Name: rs1491475267
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.

rs1491475267

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:154180415-154180416 (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: insA / insATA / insATATA / ins(AT)…
insA / insATA / insATATA / ins(AT)₃A / ins(AT)₄A / ins(AT)₅A / ins(AT)₆A / ins(AT)₇A / ins(AT)₈A / ins(AT)₉A / ins(AT)₁₀A / ins(AT)₆C
Variation Type: Insertion
Frequency: insA=0.00420 (82/19506, 14KJPN)
insA=0.00000 (0/11822, ALFA)
insATA=0.00000 (0/11822, ALFA) (+ 10 more)
insATATA=0.00000 (0/11822, ALFA)
ins(AT)₃A=0.00000 (0/11822, ALFA)
ins(AT)₄A=0.00000 (0/11822, ALFA)
ins(AT)₅A=0.00000 (0/11822, ALFA)
ins(AT)₆A=0.00000 (0/11822, ALFA)
ins(AT)₇A=0.00000 (0/11822, ALFA)
ins(AT)₈A=0.00000 (0/11822, ALFA)
ins(AT)₉A=0.00000 (0/11822, ALFA)
ins(AT)₁₀A=0.00000 (0/11822, ALFA)
insA=0.0099 (62/6246, 8.3KJPN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: OPRM1 : Intron Variant
IPCEF1 : 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	11822	=1.00000	A=0.00000, ATA=0.00000, ATATA=0.00000, ATATATA=0.00000, ATATATATA=0.00000, ATATATATATA=0.00000, ATATATATATATA=0.00000, ATATATATATATATA=0.00000, ATATATATATATATATA=0.00000, ATATATATATATATATATA=0.00000, ATATATATATATATATATATA=0.00000	1.0	N/A
European	Sub	7614	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATA=0.0000, ATATATATATATA=0.0000, ATATATATATATATA=0.0000, ATATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000, ATATATATATATATATATATA=0.0000	1.0	N/A
African	Sub	2782	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATA=0.0000, ATATATATATATA=0.0000, ATATATATATATATA=0.0000, ATATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000, ATATATATATATATATATATA=0.0000	1.0	N/A
African Others	Sub	104	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000, ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000	1.0	N/A
African American	Sub	2678	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATA=0.0000, ATATATATATATA=0.0000, ATATATATATATATA=0.0000, ATATATATATATATATA=0.0000, ATATATATATATATATATA=0.0000, ATATATATATATATATATATA=0.0000	1.0	N/A
Asian	Sub	108	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000, ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000	1.0	N/A
East Asian	Sub	84	=1.00	A=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATA=0.00, ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00	1.0	N/A
Other Asian	Sub	24	=1.00	A=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATA=0.00, ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00	1.0	N/A
Latin American 1	Sub	146	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000, ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000	1.0	N/A
Latin American 2	Sub	610	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000, ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000	1.0	N/A
South Asian	Sub	94	=1.00	A=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATA=0.00, ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00	1.0	N/A
Other	Sub	468	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000, ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
14KJPN	JAPANESE	Study-wide	19506	- No frequency provided	insA=0.00420
Allele Frequency Aggregator	Total	Global	11822	- No frequency provided	insA=0.00000, insATA=0.00000, insATATA=0.00000, ins(AT)₃A=0.00000, ins(AT)₄A=0.00000, ins(AT)₅A=0.00000, ins(AT)₆A=0.00000, ins(AT)₇A=0.00000, ins(AT)₈A=0.00000, ins(AT)₉A=0.00000, ins(AT)₁₀A=0.00000
