Name: rs373120574
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.

rs373120574

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:154019748-154019765 (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)₉ / del(T)₅ / del(T)₄ / delT…
del(T)₉ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₁₇ / ins(T)₂₀ / ins(T)₂₁ / ins(T)₂₂
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₉=0.000008 (2/264690, TOPMED)
dup(T)₅=0.00577 (88/15250, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: OPRM1 : 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	15250	TTTTTTTTTTTTTTTTTT=0.98970	TTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00197, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00577, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00210, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00046, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.989509	0.001062	0.009429	32
European	Sub	11736	TTTTTTTTTTTTTTTTTT=0.98662	TTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00256, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00750, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00273, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00060, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.986316	0.001386	0.012299	32
African	Sub	2172	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	86	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	2086	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	100	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	78	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	22	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	130	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	594	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	88	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	430	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(T)₁₈=0.999992	del(T)₉=0.000008
Allele Frequency Aggregator	Total	Global	15250	(T)₁₈=0.98970	del(T)₉=0.00000, del(T)₅=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00197, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00577, dup(T)₆=0.00000, dup(T)₇=0.00000, dup(T)₁₀=0.00210, dup(T)₁₅=0.00046
Allele Frequency Aggregator	European	Sub	11736	(T)₁₈=0.98662	del(T)₉=0.00000, del(T)₅=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00256, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00750, dup(T)₆=0.00000, dup(T)₇=0.00000, dup(T)₁₀=0.00273, dup(T)₁₅=0.00060
Allele Frequency Aggregator	African	Sub	2172	(T)₁₈=1.0000	del(T)₉=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)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₁₀=0.0000, dup(T)₁₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	594	(T)₁₈=1.000	del(T)₉=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)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₁₀=0.000, dup(T)₁₅=0.000
Allele Frequency Aggregator	Other	Sub	430	(T)₁₈=1.000	del(T)₉=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)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₁₀=0.000, dup(T)₁₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	130	(T)₁₈=1.000	del(T)₉=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)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₁₀=0.000, dup(T)₁₅=0.000
Allele Frequency Aggregator	Asian	Sub	100	(T)₁₈=1.00	del(T)₉=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)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₁₀=0.00, dup(T)₁₅=0.00
Allele Frequency Aggregator	South Asian	Sub	88	(T)₁₈=1.00	del(T)₉=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)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₁₀=0.00, dup(T)₁₅=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 6	NC_000006.12:g.154019757_154019765del
GRCh38.p14 chr 6	NC_000006.12:g.154019761_154019765del
GRCh38.p14 chr 6	NC_000006.12:g.154019762_154019765del
GRCh38.p14 chr 6	NC_000006.12:g.154019763_154019765del
GRCh38.p14 chr 6	NC_000006.12:g.154019764_154019765del
GRCh38.p14 chr 6	NC_000006.12:g.154019765del
