0.00, GGGGGGG=0.00, GGGGGGGGCGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGTGGGG=0.00, GGGGGTGGGGGG=0.00, GGGGGTGGGGGGG=0.00, GGGTTGGGGGGG=0.00	1.0	N/A
Other Asian	Sub	24	GGG=1.00	G=0.00, GGGGCGGGGGGGG=0.00, GGGGG=0.00, GGGGGCGGGGGGG=0.00, GGGGGG=0.00, GGGGGGCGGGGGG=0.00, GGGGGGG=0.00, GGGGGGGGCGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGTGGGG=0.00, GGGGGTGGGGGG=0.00, GGGGGTGGGGGGG=0.00, GGGTTGGGGGGG=0.00	1.0	N/A
Latin American 1	Sub	146	GGG=1.000	G=0.000, GGGGCGGGGGGGG=0.000, GGGGG=0.000, GGGGGCGGGGGGG=0.000, GGGGGG=0.000, GGGGGGCGGGGGG=0.000, GGGGGGG=0.000, GGGGGGGGCGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGTGGGG=0.000, GGGGGTGGGGGG=0.000, GGGGGTGGGGGGG=0.000, GGGTTGGGGGGG=0.000	1.0	N/A
Latin American 2	Sub	608	GGG=1.000	G=0.000, GGGGCGGGGGGGG=0.000, GGGGG=0.000, GGGGGCGGGGGGG=0.000, GGGGGG=0.000, GGGGGGCGGGGGG=0.000, GGGGGGG=0.000, GGGGGGGGCGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGTGGGG=0.000, GGGGGTGGGGGG=0.000, GGGGGTGGGGGGG=0.000, GGGTTGGGGGGG=0.000	1.0	N/A
South Asian	Sub	92	GGG=1.00	G=0.00, GGGGCGGGGGGGG=0.00, GGGGG=0.00, GGGGGCGGGGGGG=0.00, GGGGGG=0.00, GGGGGGCGGGGGG=0.00, GGGGGGG=0.00, GGGGGGGGCGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGTGGGG=0.00, GGGGGTGGGGGG=0.00, GGGGGTGGGGGGG=0.00, GGGTTGGGGGGG=0.00	1.0	N/A
Other	Sub	468	GGG=1.000	G=0.000, GGGGCGGGGGGGG=0.000, GGGGG=0.000, GGGGGCGGGGGGG=0.000, GGGGGG=0.000, GGGGGGCGGGGGG=0.000, GGGGGGG=0.000, GGGGGGGGCGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGTGGGG=0.000, GGGGGTGGGGGG=0.000, GGGGGTGGGGGGG=0.000, GGGTTGGGGGGG=0.000	1.0	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	11760	GGG=1.00000	delGG=0.00000, insGC(G)₈=0.00000, dupGG=0.00000, insGGC(G)₇=0.00000, dupGGG=0.00000, insGGGC(G)₆=0.00000, ins(G)₄=0.00000, ins(G)₅C(G)₄=0.00000, ins(G)₆=0.00000, ins(G)₇=0.00000, ins(G)₈=0.00000, ins(G)₉=0.00000, ins(G)₁₀=0.00000, ins(G)₁₁=0.00000, ins(G)₁₂=0.00000, ins(G)₁₃=0.00000, ins(G)₁₄=0.00000, ins(G)₁₅=0.00000, ins(G)₅T(G)₄=0.00000, insGGT(G)₆=0.00000, insGGT(G)₇=0.00000, insTT(G)₇=0.00000
Allele Frequency Aggregator	European	Sub	7552	GGG=1.0000	delGG=0.0000, insGC(G)₈=0.0000, dupGG=0.0000, insGGC(G)₇=0.0000, dupGGG=0.0000, insGGGC(G)₆=0.0000, ins(G)₄=0.0000, ins(G)₅C(G)₄=0.0000, ins(G)₆=0.0000, ins(G)₇=0.0000, ins(G)₈=0.0000, ins(G)₉=0.0000, ins(G)₁₀=0.0000, ins(G)₁₁=0.0000, ins(G)₁₂=0.0000, ins(G)₁₃=0.0000, ins(G)₁₄=0.0000, ins(G)₁₅=0.0000, ins(G)₅T(G)₄=0.0000, insGGT(G)₆=0.0000, insGGT(G)₇=0.0000, insTT(G)₇=0.0000