Allele Frequency Aggregator	European	Sub	7614	- No frequency provided	insA=0.0000, insATA=0.0000, insATATA=0.0000, ins(AT)₃A=0.0000, ins(AT)₄A=0.0000, ins(AT)₅A=0.0000, ins(AT)₆A=0.0000, ins(AT)₇A=0.0000, ins(AT)₈A=0.0000, ins(AT)₉A=0.0000, ins(AT)₁₀A=0.0000
Allele Frequency Aggregator	African	Sub	2782	- No frequency provided	insA=0.0000, insATA=0.0000, insATATA=0.0000, ins(AT)₃A=0.0000, ins(AT)₄A=0.0000, ins(AT)₅A=0.0000, ins(AT)₆A=0.0000, ins(AT)₇A=0.0000, ins(AT)₈A=0.0000, ins(AT)₉A=0.0000, ins(AT)₁₀A=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000, ins(AT)₆A=0.000, ins(AT)₇A=0.000, ins(AT)₈A=0.000, ins(AT)₉A=0.000, ins(AT)₁₀A=0.000
Allele Frequency Aggregator	Other	Sub	468	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000, ins(AT)₆A=0.000, ins(AT)₇A=0.000, ins(AT)₈A=0.000, ins(AT)₉A=0.000, ins(AT)₁₀A=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000, ins(AT)₆A=0.000, ins(AT)₇A=0.000, ins(AT)₈A=0.000, ins(AT)₉A=0.000, ins(AT)₁₀A=0.000
Allele Frequency Aggregator	Asian	Sub	108	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000, ins(AT)₆A=0.000, ins(AT)₇A=0.000, ins(AT)₈A=0.000, ins(AT)₉A=0.000, ins(AT)₁₀A=0.000
Allele Frequency Aggregator	South Asian	Sub	94	- No frequency provided	insA=0.00, insATA=0.00, insATATA=0.00, ins(AT)₃A=0.00, ins(AT)₄A=0.00, ins(AT)₅A=0.00, ins(AT)₆A=0.00, ins(AT)₇A=0.00, ins(AT)₈A=0.00, ins(AT)₉A=0.00, ins(AT)₁₀A=0.00
8.3KJPN	JAPANESE	Study-wide	6246	- No frequency provided	insA=0.0099

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 6	NC_000006.12:g.154180415_154180416insA
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416insATA
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416insATATA
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416insATATATA
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416insATATATATA
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416insATATATATATA
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416insATATATATATATA
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416insATATATATATATATA
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416insATATATATATATATATA
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416insATATATATATATATATATA
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416insATATATATATATATATATATA
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416insATATATATATATC
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insA
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insATA
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insATATA
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insATATATA
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insATATATATA
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insATATATATATA
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insATATATATATATA
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insATATATATATATATA
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insATATATATATATATATA
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insATATATATATATATATATA
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insATATATATATATATATATATA
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550insATATATATATATC
