Name: rs34220070
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.

rs34220070

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:84068785-84068808 (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)₁₄ / del(T)₁₃ / del(T)₁₂ / d…
del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / insTCATCCACCCATATCA(T)₂₈ / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.03253 (360/11067, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MRAP2 : 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	11067	TTTTTTTTTTTTTTTTTTTTTTTT=0.94660	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00027, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.03253, TTTTTTTTTTTTTTTTTTTTTTT=0.00858, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00497, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00705, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.937156	0.001899	0.060946	3
European	Sub	9477	TTTTTTTTTTTTTTTTTTTTTTTT=0.9378	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0003, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0379, TTTTTTTTTTTTTTTTTTTTTTT=0.0099, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0058, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0082, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.926224	0.002236	0.07154	1
African	Sub	760	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	24	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	736	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	64	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	52	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	64	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	388	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	46	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	268	TTTTTTTTTTTTTTTTTTTTTTTT=0.993	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.004, TTTTTTTTTTTTTTTTTTTTTTT=0.004, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.992481	0.0	0.007519	0

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	11067	(T)₂₄=0.94660	del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00027, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.03253, delT=0.00858, dupT=0.00497, dupTT=0.00705, dupTTT=0.00000, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	9477	(T)₂₄=0.9378	del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0003, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0379, delT=0.0099, dupT=0.0058, dupTT=0.0082, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	760	(T)₂₄=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	388	(T)₂₄=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	268	(T)₂₄=0.993	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.004, delT=0.004, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	64	(T)₂₄=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	64	(T)₂₄=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	46	(T)₂₄=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=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.84068795_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068796_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068797_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068798_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068799_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068800_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068801_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068802_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068803_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068804_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068805_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068806_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068807_84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068808del
GRCh38.p14 chr 6	NC_000006.12:g.84068808dup
GRCh38.p14 chr 6	NC_000006.12:g.84068785_84068808T[25]CATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 6	NC_000006.12:g.84068807_84068808dup
GRCh38.p14 chr 6	NC_000006.12:g.84068806_84068808dup
GRCh38.p14 chr 6	NC_000006.12:g.84068805_84068808dup
GRCh38.p14 chr 6	NC_000006.12:g.84068804_84068808dup
GRCh38.p14 chr 6	NC_000006.12:g.84068803_84068808dup
GRCh38.p14 chr 6	NC_000006.12:g.84068802_84068808dup
GRCh38.p14 chr 6	NC_000006.12:g.84068801_84068808dup
GRCh38.p14 chr 6	NC_000006.12:g.84068800_84068808dup