Allele Frequency Aggregator	African	Sub	2786	GGG=1.0000	delGG=0.0000, insGC(G)₈=0.0000, dupGG=0.0000, insGGC(G)₇=0.0000, dupGGG=0.0000, insGGGC(G)₆=0.0000, ins(G)₄=0.0000, ins(G)₅C(G)₄=0.0000, ins(G)₆=0.0000, ins(G)₇=0.0000, ins(G)₈=0.0000, ins(G)₉=0.0000, ins(G)₁₀=0.0000, ins(G)₁₁=0.0000, ins(G)₁₂=0.0000, ins(G)₁₃=0.0000, ins(G)₁₄=0.0000, ins(G)₁₅=0.0000, ins(G)₅T(G)₄=0.0000, insGGT(G)₆=0.0000, insGGT(G)₇=0.0000, insTT(G)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	608	GGG=1.000	delGG=0.000, insGC(G)₈=0.000, dupGG=0.000, insGGC(G)₇=0.000, dupGGG=0.000, insGGGC(G)₆=0.000, ins(G)₄=0.000, ins(G)₅C(G)₄=0.000, ins(G)₆=0.000, ins(G)₇=0.000, ins(G)₈=0.000, ins(G)₉=0.000, ins(G)₁₀=0.000, ins(G)₁₁=0.000, ins(G)₁₂=0.000, ins(G)₁₃=0.000, ins(G)₁₄=0.000, ins(G)₁₅=0.000, ins(G)₅T(G)₄=0.000, insGGT(G)₆=0.000, insGGT(G)₇=0.000, insTT(G)₇=0.000
Allele Frequency Aggregator	Other	Sub	468	GGG=1.000	delGG=0.000, insGC(G)₈=0.000, dupGG=0.000, insGGC(G)₇=0.000, dupGGG=0.000, insGGGC(G)₆=0.000, ins(G)₄=0.000, ins(G)₅C(G)₄=0.000, ins(G)₆=0.000, ins(G)₇=0.000, ins(G)₈=0.000, ins(G)₉=0.000, ins(G)₁₀=0.000, ins(G)₁₁=0.000, ins(G)₁₂=0.000, ins(G)₁₃=0.000, ins(G)₁₄=0.000, ins(G)₁₅=0.000, ins(G)₅T(G)₄=0.000, insGGT(G)₆=0.000, insGGT(G)₇=0.000, insTT(G)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	GGG=1.000	delGG=0.000, insGC(G)₈=0.000, dupGG=0.000, insGGC(G)₇=0.000, dupGGG=0.000, insGGGC(G)₆=0.000, ins(G)₄=0.000, ins(G)₅C(G)₄=0.000, ins(G)₆=0.000, ins(G)₇=0.000, ins(G)₈=0.000, ins(G)₉=0.000, ins(G)₁₀=0.000, ins(G)₁₁=0.000, ins(G)₁₂=0.000, ins(G)₁₃=0.000, ins(G)₁₄=0.000, ins(G)₁₅=0.000, ins(G)₅T(G)₄=0.000, insGGT(G)₆=0.000, insGGT(G)₇=0.000, insTT(G)₇=0.000
Allele Frequency Aggregator	Asian	Sub	108	GGG=1.000	delGG=0.000, insGC(G)₈=0.000, dupGG=0.000, insGGC(G)₇=0.000, dupGGG=0.000, insGGGC(G)₆=0.000, ins(G)₄=0.000, ins(G)₅C(G)₄=0.000, ins(G)₆=0.000, ins(G)₇=0.000, ins(G)₈=0.000, ins(G)₉=0.000, ins(G)₁₀=0.000, ins(G)₁₁=0.000, ins(G)₁₂=0.000, ins(G)₁₃=0.000, ins(G)₁₄=0.000, ins(G)₁₅=0.000, ins(G)₅T(G)₄=0.000, insGGT(G)₆=0.000, insGGT(G)₇=0.000, insTT(G)₇=0.000
Allele Frequency Aggregator	South Asian	Sub	92	GGG=1.00	delGG=0.00, insGC(G)₈=0.00, dupGG=0.00, insGGC(G)₇=0.00, dupGGG=0.00, insGGGC(G)₆=0.00, ins(G)₄=0.00, ins(G)₅C(G)₄=0.00, ins(G)₆=0.00, ins(G)₇=0.00, ins(G)₈=0.00, ins(G)₉=0.00, ins(G)₁₀=0.00, ins(G)₁₁=0.00, ins(G)₁₂=0.00, ins(G)₁₃=0.00, ins(G)₁₄=0.00, ins(G)₁₅=0.00, ins(G)₅T(G)₄=0.00, insGGT(G)₆=0.00, insGGT(G)₇=0.00, insTT(G)₇=0.00
Korean Genome Project	KOREAN	Study-wide	986	GGG=0.995	delGG=0.005

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 19	NC_000019.10:g.40880798_40880799del
GRCh38.p14 chr 19	NC_000019.10:g.40880797_40880799G[4]CGGGGGGGG[1]
GRCh38.p14 chr 19	NC_000019.10:g.40880798_40880799dup
GRCh38.p14 chr 19	NC_000019.10:g.40880797_40880799G[5]CGGGGGGG[1]
GRCh38.p14 chr 19	NC_000019.10:g.40880797_40880799dup
GRCh38.p14 chr 19	NC_000019.10:g.40880797_40880799G[6]CGGGGGG[1]
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880797_40880799G[8]CGGGG[1]
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGGGGGGGG
GRCh38.p14 chr 19	NC_000019.10:g.40880797_40880799G[8]TGGGG[1]
GRCh38.p14 chr 19	NC_000019.10:g.40880797_40880799G[5]TGGGGGG[1]
GRCh38.p14 chr 19	NC_000019.10:g.40880797_40880799G[5]TGGGGGGG[1]
GRCh38.p14 chr 19	NC_000019.10:g.40880799_40880800insTTGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386703_41386704del
GRCh37.p13 chr 19	NC_000019.9:g.41386702_41386704G[4]CGGGGGGGG[1]
GRCh37.p13 chr 19	NC_000019.9:g.41386703_41386704dup
GRCh37.p13 chr 19	NC_000019.9:g.41386702_41386704G[5]CGGGGGGG[1]
GRCh37.p13 chr 19	NC_000019.9:g.41386702_41386704dup
GRCh37.p13 chr 19	NC_000019.9:g.41386702_41386704G[6]CGGGGGG[1]
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386702_41386704G[8]CGGGG[1]
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386702_41386704G[8]TGGGG[1]
GRCh37.p13 chr 19	NC_000019.9:g.41386702_41386704G[5]TGGGGGG[1]
GRCh37.p13 chr 19	NC_000019.9:g.41386702_41386704G[5]TGGGGGGG[1]
GRCh37.p13 chr 19	NC_000019.9:g.41386704_41386705insTTGGGGGGG
CYP2A7 RefSeqGene	NG_007960.1:g.6955_6956del
CYP2A7 RefSeqGene	NG_007960.1:g.6954_6956C[8]GCCCC[1]
CYP2A7 RefSeqGene	NG_007960.1:g.6955_6956dup
CYP2A7 RefSeqGene	NG_007960.1:g.6954_6956C[7]GCCCCC[1]
CYP2A7 RefSeqGene	NG_007960.1:g.6954_6956dup
CYP2A7 RefSeqGene	NG_007960.1:g.6954_6956C[6]GCCCCCC[1]
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6954_6956C[4]GCCCCCCCC[1]
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCCCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCCCCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCCCCCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCCCCCCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCCCCCCCCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6956_6957insCCCCCCCCCCCCCCCCCC
CYP2A7 RefSeqGene	NG_007960.1:g.6954_6956C[4]ACCCCCCCC[1]
CYP2A7 RefSeqGene	NG_007960.1:g.6954_6956C[6]ACCCCC[1]
CYP2A7 RefSeqGene	NG_007960.1:g.6954_6956C[7]ACCCCC[1]
CYP2A7 RefSeqGene	NG_007960.1:g.6954_6956C[7]AACCC[1]

Gene: CYP2A7, cytochrome P450 family 2 subfamily A member 7 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CYP2A7 transcript variant 1	NM_000764.3:c.344-170_344… NM_000764.3:c.344-170_344-169del	N/A	Intron Variant
CYP2A7 transcript variant 2	NM_030589.3:c.191-170_191… NM_030589.3:c.191-170_191-169del	N/A	Intron Variant
CYP2A7 transcript variant X1	XM_047438279.1:c.344-170_… XM_047438279.1:c.344-170_344-169del	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	GGG=	delGG	insGC(G)₈	dupGG	insGGC(G)₇	dupGGG	insGGGC(G)₆	ins(G)₄	ins(G)₅C(G)₄	ins(G)₆	ins(G)₇	ins(G)₈	ins(G)₉	ins(G)₁₀	ins(G)₁₁	ins(G)₁₂	ins(G)₁₃	ins(G)₁₄	ins(G)₁₅	ins(G)₁₇	ins(G)₁₈	ins(G)₅T(G)₄	insGGT(G)₆	insGGT(G)₇	insTT(G)₇