GRCh38.p14 chr 6	NC_000006.12:g.154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019764_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019763_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019762_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019761_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019760_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019759_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019758_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019757_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019756_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019755_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019754_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019752_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019751_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019750_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019749_154019765dup
GRCh38.p14 chr 6	NC_000006.12:g.154019765_154019766insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6	NC_000006.12:g.154019765_154019766insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 6	NC_000006.12:g.154019765_154019766insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.154340892_154340900del
GRCh37.p13 chr 6	NC_000006.11:g.154340896_154340900del
GRCh37.p13 chr 6	NC_000006.11:g.154340897_154340900del
GRCh37.p13 chr 6	NC_000006.11:g.154340898_154340900del
GRCh37.p13 chr 6	NC_000006.11:g.154340899_154340900del
GRCh37.p13 chr 6	NC_000006.11:g.154340900del
GRCh37.p13 chr 6	NC_000006.11:g.154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340899_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340898_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340897_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340896_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340895_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340894_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340893_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340892_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340891_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340890_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340889_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340887_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340886_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340885_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340884_154340900dup
GRCh37.p13 chr 6	NC_000006.11:g.154340900_154340901insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.154340900_154340901insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.154340900_154340901insTTTTTTTTTTTTTTTTTTTTTT
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14257_14265del
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14261_14265del
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14262_14265del
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14263_14265del
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14264_14265del
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14265del
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14264_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14263_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14262_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14261_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14260_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14259_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14258_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14257_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14256_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14255_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14254_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14252_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14251_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14250_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14249_14265dup