GRCh37.p13 chr 6	NC_000006.11:g.84778514_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778515_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778516_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778517_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778518_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778519_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778520_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778521_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778522_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778523_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778524_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778525_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778526_84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778527del
GRCh37.p13 chr 6	NC_000006.11:g.84778527dup
GRCh37.p13 chr 6	NC_000006.11:g.84778504_84778527T[25]CATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 6	NC_000006.11:g.84778526_84778527dup
GRCh37.p13 chr 6	NC_000006.11:g.84778525_84778527dup
GRCh37.p13 chr 6	NC_000006.11:g.84778524_84778527dup
GRCh37.p13 chr 6	NC_000006.11:g.84778523_84778527dup
GRCh37.p13 chr 6	NC_000006.11:g.84778522_84778527dup
GRCh37.p13 chr 6	NC_000006.11:g.84778521_84778527dup
GRCh37.p13 chr 6	NC_000006.11:g.84778520_84778527dup
GRCh37.p13 chr 6	NC_000006.11:g.84778519_84778527dup
MRAP2 RefSeqGene	NG_051944.1:g.40137_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40138_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40139_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40140_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40141_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40142_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40143_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40144_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40145_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40146_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40147_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40148_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40149_40150del
MRAP2 RefSeqGene	NG_051944.1:g.40150del
MRAP2 RefSeqGene	NG_051944.1:g.40150dup
MRAP2 RefSeqGene	NG_051944.1:g.40127_40150T[25]CATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
MRAP2 RefSeqGene	NG_051944.1:g.40149_40150dup
MRAP2 RefSeqGene	NG_051944.1:g.40148_40150dup
MRAP2 RefSeqGene	NG_051944.1:g.40147_40150dup
MRAP2 RefSeqGene	NG_051944.1:g.40146_40150dup
MRAP2 RefSeqGene	NG_051944.1:g.40145_40150dup
MRAP2 RefSeqGene	NG_051944.1:g.40144_40150dup
MRAP2 RefSeqGene	NG_051944.1:g.40143_40150dup
MRAP2 RefSeqGene	NG_051944.1:g.40142_40150dup

Gene: MRAP2, melanocortin 2 receptor accessory protein 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MRAP2 transcript variant 2	NM_001346541.2:c.-32+1335… NM_001346541.2:c.-32+13350_-32+13363del	N/A	Intron Variant
MRAP2 transcript variant 3	NM_001346542.2:c.227+5803… NM_001346542.2:c.227+5803_227+5816del	N/A	Intron Variant
MRAP2 transcript variant 4	NM_001346543.2:c.-33+5803… NM_001346543.2:c.-33+5803_-33+5816del	N/A	Intron Variant
MRAP2 transcript variant 5	NM_001346544.2:c.227+5803… NM_001346544.2:c.227+5803_227+5816del	N/A	Intron Variant
MRAP2 transcript variant 1	NM_138409.4:c.227+5803_22… NM_138409.4:c.227+5803_227+5816del	N/A	Intron Variant
MRAP2 transcript variant X2	XM_017010220.2:c.227+5803… XM_017010220.2:c.227+5803_227+5816del	N/A	Intron Variant
MRAP2 transcript variant X3	XM_017010221.3:c.227+5803… XM_017010221.3:c.227+5803_227+5816del	N/A	Intron Variant
MRAP2 transcript variant X1	XM_047418132.1:c.227+5803… XM_047418132.1:c.227+5803_227+5816del	N/A	Intron Variant
MRAP2 transcript variant X4	XM_047418133.1:c.-32+2057… XM_047418133.1:c.-32+2057_-32+2070del	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₄=	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	insTCATCCACCCATATCA(T)₂₈	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉
GRCh38.p14 chr 6	NC_000006.12:g.84068785_84068808=	NC_000006.12:g.84068795_84068808del	NC_000006.12:g.84068796_84068808del	NC_000006.12:g.84068797_84068808del	NC_000006.12:g.84068798_84068808del	NC_000006.12:g.84068799_84068808del	NC_000006.12:g.84068800_84068808del	NC_000006.12:g.84068801_84068808del	NC_000006.12:g.84068802_84068808del	NC_000006.12:g.84068803_84068808del	NC_000006.12:g.84068804_84068808del	NC_000006.12:g.84068805_84068808del	NC_000006.12:g.84068806_84068808del	NC_000006.12:g.84068807_84068808del	NC_000006.12:g.84068808del	NC_000006.12:g.84068808dup	NC_000006.12:g.84068785_84068808T[25]CATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000006.12:g.84068807_84068808dup	NC_000006.12:g.84068806_84068808dup	NC_000006.12:g.84068805_84068808dup	NC_000006.12:g.84068804_84068808dup	NC_000006.12:g.84068803_84068808dup	NC_000006.12:g.84068802_84068808dup	NC_000006.12:g.84068801_84068808dup	NC_000006.12:g.84068800_84068808dup