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insATA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insATATA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insATATATA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insATATATATA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insATATATATATA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insATATATATATATA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insATATATATATATATA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insATATATATATATATATA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insATATATATATATATATATA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insATATATATATATATATATATA
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916insATATATATATATC

Gene: OPRM1, opioid receptor mu 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
OPRM1 transcript variant MOR-1O	NM_001008503.3:c.1165-662… NM_001008503.3:c.1165-66278_1165-66277insA	N/A	Intron Variant
OPRM1 transcript variant MOR-1	NM_000914.5:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1A	NM_001008504.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1X	NM_001008505.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1i	NM_001145279.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1G1	NM_001145280.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1G2	NM_001145281.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B1	NM_001145282.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B2	NM_001145283.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B3	NM_001145284.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B4	NM_001145285.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1B5	NM_001145286.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1K1	NM_001145287.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1S	NM_001285522.1:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1A2	NM_001285523.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1CA	NM_001285524.1:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1K2	NM_001285526.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1W	NM_001285527.1:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-3	NM_001285528.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Y3	NR_104348.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Y2	NR_104349.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Z	NR_104350.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant MOR-1Y	NR_104351.1:n.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X2	XM_011535851.4:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X3	XM_011535853.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X5	XM_011535856.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X7	XM_011535862.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X1	XM_017010903.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X4	XM_017010904.2:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X8	XM_017010907.3:c.	N/A	Genic Downstream Transcript Variant
OPRM1 transcript variant X6	XM_047418837.1:c.	N/A	Genic Downstream Transcript Variant

Gene: IPCEF1, interaction protein for cytohesin exchange factors 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IPCEF1 transcript variant 1	NM_001130699.2:c.911-1230… NM_001130699.2:c.911-12303_911-12302insT	N/A	Intron Variant
IPCEF1 transcript variant 2	NM_001130700.2:c.911-1230… NM_001130700.2:c.911-12303_911-12302insT	N/A	Intron Variant
IPCEF1 transcript variant 4	NM_001394799.1:c.911-1230… NM_001394799.1:c.911-12303_911-12302insT	N/A	Intron Variant