GRCh38.p14 chr 19	NC_000019.10:g.40880797_40880799=	NC_000019.10:g.40880798_40880799del	NC_000019.10:g.40880797_40880799G[4]CGGGGGGGG[1]	NC_000019.10:g.40880798_40880799dup	NC_000019.10:g.40880797_40880799G[5]CGGGGGGG[1]	NC_000019.10:g.40880797_40880799dup	NC_000019.10:g.40880797_40880799G[6]CGGGGGG[1]	NC_000019.10:g.40880799_40880800insGGGG	NC_000019.10:g.40880797_40880799G[8]CGGGG[1]	NC_000019.10:g.40880799_40880800insGGGGGG	NC_000019.10:g.40880799_40880800insGGGGGGG	NC_000019.10:g.40880799_40880800insGGGGGGGG	NC_000019.10:g.40880799_40880800insGGGGGGGGG	NC_000019.10:g.40880799_40880800insGGGGGGGGGG	NC_000019.10:g.40880799_40880800insGGGGGGGGGGG	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGG	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGGG	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGGGG	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGGGGG	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGGGGGGG	NC_000019.10:g.40880799_40880800insGGGGGGGGGGGGGGGGGG	NC_000019.10:g.40880797_40880799G[8]TGGGG[1]	NC_000019.10:g.40880797_40880799G[5]TGGGGGG[1]	NC_000019.10:g.40880797_40880799G[5]TGGGGGGG[1]	NC_000019.10:g.40880799_40880800insTTGGGGGGG
GRCh37.p13 chr 19	NC_000019.9:g.41386702_41386704=	NC_000019.9:g.41386703_41386704del	NC_000019.9:g.41386702_41386704G[4]CGGGGGGGG[1]	NC_000019.9:g.41386703_41386704dup	NC_000019.9:g.41386702_41386704G[5]CGGGGGGG[1]	NC_000019.9:g.41386702_41386704dup	NC_000019.9:g.41386702_41386704G[6]CGGGGGG[1]	NC_000019.9:g.41386704_41386705insGGGG	NC_000019.9:g.41386702_41386704G[8]CGGGG[1]	NC_000019.9:g.41386704_41386705insGGGGGG	NC_000019.9:g.41386704_41386705insGGGGGGG	NC_000019.9:g.41386704_41386705insGGGGGGGG	NC_000019.9:g.41386704_41386705insGGGGGGGGG	NC_000019.9:g.41386704_41386705insGGGGGGGGGG	NC_000019.9:g.41386704_41386705insGGGGGGGGGGG	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGG	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGGG	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGGGG	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGGGGG	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGGGGGGG	NC_000019.9:g.41386704_41386705insGGGGGGGGGGGGGGGGGG	NC_000019.9:g.41386702_41386704G[8]TGGGG[1]	NC_000019.9:g.41386702_41386704G[5]TGGGGGG[1]	NC_000019.9:g.41386702_41386704G[5]TGGGGGGG[1]	NC_000019.9:g.41386704_41386705insTTGGGGGGG
CYP2A7 RefSeqGene	NG_007960.1:g.6954_6956=	NG_007960.1:g.6955_6956del	NG_007960.1:g.6954_6956C[8]GCCCC[1]	NG_007960.1:g.6955_6956dup	NG_007960.1:g.6954_6956C[7]GCCCCC[1]	NG_007960.1:g.6954_6956dup	NG_007960.1:g.6954_6956C[6]GCCCCCC[1]	NG_007960.1:g.6956_6957insCCCC	NG_007960.1:g.6954_6956C[4]GCCCCCCCC[1]	NG_007960.1:g.6956_6957insCCCCCC	NG_007960.1:g.6956_6957insCCCCCCC	NG_007960.1:g.6956_6957insCCCCCCCC	NG_007960.1:g.6956_6957insCCCCCCCCC	NG_007960.1:g.6956_6957insCCCCCCCCCC	NG_007960.1:g.6956_6957insCCCCCCCCCCC	NG_007960.1:g.6956_6957insCCCCCCCCCCCC	NG_007960.1:g.6956_6957insCCCCCCCCCCCCC	NG_007960.1:g.6956_6957insCCCCCCCCCCCCCC	NG_007960.1:g.6956_6957insCCCCCCCCCCCCCCC	NG_007960.1:g.6956_6957insCCCCCCCCCCCCCCCCC	NG_007960.1:g.6956_6957insCCCCCCCCCCCCCCCCCC	NG_007960.1:g.6954_6956C[4]ACCCCCCCC[1]	NG_007960.1:g.6954_6956C[6]ACCCCC[1]	NG_007960.1:g.6954_6956C[7]ACCCCC[1]	NG_007960.1:g.6954_6956C[7]AACCC[1]