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14265_14266insTTTTTTTTTTTTTTTTTTTT
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14265_14266insTTTTTTTTTTTTTTTTTTTTT
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14265_14266insTTTTTTTTTTTTTTTTTTTTTT

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

Molecule type	Change	Amino acid[Codon]	SO Term
OPRM1 transcript variant MOR-1i	NM_001145279.4:c.-1+8739_… NM_001145279.4:c.-1+8739_-1+8747del	N/A	Intron Variant
OPRM1 transcript variant MOR-1G1	NM_001145280.4:c.-11+8739… NM_001145280.4:c.-11+8739_-11+8747del	N/A	Intron Variant
OPRM1 transcript variant MOR-1G2	NM_001145281.3:c.47+9198_… NM_001145281.3:c.47+9198_47+9206del	N/A	Intron Variant
OPRM1 transcript variant MOR-1	NM_000914.5:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1O	NM_001008503.3:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1A	NM_001008504.4:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1X	NM_001008505.2:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1B1	NM_001145282.2:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1B2	NM_001145283.2:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1B3	NM_001145284.3:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1B4	NM_001145285.3:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1B5	NM_001145286.3:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1K1	NM_001145287.3:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1S	NM_001285522.1:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1A2	NM_001285523.3:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1CA	NM_001285524.1:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1K2	NM_001285526.2:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1W	NM_001285527.1:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-3	NM_001285528.2:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1Y3	NR_104348.1:n.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1Y2	NR_104349.1:n.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1Z	NR_104350.1:n.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant MOR-1Y	NR_104351.1:n.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant X2	XM_011535851.4:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant X3	XM_011535853.3:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant X5	XM_011535856.3:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant X7	XM_011535862.3:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant X1	XM_017010903.3:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant X4	XM_017010904.2:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant X8	XM_017010907.3:c.	N/A	Genic Upstream Transcript Variant
OPRM1 transcript variant X6	XM_047418837.1:c.	N/A	Genic Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₁₈=	del(T)₉	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₄	dup(T)₁₅	dup(T)₁₆	dup(T)₁₇	ins(T)₂₀	ins(T)₂₁	ins(T)₂₂
GRCh38.p14 chr 6	NC_000006.12:g.154019748_154019765=	NC_000006.12:g.154019757_154019765del	NC_000006.12:g.154019761_154019765del	NC_000006.12:g.154019762_154019765del	NC_000006.12:g.154019763_154019765del	NC_000006.12:g.154019764_154019765del	NC_000006.12:g.154019765del	NC_000006.12:g.154019765dup	NC_000006.12:g.154019764_154019765dup	NC_000006.12:g.154019763_154019765dup	NC_000006.12:g.154019762_154019765dup	NC_000006.12:g.154019761_154019765dup	NC_000006.12:g.154019760_154019765dup	NC_000006.12:g.154019759_154019765dup	NC_000006.12:g.154019758_154019765dup	NC_000006.12:g.154019757_154019765dup	NC_000006.12:g.154019756_154019765dup	NC_000006.12:g.154019755_154019765dup	NC_000006.12:g.154019754_154019765dup	NC_000006.12:g.154019752_154019765dup	NC_000006.12:g.154019751_154019765dup	NC_000006.12:g.154019750_154019765dup	NC_000006.12:g.154019749_154019765dup	NC_000006.12:g.154019765_154019766insTTTTTTTTTTTTTTTTTTTT	NC_000006.12:g.154019765_154019766insTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:g.154019765_154019766insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.154340883_154340900=	