IPCEF1 transcript variant 5	NM_001394800.1:c.911-1230… NM_001394800.1:c.911-12303_911-12302insT	N/A	Intron Variant
IPCEF1 transcript variant 6	NM_001394801.1:c.911-1230… NM_001394801.1:c.911-12303_911-12302insT	N/A	Intron Variant
IPCEF1 transcript variant 7	NM_001394802.1:c.908-1230… NM_001394802.1:c.908-12303_908-12302insT	N/A	Intron Variant
IPCEF1 transcript variant 3	NM_015553.3:c.908-12303_9… NM_015553.3:c.908-12303_908-12302insT	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	=	insA	insATA	insATATA	ins(AT)₃A	ins(AT)₄A	ins(AT)₅A	ins(AT)₆A	ins(AT)₇A	ins(AT)₈A	ins(AT)₉A	ins(AT)₁₀A	ins(AT)₆C
GRCh38.p14 chr 6	NC_000006.12:g.154180415_154180416=	NC_000006.12:g.154180415_154180416insA	NC_000006.12:g.154180415_154180416insATA	NC_000006.12:g.154180415_154180416insATATA	NC_000006.12:g.154180415_154180416insATATATA	NC_000006.12:g.154180415_154180416insATATATATA	NC_000006.12:g.154180415_154180416insATATATATATA	NC_000006.12:g.154180415_154180416insATATATATATATA	NC_000006.12:g.154180415_154180416insATATATATATATATA	NC_000006.12:g.154180415_154180416insATATATATATATATATA	NC_000006.12:g.154180415_154180416insATATATATATATATATATA	NC_000006.12:g.154180415_154180416insATATATATATATATATATATA	NC_000006.12:g.154180415_154180416insATATATATATATC
GRCh37.p13 chr 6	NC_000006.11:g.154501549_154501550=	NC_000006.11:g.154501549_154501550insA	NC_000006.11:g.154501549_154501550insATA	NC_000006.11:g.154501549_154501550insATATA	NC_000006.11:g.154501549_154501550insATATATA	NC_000006.11:g.154501549_154501550insATATATATA	NC_000006.11:g.154501549_154501550insATATATATATA	NC_000006.11:g.154501549_154501550insATATATATATATA	NC_000006.11:g.154501549_154501550insATATATATATATATA	NC_000006.11:g.154501549_154501550insATATATATATATATATA	NC_000006.11:g.154501549_154501550insATATATATATATATATATA	NC_000006.11:g.154501549_154501550insATATATATATATATATATATA	NC_000006.11:g.154501549_154501550insATATATATATATC
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.174915_174916=	NG_021208.2:g.174915_174916insA	NG_021208.2:g.174915_174916insATA	NG_021208.2:g.174915_174916insATATA	NG_021208.2:g.174915_174916insATATATA	NG_021208.2:g.174915_174916insATATATATA	NG_021208.2:g.174915_174916insATATATATATA	NG_021208.2:g.174915_174916insATATATATATATA	NG_021208.2:g.174915_174916insATATATATATATATA	NG_021208.2:g.174915_174916insATATATATATATATATA	NG_021208.2:g.174915_174916insATATATATATATATATATA	NG_021208.2:g.174915_174916insATATATATATATATATATATA	NG_021208.2:g.174915_174916insATATATATATATC
OPRM1 transcript variant MOR-1O	NM_001008503.1:c.1165-66277=	NM_001008503.1:c.1165-66278_1165-66277insA	NM_001008503.1:c.1165-66278_1165-66277insATA	NM_001008503.1:c.1165-66278_1165-66277insATATA	NM_001008503.1:c.1165-66278_1165-66277insATATATA	NM_001008503.1:c.1165-66278_1165-66277insATATATATA	NM_001008503.1:c.1165-66278_1165-66277insATATATATATA	NM_001008503.1:c.1165-66278_1165-66277insATATATATATATA	NM_001008503.1:c.1165-66278_1165-66277insATATATATATATATA	NM_001008503.1:c.1165-66278_1165-66277insATATATATATATATATA	NM_001008503.1:c.1165-66278_1165-66277insATATATATATATATATATA	NM_001008503.1:c.1165-66278_1165-66277insATATATATATATATATATATA	NM_001008503.1:c.1165-66278_1165-66277insATATATATATATC