CYP2A7 transcript variant 1	NM_000764.2:c.344-169=	NM_000764.2:c.344-170_344-169del	NM_000764.2:c.344-169_344-168insCCCCCCCCGC	NM_000764.2:c.344-170_344-169dup	NM_000764.2:c.344-169_344-168insCCCCCCCGCC	NM_000764.2:c.344-171_344-169dup	NM_000764.2:c.344-169_344-168insCCCCCCGCCC	NM_000764.2:c.344-169_344-168insCCCC	NM_000764.2:c.344-169_344-168insCCCCGCCCCC	NM_000764.2:c.344-169_344-168insCCCCCC	NM_000764.2:c.344-169_344-168insCCCCCCC	NM_000764.2:c.344-169_344-168insCCCCCCCC	NM_000764.2:c.344-169_344-168insCCCCCCCCC	NM_000764.2:c.344-169_344-168insCCCCCCCCCC	NM_000764.2:c.344-169_344-168insCCCCCCCCCCC	NM_000764.2:c.344-169_344-168insCCCCCCCCCCCC	NM_000764.2:c.344-169_344-168insCCCCCCCCCCCCC	NM_000764.2:c.344-169_344-168insCCCCCCCCCCCCCC	NM_000764.2:c.344-169_344-168insCCCCCCCCCCCCCCC	NM_000764.2:c.344-169_344-168insCCCCCCCCCCCCCCCCC	NM_000764.2:c.344-169_344-168insCCCCCCCCCCCCCCCCCC	NM_000764.2:c.344-169_344-168insCCCCACCCCC	NM_000764.2:c.344-169_344-168insCCCCCCACC	NM_000764.2:c.344-169_344-168insCCCCCCCACC	NM_000764.2:c.344-169_344-168insCCCCCCCAA
CYP2A7 transcript variant 1	NM_000764.3:c.344-169=	NM_000764.3:c.344-170_344-169del	NM_000764.3:c.344-169_344-168insCCCCCCCCGC	NM_000764.3:c.344-170_344-169dup	NM_000764.3:c.344-169_344-168insCCCCCCCGCC	NM_000764.3:c.344-171_344-169dup	NM_000764.3:c.344-169_344-168insCCCCCCGCCC	NM_000764.3:c.344-169_344-168insCCCC	NM_000764.3:c.344-169_344-168insCCCCGCCCCC	NM_000764.3:c.344-169_344-168insCCCCCC	NM_000764.3:c.344-169_344-168insCCCCCCC	NM_000764.3:c.344-169_344-168insCCCCCCCC	NM_000764.3:c.344-169_344-168insCCCCCCCCC	NM_000764.3:c.344-169_344-168insCCCCCCCCCC	NM_000764.3:c.344-169_344-168insCCCCCCCCCCC	NM_000764.3:c.344-169_344-168insCCCCCCCCCCCC	NM_000764.3:c.344-169_344-168insCCCCCCCCCCCCC	NM_000764.3:c.344-169_344-168insCCCCCCCCCCCCCC	NM_000764.3:c.344-169_344-168insCCCCCCCCCCCCCCC	NM_000764.3:c.344-169_344-168insCCCCCCCCCCCCCCCCC	NM_000764.3:c.344-169_344-168insCCCCCCCCCCCCCCCCCC	NM_000764.3:c.344-169_344-168insCCCCACCCCC	NM_000764.3:c.344-169_344-168insCCCCCCACC	NM_000764.3:c.344-169_344-168insCCCCCCCACC	NM_000764.3:c.344-169_344-168insCCCCCCCAA