NC_000006.11:g.154340892_154340900del	NC_000006.11:g.154340896_154340900del	NC_000006.11:g.154340897_154340900del	NC_000006.11:g.154340898_154340900del	NC_000006.11:g.154340899_154340900del	NC_000006.11:g.154340900del	NC_000006.11:g.154340900dup	NC_000006.11:g.154340899_154340900dup	NC_000006.11:g.154340898_154340900dup	NC_000006.11:g.154340897_154340900dup	NC_000006.11:g.154340896_154340900dup	NC_000006.11:g.154340895_154340900dup	NC_000006.11:g.154340894_154340900dup	NC_000006.11:g.154340893_154340900dup	NC_000006.11:g.154340892_154340900dup	NC_000006.11:g.154340891_154340900dup	NC_000006.11:g.154340890_154340900dup	NC_000006.11:g.154340889_154340900dup	NC_000006.11:g.154340887_154340900dup	NC_000006.11:g.154340886_154340900dup	NC_000006.11:g.154340885_154340900dup	NC_000006.11:g.154340884_154340900dup	NC_000006.11:g.154340900_154340901insTTTTTTTTTTTTTTTTTTTT	NC_000006.11:g.154340900_154340901insTTTTTTTTTTTTTTTTTTTTT	NC_000006.11:g.154340900_154340901insTTTTTTTTTTTTTTTTTTTTTT
OPRM1 RefSeqGene (LRG_1007)	NG_021208.2:g.14248_14265=	NG_021208.2:g.14257_14265del	NG_021208.2:g.14261_14265del	NG_021208.2:g.14262_14265del	NG_021208.2:g.14263_14265del	NG_021208.2:g.14264_14265del	NG_021208.2:g.14265del	NG_021208.2:g.14265dup	NG_021208.2:g.14264_14265dup	NG_021208.2:g.14263_14265dup	NG_021208.2:g.14262_14265dup	NG_021208.2:g.14261_14265dup	NG_021208.2:g.14260_14265dup	NG_021208.2:g.14259_14265dup	NG_021208.2:g.14258_14265dup	NG_021208.2:g.14257_14265dup	NG_021208.2:g.14256_14265dup	NG_021208.2:g.14255_14265dup	NG_021208.2:g.14254_14265dup	NG_021208.2:g.14252_14265dup	NG_021208.2:g.14251_14265dup	NG_021208.2:g.14250_14265dup	NG_021208.2:g.14249_14265dup	NG_021208.2:g.14265_14266insTTTTTTTTTTTTTTTTTTTT	NG_021208.2:g.14265_14266insTTTTTTTTTTTTTTTTTTTTT	NG_021208.2:g.14265_14266insTTTTTTTTTTTTTTTTTTTTTT
OPRM1 transcript variant MOR-1H	NM_001145279.2:c.-1+8730=	NM_001145279.2:c.-1+8739_-1+8747del	NM_001145279.2:c.-1+8743_-1+8747del	NM_001145279.2:c.-1+8744_-1+8747del	NM_001145279.2:c.-1+8745_-1+8747del	NM_001145279.2:c.-1+8746_-1+8747del	NM_001145279.2:c.-1+8747del	NM_001145279.2:c.-1+8747dup	NM_001145279.2:c.-1+8746_-1+8747dup	NM_001145279.2:c.-1+8745_-1+8747dup	NM_001145279.2:c.-1+8744_-1+8747dup	NM_001145279.2:c.-1+8743_-1+8747dup	NM_001145279.2:c.-1+8742_-1+8747dup	NM_001145279.2:c.-1+8741_-1+8747dup	NM_001145279.2:c.-1+8740_-1+8747dup	NM_001145279.2:c.-1+8739_-1+8747dup	NM_001145279.2:c.-1+8738_-1+8747dup	NM_001145279.2:c.-1+8737_-1+8747dup	NM_001145279.2:c.-1+8736_-1+8747dup	NM_001145279.2:c.-1+8734_-1+8747dup	NM_001145279.2:c.-1+8733_-1+8747dup	NM_001145279.2:c.-1+8732_-1+8747dup	NM_001145279.2:c.-1+8731_-1+8747dup	NM_001145279.2:c.-1+8747_-1+8748insTTTTTTTTTTTTTTTTTTTT	NM_001145279.2:c.-1+8747_-1+8748insTTTTTTTTTTTTTTTTTTTTT	NM_001145279.2:c.-1+8747_-1+8748insTTTTTTTTTTTTTTTTTTTTTT
OPRM1 transcript variant MOR-1i	NM_001145279.4:c.-1+8730=	NM_001145279.4:c.-1+8739_-1+8747del	NM_001145279.4:c.-1+8743_-1+8747del	NM_001145279.4:c.-1+8744_-1+8747del	NM_001145279.4:c.-1+8745_-1+8747del	NM_001145279.4:c.-1+8746_-1+8747del	NM_001145279.4:c.-1+8747del	NM_001145279.4:c.-1+8747dup	NM_001145279.4:c.-1+8746_-1+8747dup	NM_001145279.4:c.-1+8745_-1+8747dup	NM_001145279.4:c.-1+8744_-1+8747dup	NM_001145279.4:c.-1+8743_-1+8747dup	NM_001145279.4:c.-1+8742_-1+8747dup	NM_001145279.4:c.-1+8741_-1+8747dup	NM_001145279.4:c.-1+8740_-1+8747dup	NM_001145279.4:c.-1+8739_-1+8747dup	NM_001145279.4:c.-1+8738_-1+8747dup	NM_001145279.4:c.-1+8737_-1+8747dup	NM_001145279.4:c.-1+8736_-1+8747dup	NM_001145279.4:c.-1+8734_-1+8747dup	NM_001145279.4:c.-1+8733_-1+8747dup	NM_001145279.4:c.-1+8732_-1+8747dup	NM_001145279.4:c.-1+8731_-1+8747dup	NM_001145279.4:c.-1+8747_-1+8748insTTTTTTTTTTTTTTTTTTTT	NM_001145279.4:c.-1+8747_-1+8748insTTTTTTTTTTTTTTTTTTTTT	NM_001145279.4:c.-1+8747_-1+8748insTTTTTTTTTTTTTTTTTTTTTT