OPRM1 transcript variant MOR-1O	NM_001008503.3:c.1165-66277=	NM_001008503.3:c.1165-66278_1165-66277insA	NM_001008503.3:c.1165-66278_1165-66277insATA	NM_001008503.3:c.1165-66278_1165-66277insATATA	NM_001008503.3:c.1165-66278_1165-66277insATATATA	NM_001008503.3:c.1165-66278_1165-66277insATATATATA	NM_001008503.3:c.1165-66278_1165-66277insATATATATATA	NM_001008503.3:c.1165-66278_1165-66277insATATATATATATA	NM_001008503.3:c.1165-66278_1165-66277insATATATATATATATA	NM_001008503.3:c.1165-66278_1165-66277insATATATATATATATATA	NM_001008503.3:c.1165-66278_1165-66277insATATATATATATATATATA	NM_001008503.3:c.1165-66278_1165-66277insATATATATATATATATATATA	NM_001008503.3:c.1165-66278_1165-66277insATATATATATATC
IPCEF1 transcript variant 1	NM_001130699.1:c.911-12302=	NM_001130699.1:c.911-12302_911-12301insT	NM_001130699.1:c.911-12302_911-12301insTAT	NM_001130699.1:c.911-12302_911-12301insTATAT	NM_001130699.1:c.911-12302_911-12301insTATATAT	NM_001130699.1:c.911-12302_911-12301insTATATATAT	NM_001130699.1:c.911-12302_911-12301insTATATATATAT	NM_001130699.1:c.911-12302_911-12301insTATATATATATAT	NM_001130699.1:c.911-12302_911-12301insTATATATATATATAT	NM_001130699.1:c.911-12302_911-12301insTATATATATATATATAT	NM_001130699.1:c.911-12302_911-12301insTATATATATATATATATAT	NM_001130699.1:c.911-12302_911-12301insTATATATATATATATATATAT	NM_001130699.1:c.911-12302_911-12301insGATATATATATAT
IPCEF1 transcript variant 1	NM_001130699.2:c.911-12303=	NM_001130699.2:c.911-12303_911-12302insT	NM_001130699.2:c.911-12303_911-12302insTAT	NM_001130699.2:c.911-12303_911-12302insTATAT	NM_001130699.2:c.911-12303_911-12302insTATATAT	NM_001130699.2:c.911-12303_911-12302insTATATATAT	NM_001130699.2:c.911-12303_911-12302insTATATATATAT	NM_001130699.2:c.911-12303_911-12302insTATATATATATAT	NM_001130699.2:c.911-12303_911-12302insTATATATATATATAT	NM_001130699.2:c.911-12303_911-12302insTATATATATATATATAT	NM_001130699.2:c.911-12303_911-12302insTATATATATATATATATAT	NM_001130699.2:c.911-12303_911-12302insTATATATATATATATATATAT	NM_001130699.2:c.911-12303_911-12302insGATATATATATAT
IPCEF1 transcript variant 2	NM_001130700.1:c.911-12302=	NM_001130700.1:c.911-12302_911-12301insT	NM_001130700.1:c.911-12302_911-12301insTAT	NM_001130700.1:c.911-12302_911-12301insTATAT	NM_001130700.1:c.911-12302_911-12301insTATATAT	NM_001130700.1:c.911-12302_911-12301insTATATATAT	NM_001130700.1:c.911-12302_911-12301insTATATATATAT	NM_001130700.1:c.911-12302_911-12301insTATATATATATAT	NM_001130700.1:c.911-12302_911-12301insTATATATATATATAT	NM_001130700.1:c.911-12302_911-12301insTATATATATATATATAT	NM_001130700.1:c.911-12302_911-12301insTATATATATATATATATAT	NM_001130700.1:c.911-12302_911-12301insTATATATATATATATATATAT	NM_001130700.1:c.911-12302_911-12301insGATATATATATAT
IPCEF1 transcript variant 2	NM_001130700.2:c.911-12303=	NM_001130700.2:c.911-12303_911-12302insT	NM_001130700.2:c.911-12303_911-12302insTAT	NM_001130700.2:c.911-12303_911-12302insTATAT	NM_001130700.2:c.911-12303_911-12302insTATATAT	NM_001130700.2:c.911-12303_911-12302insTATATATAT	NM_001130700.2:c.911-12303_911-12302insTATATATATAT	NM_001130700.2:c.911-12303_911-12302insTATATATATATAT	NM_001130700.2:c.911-12303_911-12302insTATATATATATATAT	NM_001130700.2:c.911-12303_911-12302insTATATATATATATATAT	NM_001130700.2:c.911-12303_911-12302insTATATATATATATATATAT	NM_001130700.2:c.911-12303_911-12302insTATATATATATATATATATAT	NM_001130700.2:c.911-12303_911-12302insGATATATATATAT