CYP2A7 transcript variant 2	NM_030589.2:c.191-169=	NM_030589.2:c.191-170_191-169del	NM_030589.2:c.191-169_191-168insCCCCCCCCGC	NM_030589.2:c.191-170_191-169dup	NM_030589.2:c.191-169_191-168insCCCCCCCGCC	NM_030589.2:c.191-171_191-169dup	NM_030589.2:c.191-169_191-168insCCCCCCGCCC	NM_030589.2:c.191-169_191-168insCCCC	NM_030589.2:c.191-169_191-168insCCCCGCCCCC	NM_030589.2:c.191-169_191-168insCCCCCC	NM_030589.2:c.191-169_191-168insCCCCCCC	NM_030589.2:c.191-169_191-168insCCCCCCCC	NM_030589.2:c.191-169_191-168insCCCCCCCCC	NM_030589.2:c.191-169_191-168insCCCCCCCCCC	NM_030589.2:c.191-169_191-168insCCCCCCCCCCC	NM_030589.2:c.191-169_191-168insCCCCCCCCCCCC	NM_030589.2:c.191-169_191-168insCCCCCCCCCCCCC	NM_030589.2:c.191-169_191-168insCCCCCCCCCCCCCC	NM_030589.2:c.191-169_191-168insCCCCCCCCCCCCCCC	NM_030589.2:c.191-169_191-168insCCCCCCCCCCCCCCCCC	NM_030589.2:c.191-169_191-168insCCCCCCCCCCCCCCCCCC	NM_030589.2:c.191-169_191-168insCCCCACCCCC	NM_030589.2:c.191-169_191-168insCCCCCCACC	NM_030589.2:c.191-169_191-168insCCCCCCCACC	NM_030589.2:c.191-169_191-168insCCCCCCCAA
CYP2A7 transcript variant 2	NM_030589.3:c.191-169=	NM_030589.3:c.191-170_191-169del	NM_030589.3:c.191-169_191-168insCCCCCCCCGC	NM_030589.3:c.191-170_191-169dup	NM_030589.3:c.191-169_191-168insCCCCCCCGCC	NM_030589.3:c.191-171_191-169dup	NM_030589.3:c.191-169_191-168insCCCCCCGCCC	NM_030589.3:c.191-169_191-168insCCCC	NM_030589.3:c.191-169_191-168insCCCCGCCCCC	NM_030589.3:c.191-169_191-168insCCCCCC	NM_030589.3:c.191-169_191-168insCCCCCCC	NM_030589.3:c.191-169_191-168insCCCCCCCC	NM_030589.3:c.191-169_191-168insCCCCCCCCC	NM_030589.3:c.191-169_191-168insCCCCCCCCCC	NM_030589.3:c.191-169_191-168insCCCCCCCCCCC	NM_030589.3:c.191-169_191-168insCCCCCCCCCCCC	NM_030589.3:c.191-169_191-168insCCCCCCCCCCCCC	NM_030589.3:c.191-169_191-168insCCCCCCCCCCCCCC	NM_030589.3:c.191-169_191-168insCCCCCCCCCCCCCCC	NM_030589.3:c.191-169_191-168insCCCCCCCCCCCCCCCCC	NM_030589.3:c.191-169_191-168insCCCCCCCCCCCCCCCCCC	NM_030589.3:c.191-169_191-168insCCCCACCCCC	NM_030589.3:c.191-169_191-168insCCCCCCACC	NM_030589.3:c.191-169_191-168insCCCCCCCACC	NM_030589.3:c.191-169_191-168insCCCCCCCAA
CYP2A7 transcript variant X1	XM_047438279.1:c.344-169=	XM_047438279.1:c.344-170_344-169del	XM_047438279.1:c.344-169_344-168insCCCCCCCCGC	XM_047438279.1:c.344-170_344-169dup	XM_047438279.1:c.344-169_344-168insCCCCCCCGCC	XM_047438279.1:c.344-171_344-169dup	XM_047438279.1:c.344-169_344-168insCCCCCCGCCC	XM_047438279.1:c.344-169_344-168insCCCC	XM_047438279.1:c.344-169_344-168insCCCCGCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCCCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCCCCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCCCCCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCCCCCCCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCCCCCCCCCCCCC	XM_047438279.1:c.344-169_344-168insCCCCACCCCC	XM_047438279.1:c.344-169_344-168insCCCCCCACC	XM_047438279.1:c.344-169_344-168insCCCCCCCACC	XM_047438279.1:c.344-169_344-168insCCCCCCCAA

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#.