OPRM1 transcript variant MOR-1G1	NM_001145280.2:c.-11+8730=	NM_001145280.2:c.-11+8739_-11+8747del	NM_001145280.2:c.-11+8743_-11+8747del	NM_001145280.2:c.-11+8744_-11+8747del	NM_001145280.2:c.-11+8745_-11+8747del	NM_001145280.2:c.-11+8746_-11+8747del	NM_001145280.2:c.-11+8747del	NM_001145280.2:c.-11+8747dup	NM_001145280.2:c.-11+8746_-11+8747dup	NM_001145280.2:c.-11+8745_-11+8747dup	NM_001145280.2:c.-11+8744_-11+8747dup	NM_001145280.2:c.-11+8743_-11+8747dup	NM_001145280.2:c.-11+8742_-11+8747dup	NM_001145280.2:c.-11+8741_-11+8747dup	NM_001145280.2:c.-11+8740_-11+8747dup	NM_001145280.2:c.-11+8739_-11+8747dup	NM_001145280.2:c.-11+8738_-11+8747dup	NM_001145280.2:c.-11+8737_-11+8747dup	NM_001145280.2:c.-11+8736_-11+8747dup	NM_001145280.2:c.-11+8734_-11+8747dup	NM_001145280.2:c.-11+8733_-11+8747dup	NM_001145280.2:c.-11+8732_-11+8747dup	NM_001145280.2:c.-11+8731_-11+8747dup	NM_001145280.2:c.-11+8747_-11+8748insTTTTTTTTTTTTTTTTTTTT	NM_001145280.2:c.-11+8747_-11+8748insTTTTTTTTTTTTTTTTTTTTT	NM_001145280.2:c.-11+8747_-11+8748insTTTTTTTTTTTTTTTTTTTTTT
OPRM1 transcript variant MOR-1G1	NM_001145280.4:c.-11+8730=	NM_001145280.4:c.-11+8739_-11+8747del	NM_001145280.4:c.-11+8743_-11+8747del	NM_001145280.4:c.-11+8744_-11+8747del	NM_001145280.4:c.-11+8745_-11+8747del	NM_001145280.4:c.-11+8746_-11+8747del	NM_001145280.4:c.-11+8747del	NM_001145280.4:c.-11+8747dup	NM_001145280.4:c.-11+8746_-11+8747dup	NM_001145280.4:c.-11+8745_-11+8747dup	NM_001145280.4:c.-11+8744_-11+8747dup	NM_001145280.4:c.-11+8743_-11+8747dup	NM_001145280.4:c.-11+8742_-11+8747dup	NM_001145280.4:c.-11+8741_-11+8747dup	NM_001145280.4:c.-11+8740_-11+8747dup	NM_001145280.4:c.-11+8739_-11+8747dup	NM_001145280.4:c.-11+8738_-11+8747dup	NM_001145280.4:c.-11+8737_-11+8747dup	NM_001145280.4:c.-11+8736_-11+8747dup	NM_001145280.4:c.-11+8734_-11+8747dup	NM_001145280.4:c.-11+8733_-11+8747dup	NM_001145280.4:c.-11+8732_-11+8747dup	NM_001145280.4:c.-11+8731_-11+8747dup	NM_001145280.4:c.-11+8747_-11+8748insTTTTTTTTTTTTTTTTTTTT	NM_001145280.4:c.-11+8747_-11+8748insTTTTTTTTTTTTTTTTTTTTT	NM_001145280.4:c.-11+8747_-11+8748insTTTTTTTTTTTTTTTTTTTTTT
OPRM1 transcript variant MOR-1G2	NM_001145281.1:c.47+9189=	NM_001145281.1:c.47+9198_47+9206del	NM_001145281.1:c.47+9202_47+9206del	NM_001145281.1:c.47+9203_47+9206del	NM_001145281.1:c.47+9204_47+9206del	NM_001145281.1:c.47+9205_47+9206del	NM_001145281.1:c.47+9206del	NM_001145281.1:c.47+9206dup	NM_001145281.1:c.47+9205_47+9206dup	NM_001145281.1:c.47+9204_47+9206dup	NM_001145281.1:c.47+9203_47+9206dup	NM_001145281.1:c.47+9202_47+9206dup	NM_001145281.1:c.47+9201_47+9206dup	NM_001145281.1:c.47+9200_47+9206dup	NM_001145281.1:c.47+9199_47+9206dup	NM_001145281.1:c.47+9198_47+9206dup	NM_001145281.1:c.47+9197_47+9206dup	NM_001145281.1:c.47+9196_47+9206dup	NM_001145281.1:c.47+9195_47+9206dup	NM_001145281.1:c.47+9193_47+9206dup	NM_001145281.1:c.47+9192_47+9206dup	NM_001145281.1:c.47+9191_47+9206dup	NM_001145281.1:c.47+9190_47+9206dup	NM_001145281.1:c.47+9206_47+9207insTTTTTTTTTTTTTTTTTTTT	NM_001145281.1:c.47+9206_47+9207insTTTTTTTTTTTTTTTTTTTTT	NM_001145281.1:c.47+9206_47+9207insTTTTTTTTTTTTTTTTTTTTTT
OPRM1 transcript variant MOR-1G2	NM_001145281.3:c.47+9189=	NM_001145281.3:c.47+9198_47+9206del	NM_001145281.3:c.47+9202_47+9206del	NM_001145281.3:c.47+9203_47+9206del	NM_001145281.3:c.47+9204_47+9206del	NM_001145281.3:c.47+9205_47+9206del	NM_001145281.3:c.47+9206del	NM_001145281.3:c.47+9206dup	NM_001145281.3:c.47+9205_47+9206dup	NM_001145281.3:c.47+9204_47+9206dup	NM_001145281.3:c.47+9203_47+9206dup	NM_001145281.3:c.47+9202_47+9206dup	NM_001145281.3:c.47+9201_47+9206dup	NM_001145281.3:c.47+9200_47+9206dup	NM_001145281.3:c.47+9199_47+9206dup	NM_001145281.3:c.47+9198_47+9206dup	NM_001145281.3:c.47+9197_47+9206dup	NM_001145281.3:c.47+9196_47+9206dup	NM_001145281.3:c.47+9195_47+9206dup	NM_001145281.3:c.47+9193_47+9206dup	NM_001145281.3:c.47+9192_47+9206dup	NM_001145281.3:c.47+9191_47+9206dup	NM_001145281.3:c.47+9190_47+9206dup	NM_001145281.3:c.47+9206_47+9207insTTTTTTTTTTTTTTTTTTTT	NM_001145281.3:c.47+9206_47+9207insTTTTTTTTTTTTTTTTTTTTT	NM_001145281.3:c.47+9206_47+9207insTTTTTTTTTTTTTTTTTTTTTT

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#.