IPCEF1 transcript variant 4	NM_001394799.1:c.911-12303=	NM_001394799.1:c.911-12303_911-12302insT	NM_001394799.1:c.911-12303_911-12302insTAT	NM_001394799.1:c.911-12303_911-12302insTATAT	NM_001394799.1:c.911-12303_911-12302insTATATAT	NM_001394799.1:c.911-12303_911-12302insTATATATAT	NM_001394799.1:c.911-12303_911-12302insTATATATATAT	NM_001394799.1:c.911-12303_911-12302insTATATATATATAT	NM_001394799.1:c.911-12303_911-12302insTATATATATATATAT	NM_001394799.1:c.911-12303_911-12302insTATATATATATATATAT	NM_001394799.1:c.911-12303_911-12302insTATATATATATATATATAT	NM_001394799.1:c.911-12303_911-12302insTATATATATATATATATATAT	NM_001394799.1:c.911-12303_911-12302insGATATATATATAT
IPCEF1 transcript variant 5	NM_001394800.1:c.911-12303=	NM_001394800.1:c.911-12303_911-12302insT	NM_001394800.1:c.911-12303_911-12302insTAT	NM_001394800.1:c.911-12303_911-12302insTATAT	NM_001394800.1:c.911-12303_911-12302insTATATAT	NM_001394800.1:c.911-12303_911-12302insTATATATAT	NM_001394800.1:c.911-12303_911-12302insTATATATATAT	NM_001394800.1:c.911-12303_911-12302insTATATATATATAT	NM_001394800.1:c.911-12303_911-12302insTATATATATATATAT	NM_001394800.1:c.911-12303_911-12302insTATATATATATATATAT	NM_001394800.1:c.911-12303_911-12302insTATATATATATATATATAT	NM_001394800.1:c.911-12303_911-12302insTATATATATATATATATATAT	NM_001394800.1:c.911-12303_911-12302insGATATATATATAT
IPCEF1 transcript variant 6	NM_001394801.1:c.911-12303=	NM_001394801.1:c.911-12303_911-12302insT	NM_001394801.1:c.911-12303_911-12302insTAT	NM_001394801.1:c.911-12303_911-12302insTATAT	NM_001394801.1:c.911-12303_911-12302insTATATAT	NM_001394801.1:c.911-12303_911-12302insTATATATAT	NM_001394801.1:c.911-12303_911-12302insTATATATATAT	NM_001394801.1:c.911-12303_911-12302insTATATATATATAT	NM_001394801.1:c.911-12303_911-12302insTATATATATATATAT	NM_001394801.1:c.911-12303_911-12302insTATATATATATATATAT	NM_001394801.1:c.911-12303_911-12302insTATATATATATATATATAT	NM_001394801.1:c.911-12303_911-12302insTATATATATATATATATATAT	NM_001394801.1:c.911-12303_911-12302insGATATATATATAT
IPCEF1 transcript variant 7	NM_001394802.1:c.908-12303=	NM_001394802.1:c.908-12303_908-12302insT	NM_001394802.1:c.908-12303_908-12302insTAT	NM_001394802.1:c.908-12303_908-12302insTATAT	NM_001394802.1:c.908-12303_908-12302insTATATAT	NM_001394802.1:c.908-12303_908-12302insTATATATAT	NM_001394802.1:c.908-12303_908-12302insTATATATATAT	NM_001394802.1:c.908-12303_908-12302insTATATATATATAT	NM_001394802.1:c.908-12303_908-12302insTATATATATATATAT	NM_001394802.1:c.908-12303_908-12302insTATATATATATATATAT	NM_001394802.1:c.908-12303_908-12302insTATATATATATATATATAT	NM_001394802.1:c.908-12303_908-12302insTATATATATATATATATATAT	NM_001394802.1:c.908-12303_908-12302insGATATATATATAT
IPCEF1 transcript variant 3	NM_015553.2:c.908-12302=	NM_015553.2:c.908-12302_908-12301insT	NM_015553.2:c.908-12302_908-12301insTAT	NM_015553.2:c.908-12302_908-12301insTATAT	NM_015553.2:c.908-12302_908-12301insTATATAT	NM_015553.2:c.908-12302_908-12301insTATATATAT	NM_015553.2:c.908-12302_908-12301insTATATATATAT	NM_015553.2:c.908-12302_908-12301insTATATATATATAT	NM_015553.2:c.908-12302_908-12301insTATATATATATATAT	NM_015553.2:c.908-12302_908-12301insTATATATATATATATAT	NM_015553.2:c.908-12302_908-12301insTATATATATATATATATAT	NM_015553.2:c.908-12302_908-12301insTATATATATATATATATATAT	NM_015553.2:c.908-12302_908-12301insGATATATATATAT
IPCEF1 transcript variant 3	NM_015553.3:c.908-12303=	NM_015553.3:c.908-12303_908-12302insT	NM_015553.3:c.908-12303_908-12302insTAT	NM_015553.3:c.908-12303_908-12302insTATAT	NM_015553.3:c.908-12303_908-12302insTATATAT	NM_015553.3:c.908-12303_908-12302insTATATATAT	NM_015553.3:c.908-12303_908-12302insTATATATATAT	NM_015553.3:c.908-12303_908-12302insTATATATATATAT	NM_015553.3:c.908-12303_908-12302insTATATATATATATAT	NM_015553.3:c.908-12303_908-12302insTATATATATATATATAT	NM_015553.3:c.908-12303_908-12302insTATATATATATATATATAT	NM_015553.3:c.908-12303_908-12302insTATATATATATATATATATAT	NM_015553.3:c.908-12303_908-12302insGATATATATATAT