16 SubSNP, 11 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3702785040	Jul 13, 2019 (153)
2	EVA_DECODE	ss3702785041	Jul 13, 2019 (153)
3	EVA_DECODE	ss3702785042	Jul 13, 2019 (153)
4	EVA_DECODE	ss3702785043	Jul 13, 2019 (153)
5	EVA_DECODE	ss3702785044	Jul 13, 2019 (153)
6	EVA_DECODE	ss3702785045	Jul 13, 2019 (153)
7	KOGIC	ss3981369583	Apr 27, 2020 (154)
8	GNOMAD	ss4331371860	Apr 26, 2021 (155)
9	GNOMAD	ss4331371861	Apr 26, 2021 (155)
10	GNOMAD	ss4331371862	Apr 26, 2021 (155)
11	GNOMAD	ss4331371863	Apr 26, 2021 (155)
12	GNOMAD	ss4331371864	Apr 26, 2021 (155)
13	TOMMO_GENOMICS	ss5227800214	Apr 26, 2021 (155)
14	TOMMO_GENOMICS	ss5227800215	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5786446850	Oct 16, 2022 (156)
16	TOMMO_GENOMICS	ss5786446851	Oct 16, 2022 (156)
17	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540293585 (NC_000019.10:40880796::GG 4/21660) Row 540293586 (NC_000019.10:40880796::GGGGGGGGGG 3/21656) Row 540293587 (NC_000019.10:40880796::GGGGGGGGGGGGG 1/21660)...	-	Apr 26, 2021 (155)
18	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540293585 (NC_000019.10:40880796::GG 4/21660) Row 540293586 (NC_000019.10:40880796::GGGGGGGGGG 3/21656) Row 540293587 (NC_000019.10:40880796::GGGGGGGGGGGGG 1/21660)...	-	Apr 26, 2021 (155)
19	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540293585 (NC_000019.10:40880796::GG 4/21660) Row 540293586 (NC_000019.10:40880796::GGGGGGGGGG 3/21656) Row 540293587 (NC_000019.10:40880796::GGGGGGGGGGGGG 1/21660)...	-	Apr 26, 2021 (155)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540293585 (NC_000019.10:40880796::GG 4/21660) Row 540293586 (NC_000019.10:40880796::GGGGGGGGGG 3/21656) Row 540293587 (NC_000019.10:40880796::GGGGGGGGGGGGG 1/21660)...	-	Apr 26, 2021 (155)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 540293585 (NC_000019.10:40880796::GG 4/21660) Row 540293586 (NC_000019.10:40880796::GGGGGGGGGG 3/21656) Row 540293587 (NC_000019.10:40880796::GGGGGGGGGGGGG 1/21660)...	-	Apr 26, 2021 (155)
22	Korean Genome Project	NC_000019.10 - 40880797	Apr 27, 2020 (154)
23	8.3KJPN Submission ignored due to conflicting rows: Row 85769521 (NC_000019.9:41386701:GG: 59/8454) Row 85769522 (NC_000019.9:41386701::GG 3/8454)	-	Apr 26, 2021 (155)
24	8.3KJPN Submission ignored due to conflicting rows: Row 85769521 (NC_000019.9:41386701:GG: 59/8454) Row 85769522 (NC_000019.9:41386701::GG 3/8454)	-	Apr 26, 2021 (155)
25	14KJPN Submission ignored due to conflicting rows: Row 120283954 (NC_000019.10:40880796:GG: 110/15434) Row 120283955 (NC_000019.10:40880796::GG 2/15434)	-	Oct 16, 2022 (156)
26	14KJPN Submission ignored due to conflicting rows: Row 120283954 (NC_000019.10:40880796:GG: 110/15434) Row 120283955 (NC_000019.10:40880796::GG 2/15434)	-	Oct 16, 2022 (156)
27	ALFA	NC_000019.10 - 40880797	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:

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3293509879	NC_000019.10:40880796::GGGGGGGGCG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGCGGGG

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

No publications for rs1354151315

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