39 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSMP	ss663666810	Apr 01, 2015 (144)
2	BILGI_BIOE	ss666379723	Apr 25, 2013 (138)
3	SWEGEN	ss3000222326	Nov 08, 2017 (151)
4	PACBIO	ss3785665290	Jul 13, 2019 (153)
5	GNOMAD	ss4154384683	Apr 26, 2021 (155)
6	GNOMAD	ss4154384684	Apr 26, 2021 (155)
7	GNOMAD	ss4154384685	Apr 26, 2021 (155)
8	GNOMAD	ss4154384686	Apr 26, 2021 (155)
9	GNOMAD	ss4154384716	Apr 26, 2021 (155)
10	GNOMAD	ss4154384717	Apr 26, 2021 (155)
11	GNOMAD	ss4154384718	Apr 26, 2021 (155)
12	GNOMAD	ss4154384719	Apr 26, 2021 (155)
13	GNOMAD	ss4154384720	Apr 26, 2021 (155)
14	GNOMAD	ss4154384721	Apr 26, 2021 (155)
15	GNOMAD	ss4154384722	Apr 26, 2021 (155)
16	GNOMAD	ss4154384723	Apr 26, 2021 (155)
17	GNOMAD	ss4154384724	Apr 26, 2021 (155)
18	GNOMAD	ss4154384725	Apr 26, 2021 (155)
19	GNOMAD	ss4154384726	Apr 26, 2021 (155)
20	GNOMAD	ss4154384727	Apr 26, 2021 (155)
21	GNOMAD	ss4154384728	Apr 26, 2021 (155)
22	GNOMAD	ss4154384729	Apr 26, 2021 (155)
23	GNOMAD	ss4154384730	Apr 26, 2021 (155)
24	GNOMAD	ss4154384731	Apr 26, 2021 (155)
25	GNOMAD	ss4154384732	Apr 26, 2021 (155)
26	GNOMAD	ss4154384733	Apr 26, 2021 (155)
27	GNOMAD	ss4154384734	Apr 26, 2021 (155)
28	GNOMAD	ss4154384735	Apr 26, 2021 (155)
29	TOPMED	ss4727761103	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5180694114	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5180694115	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5180694117	Apr 26, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5270953595	Oct 14, 2022 (156)
34	HUGCELL_USP	ss5468343869	Oct 14, 2022 (156)
35	HUGCELL_USP	ss5468343870	Oct 14, 2022 (156)
36	TOMMO_GENOMICS	ss5719794249	Oct 14, 2022 (156)
37	TOMMO_GENOMICS	ss5719794250	Oct 14, 2022 (156)
38	TOMMO_GENOMICS	ss5719794251	Oct 14, 2022 (156)
39	TOMMO_GENOMICS	ss5719794253	Oct 14, 2022 (156)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 246079845 (NC_000006.12:154019747::T 2247/111776) Row 246079846 (NC_000006.12:154019747::TT 56/111786) Row 246079847 (NC_000006.12:154019747::TTT 2/111794)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 38663421 (NC_000006.11:154340882::T 773/16716) Row 38663422 (NC_000006.11:154340882::TTTTTT 25/16716) Row 38663424 (NC_000006.11:154340882:T: 22/16716)	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 38663421 (NC_000006.11:154340882::T 773/16716) Row 38663422 (NC_000006.11:154340882::TTTTTT 25/16716) Row 38663424 (NC_000006.11:154340882:T: 22/16716)	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 38663421 (NC_000006.11:154340882::T 773/16716) Row 38663422 (NC_000006.11:154340882::TTTTTT 25/16716) Row 38663424 (NC_000006.11:154340882:T: 22/16716)	-	Apr 26, 2021 (155)
67	14KJPN Submission ignored due to conflicting rows: Row 53631353 (NC_000006.12:154019747::T 1226/27748) Row 53631354 (NC_000006.12:154019747:TTTT: 11/27748) Row 53631355 (NC_000006.12:154019747::TTTTTT 53/27748)...	-	Oct 14, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 53631353 (NC_000006.12:154019747::T 1226/27748) Row 53631354 (NC_000006.12:154019747:TTTT: 11/27748) Row 53631355 (NC_000006.12:154019747::TTTTTT 53/27748)...	-	Oct 14, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 53631353 (NC_000006.12:154019747::T 1226/27748) Row 53631354 (NC_000006.12:154019747:TTTT: 11/27748) Row 53631355 (NC_000006.12:154019747::TTTTTT 53/27748)...	-	Oct 14, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 53631353 (NC_000006.12:154019747::T 1226/27748) Row 53631354 (NC_000006.12:154019747:TTTT: 11/27748) Row 53631355 (NC_000006.12:154019747::TTTTTT 53/27748)...	-	Oct 14, 2022 (156)