IPCEF1 transcript variant X1	XM_005266919.1:c.911-12302=	XM_005266919.1:c.911-12302_911-12301insT	XM_005266919.1:c.911-12302_911-12301insTAT	XM_005266919.1:c.911-12302_911-12301insTATAT	XM_005266919.1:c.911-12302_911-12301insTATATAT	XM_005266919.1:c.911-12302_911-12301insTATATATAT	XM_005266919.1:c.911-12302_911-12301insTATATATATAT	XM_005266919.1:c.911-12302_911-12301insTATATATATATAT	XM_005266919.1:c.911-12302_911-12301insTATATATATATATAT	XM_005266919.1:c.911-12302_911-12301insTATATATATATATATAT	XM_005266919.1:c.911-12302_911-12301insTATATATATATATATATAT	XM_005266919.1:c.911-12302_911-12301insTATATATATATATATATATAT	XM_005266919.1:c.911-12302_911-12301insGATATATATATAT
IPCEF1 transcript variant X2	XM_005266920.1:c.911-12302=	XM_005266920.1:c.911-12302_911-12301insT	XM_005266920.1:c.911-12302_911-12301insTAT	XM_005266920.1:c.911-12302_911-12301insTATAT	XM_005266920.1:c.911-12302_911-12301insTATATAT	XM_005266920.1:c.911-12302_911-12301insTATATATAT	XM_005266920.1:c.911-12302_911-12301insTATATATATAT	XM_005266920.1:c.911-12302_911-12301insTATATATATATAT	XM_005266920.1:c.911-12302_911-12301insTATATATATATATAT	XM_005266920.1:c.911-12302_911-12301insTATATATATATATATAT	XM_005266920.1:c.911-12302_911-12301insTATATATATATATATATAT	XM_005266920.1:c.911-12302_911-12301insTATATATATATATATATATAT	XM_005266920.1:c.911-12302_911-12301insGATATATATATAT
IPCEF1 transcript variant X3	XM_005266921.1:c.911-12302=	XM_005266921.1:c.911-12302_911-12301insT	XM_005266921.1:c.911-12302_911-12301insTAT	XM_005266921.1:c.911-12302_911-12301insTATAT	XM_005266921.1:c.911-12302_911-12301insTATATAT	XM_005266921.1:c.911-12302_911-12301insTATATATAT	XM_005266921.1:c.911-12302_911-12301insTATATATATAT	XM_005266921.1:c.911-12302_911-12301insTATATATATATAT	XM_005266921.1:c.911-12302_911-12301insTATATATATATATAT	XM_005266921.1:c.911-12302_911-12301insTATATATATATATATAT	XM_005266921.1:c.911-12302_911-12301insTATATATATATATATATAT	XM_005266921.1:c.911-12302_911-12301insTATATATATATATATATATAT	XM_005266921.1:c.911-12302_911-12301insGATATATATATAT
IPCEF1 transcript variant X4	XM_005266922.1:c.911-12302=	XM_005266922.1:c.911-12302_911-12301insT	XM_005266922.1:c.911-12302_911-12301insTAT	XM_005266922.1:c.911-12302_911-12301insTATAT	XM_005266922.1:c.911-12302_911-12301insTATATAT	XM_005266922.1:c.911-12302_911-12301insTATATATAT	XM_005266922.1:c.911-12302_911-12301insTATATATATAT	XM_005266922.1:c.911-12302_911-12301insTATATATATATAT	XM_005266922.1:c.911-12302_911-12301insTATATATATATATAT	XM_005266922.1:c.911-12302_911-12301insTATATATATATATATAT	XM_005266922.1:c.911-12302_911-12301insTATATATATATATATATAT	XM_005266922.1:c.911-12302_911-12301insTATATATATATATATATATAT	XM_005266922.1:c.911-12302_911-12301insGATATATATATAT
IPCEF1 transcript variant X5	XM_005266923.1:c.908-12302=	XM_005266923.1:c.908-12302_908-12301insT	XM_005266923.1:c.908-12302_908-12301insTAT	XM_005266923.1:c.908-12302_908-12301insTATAT	XM_005266923.1:c.908-12302_908-12301insTATATAT	XM_005266923.1:c.908-12302_908-12301insTATATATAT	XM_005266923.1:c.908-12302_908-12301insTATATATATAT	XM_005266923.1:c.908-12302_908-12301insTATATATATATAT	XM_005266923.1:c.908-12302_908-12301insTATATATATATATAT	XM_005266923.1:c.908-12302_908-12301insTATATATATATATATAT	XM_005266923.1:c.908-12302_908-12301insTATATATATATATATATAT	XM_005266923.1:c.908-12302_908-12301insTATATATATATATATATATAT	XM_005266923.1:c.908-12302_908-12301insGATATATATATAT