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5227800214	NC_000019.9:41386701:GG:	NC_000019.10:40880796:GGG:G	(self)
37747584, ss3981369583, ss4331371864, ss5786446850	NC_000019.10:40880796:GG:	NC_000019.10:40880796:GGG:G	(self)
9678957191	NC_000019.10:40880796:GGG:G	NC_000019.10:40880796:GGG:G	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGCGGG… NC_000019.10:40880796:GGG:GGGGCGGGGGGGG	NC_000019.10:40880796:GGG:GGGGCGGG… NC_000019.10:40880796:GGG:GGGGCGGGGGGGG	(self)
ss5227800215	NC_000019.9:41386701::GG	NC_000019.10:40880796:GGG:GGGGG	(self)
ss4331371860, ss5786446851	NC_000019.10:40880796::GG	NC_000019.10:40880796:GGG:GGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGG	NC_000019.10:40880796:GGG:GGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGCGG… NC_000019.10:40880796:GGG:GGGGGCGGGGGGG	NC_000019.10:40880796:GGG:GGGGGCGG… NC_000019.10:40880796:GGG:GGGGGCGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGG	NC_000019.10:40880796:GGG:GGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGCG… NC_000019.10:40880796:GGG:GGGGGGCGGGGGG	NC_000019.10:40880796:GGG:GGGGGGCG… NC_000019.10:40880796:GGG:GGGGGGCGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGG	NC_000019.10:40880796:GGG:GGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGCGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGCGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGG	(self)
ss3702785045	NC_000019.10:40880796::GGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGG	(self)
ss3702785044, ss4331371861	NC_000019.10:40880796::GGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGG	(self)
ss3702785043	NC_000019.10:40880796::GGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGG	(self)
ss3702785042	NC_000019.10:40880796::GGGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGG	(self)
ss4331371862	NC_000019.10:40880796::GGGGGGGGGGG… NC_000019.10:40880796::GGGGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGGGGG	(self)
ss3702785041	NC_000019.10:40880796::GGGGGGGGGGG… NC_000019.10:40880796::GGGGGGGGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGGGGGGG	(self)
ss3702785040	NC_000019.10:40880796::GGGGGGGGGGG… NC_000019.10:40880796::GGGGGGGGGGGGGGGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGGGGGGGGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGTGGGG	NC_000019.10:40880796:GGG:GGGGGGGG… NC_000019.10:40880796:GGG:GGGGGGGGTGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGTGG… NC_000019.10:40880796:GGG:GGGGGTGGGGGG	NC_000019.10:40880796:GGG:GGGGGTGG… NC_000019.10:40880796:GGG:GGGGGTGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGGGTGG… NC_000019.10:40880796:GGG:GGGGGTGGGGGGG	NC_000019.10:40880796:GGG:GGGGGTGG… NC_000019.10:40880796:GGG:GGGGGTGGGGGGG	(self)
ss4331371863	NC_000019.10:40880796::GGGTTGGGG	NC_000019.10:40880796:GGG:GGGTTGGG… NC_000019.10:40880796:GGG:GGGTTGGGGGGG	(self)
9678957191	NC_000019.10:40880796:GGG:GGGTTGGG… NC_000019.10:40880796:GGG:GGGTTGGGGGGG	NC_000019.10:40880796:GGG:GGGTTGGG… NC_000019.10:40880796:GGG:GGGTTGGGGGGG	(self)

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1354151315