71	TopMed	NC_000006.12 - 154019748	Apr 26, 2021 (155)
72	ALFA	NC_000006.12 - 154019748	Apr 26, 2021 (155)

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

Associated ID	History Updated (Build)
rs377754773	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
565138661, ss4154384735, ss4727761103	NC_000006.12:154019747:TTTTTTTTT:	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4154384734	NC_000006.12:154019747:TTTTT:	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4154384733, ss5719794250	NC_000006.12:154019747:TTTT:	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4154384732	NC_000006.12:154019747:TTT:	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4154384731	NC_000006.12:154019747:TT:	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3000222326, ss3785665290, ss5180694117	NC_000006.11:154340882:T:	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4154384730, ss5468343869, ss5719794253	NC_000006.12:154019747:T:	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss663666810, ss666379723, ss5180694114	NC_000006.11:154340882::T	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4154384683, ss5270953595, ss5468343870, ss5719794249	NC_000006.12:154019747::T	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4154384684	NC_000006.12:154019747::TT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4154384685	NC_000006.12:154019747::TTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384686	NC_000006.12:154019747::TTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5180694115	NC_000006.11:154340882::TTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384716, ss5719794251	NC_000006.12:154019747::TTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384717	NC_000006.12:154019747::TTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384718	NC_000006.12:154019747::TTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384719	NC_000006.12:154019747::TTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384720	NC_000006.12:154019747::TTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384721	NC_000006.12:154019747::TTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384722	NC_000006.12:154019747::TTTTTTTTTT… NC_000006.12:154019747::TTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384723	NC_000006.12:154019747::TTTTTTTTTT… NC_000006.12:154019747::TTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384724	NC_000006.12:154019747::TTTTTTTTTT… NC_000006.12:154019747::TTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9695944974	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384725	NC_000006.12:154019747::TTTTTTTTTT… NC_000006.12:154019747::TTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384726	NC_000006.12:154019747::TTTTTTTTTT… NC_000006.12:154019747::TTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384727	NC_000006.12:154019747::TTTTTTTTTT… NC_000006.12:154019747::TTTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384728	NC_000006.12:154019747::TTTTTTTTTT… NC_000006.12:154019747::TTTTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154384729	NC_000006.12:154019747::TTTTTTTTTT… NC_000006.12:154019747::TTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3516351334	NC_000006.12:154019747::TTTTT	NC_000006.12:154019747:TTTTTTTTTTT… NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT

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

No publications for rs373120574

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs373120574