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, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GNOMAD	ss4154404103	Apr 26, 2021 (155)
2	GNOMAD	ss4154404104	Apr 26, 2021 (155)
3	GNOMAD	ss4154404105	Apr 26, 2021 (155)
4	GNOMAD	ss4154404106	Apr 26, 2021 (155)
5	GNOMAD	ss4154404107	Apr 26, 2021 (155)
6	GNOMAD	ss4154404108	Apr 26, 2021 (155)
7	GNOMAD	ss4154404109	Apr 26, 2021 (155)
8	GNOMAD	ss4154404110	Apr 26, 2021 (155)
9	GNOMAD	ss4154404111	Apr 26, 2021 (155)
10	GNOMAD	ss4154404112	Apr 26, 2021 (155)
11	GNOMAD	ss4154404113	Apr 26, 2021 (155)
12	GNOMAD	ss4154404114	Apr 26, 2021 (155)
13	TOMMO_GENOMICS	ss5180698946	Apr 26, 2021 (155)
14	HUGCELL_USP	ss5468347558	Oct 14, 2022 (156)
15	TOMMO_GENOMICS	ss5719800434	Oct 14, 2022 (156)
16	YY_MCH	ss5808108740	Oct 14, 2022 (156)
17	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
18	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
19	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
22	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
23	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246112193 (NC_000006.12:154180415::A 2489/26602) Row 246112194 (NC_000006.12:154180415::ATA 22/27176) Row 246112195 (NC_000006.12:154180415::ATATA 23/27174)...	-	Apr 26, 2021 (155)
29	8.3KJPN	NC_000006.11 - 154501550	Apr 26, 2021 (155)
30	14KJPN	NC_000006.12 - 154180416	Oct 14, 2022 (156)
31	ALFA	NC_000006.12 - 154180416	Apr 26, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
38668253, ss5180698946	NC_000006.11:154501549::A	NC_000006.12:154180415::A	(self)
53637538, 378459074, ss4154404103, ss5468347558, ss5719800434, ss5808108740	NC_000006.12:154180415::A	NC_000006.12:154180415::A	(self)
378459074, ss4154404104	NC_000006.12:154180415::ATA	NC_000006.12:154180415::ATA	(self)
378459074, ss4154404105	NC_000006.12:154180415::ATATA	NC_000006.12:154180415::ATATA	(self)
378459074, ss4154404106	NC_000006.12:154180415::ATATATA	NC_000006.12:154180415::ATATATA	(self)
378459074, ss4154404107	NC_000006.12:154180415::ATATATATA	NC_000006.12:154180415::ATATATATA	(self)
378459074, ss4154404108	NC_000006.12:154180415::ATATATATATA	NC_000006.12:154180415::ATATATATATA	(self)
378459074, ss4154404109	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATA	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATA	(self)
378459074, ss4154404110	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATATA	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATATA	(self)
378459074, ss4154404111	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATATATA	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATATATA	(self)
378459074, ss4154404112	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATATATATA	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATATATATA	(self)
378459074, ss4154404113	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATATATATATA	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATATATATATA	(self)
ss4154404114	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATC	NC_000006.12:154180415::ATATATATAT… NC_000006.12:154180415::ATATATATATATC	(self)

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

No publications for rs1491475267

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

rs1491475267