GRCh37.p13 chr 6	NC_000006.11:g.84778504_84778527=	NC_000006.11:g.84778514_84778527del	NC_000006.11:g.84778515_84778527del	NC_000006.11:g.84778516_84778527del	NC_000006.11:g.84778517_84778527del	NC_000006.11:g.84778518_84778527del	NC_000006.11:g.84778519_84778527del	NC_000006.11:g.84778520_84778527del	NC_000006.11:g.84778521_84778527del	NC_000006.11:g.84778522_84778527del	NC_000006.11:g.84778523_84778527del	NC_000006.11:g.84778524_84778527del	NC_000006.11:g.84778525_84778527del	NC_000006.11:g.84778526_84778527del	NC_000006.11:g.84778527del	NC_000006.11:g.84778527dup	NC_000006.11:g.84778504_84778527T[25]CATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000006.11:g.84778526_84778527dup	NC_000006.11:g.84778525_84778527dup	NC_000006.11:g.84778524_84778527dup	NC_000006.11:g.84778523_84778527dup	NC_000006.11:g.84778522_84778527dup	NC_000006.11:g.84778521_84778527dup	NC_000006.11:g.84778520_84778527dup	NC_000006.11:g.84778519_84778527dup
MRAP2 RefSeqGene	NG_051944.1:g.40127_40150=	NG_051944.1:g.40137_40150del	NG_051944.1:g.40138_40150del	NG_051944.1:g.40139_40150del	NG_051944.1:g.40140_40150del	NG_051944.1:g.40141_40150del	NG_051944.1:g.40142_40150del	NG_051944.1:g.40143_40150del	NG_051944.1:g.40144_40150del	NG_051944.1:g.40145_40150del	NG_051944.1:g.40146_40150del	NG_051944.1:g.40147_40150del	NG_051944.1:g.40148_40150del	NG_051944.1:g.40149_40150del	NG_051944.1:g.40150del	NG_051944.1:g.40150dup	NG_051944.1:g.40127_40150T[25]CATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NG_051944.1:g.40149_40150dup	NG_051944.1:g.40148_40150dup	NG_051944.1:g.40147_40150dup	NG_051944.1:g.40146_40150dup	NG_051944.1:g.40145_40150dup	NG_051944.1:g.40144_40150dup	NG_051944.1:g.40143_40150dup	NG_051944.1:g.40142_40150dup
MRAP2 transcript variant 2	NM_001346541.2:c.-32+13340=	NM_001346541.2:c.-32+13350_-32+13363del	NM_001346541.2:c.-32+13351_-32+13363del	NM_001346541.2:c.-32+13352_-32+13363del	NM_001346541.2:c.-32+13353_-32+13363del	NM_001346541.2:c.-32+13354_-32+13363del	NM_001346541.2:c.-32+13355_-32+13363del	NM_001346541.2:c.-32+13356_-32+13363del	NM_001346541.2:c.-32+13357_-32+13363del	NM_001346541.2:c.-32+13358_-32+13363del	NM_001346541.2:c.-32+13359_-32+13363del	NM_001346541.2:c.-32+13360_-32+13363del	NM_001346541.2:c.-32+13361_-32+13363del	NM_001346541.2:c.-32+13362_-32+13363del	NM_001346541.2:c.-32+13363del	NM_001346541.2:c.-32+13363dup	NM_001346541.2:c.-32+13363_-32+13364insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001346541.2:c.-32+13362_-32+13363dup	NM_001346541.2:c.-32+13361_-32+13363dup	NM_001346541.2:c.-32+13360_-32+13363dup	NM_001346541.2:c.-32+13359_-32+13363dup	NM_001346541.2:c.-32+13358_-32+13363dup	NM_001346541.2:c.-32+13357_-32+13363dup	NM_001346541.2:c.-32+13356_-32+13363dup	NM_001346541.2:c.-32+13355_-32+13363dup
MRAP2 transcript variant 3	NM_001346542.2:c.227+5793=	NM_001346542.2:c.227+5803_227+5816del	NM_001346542.2:c.227+5804_227+5816del	NM_001346542.2:c.227+5805_227+5816del	NM_001346542.2:c.227+5806_227+5816del	NM_001346542.2:c.227+5807_227+5816del	NM_001346542.2:c.227+5808_227+5816del	NM_001346542.2:c.227+5809_227+5816del	NM_001346542.2:c.227+5810_227+5816del	NM_001346542.2:c.227+5811_227+5816del	NM_001346542.2:c.227+5812_227+5816del	NM_001346542.2:c.227+5813_227+5816del	NM_001346542.2:c.227+5814_227+5816del	NM_001346542.2:c.227+5815_227+5816del	NM_001346542.2:c.227+5816del	NM_001346542.2:c.227+5816dup	NM_001346542.2:c.227+5816_227+5817insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001346542.2:c.227+5815_227+5816dup	NM_001346542.2:c.227+5814_227+5816dup	NM_001346542.2:c.227+5813_227+5816dup	NM_001346542.2:c.227+5812_227+5816dup	NM_001346542.2:c.227+5811_227+5816dup	NM_001346542.2:c.227+5810_227+5816dup	NM_001346542.2:c.227+5809_227+5816dup	NM_001346542.2:c.227+5808_227+5816dup
MRAP2 transcript variant 4	NM_001346543.2:c.-33+5793=	NM_001346543.2:c.-33+5803_-33+5816del	NM_001346543.2:c.-33+5804_-33+5816del	NM_001346543.2:c.-33+5805_-33+5816del	NM_001346543.2:c.-33+5806_-33+5816del	NM_001346543.2:c.-33+5807_-33+5816del	NM_001346543.2:c.-33+5808_-33+5816del	NM_001346543.2:c.-33+5809_-33+5816del	NM_001346543.2:c.-33+5810_-33+5816del	NM_001346543.2:c.-33+5811_-33+5816del	NM_001346543.2:c.-33+5812_-33+5816del	NM_001346543.2:c.-33+5813_-33+5816del	NM_001346543.2:c.-33+5814_-33+5816del	NM_001346543.2:c.-33+5815_-33+5816del	NM_001346543.2:c.-33+5816del	NM_001346543.2:c.-33+5816dup	NM_001346543.2:c.-33+5816_-33+5817insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001346543.2:c.-33+5815_-33+5816dup	NM_001346543.2:c.-33+5814_-33+5816dup	NM_001346543.2:c.-33+5813_-33+5816dup	NM_001346543.2:c.-33+5812_-33+5816dup	NM_001346543.2:c.-33+5811_-33+5816dup	NM_001346543.2:c.-33+5810_-33+5816dup	NM_001346543.2:c.-33+5809_-33+5816dup	NM_001346543.2:c.-33+5808_-33+5816dup
MRAP2 transcript variant 5	NM_001346544.2:c.227+5793=	NM_001346544.2:c.227+5803_227+5816del	NM_001346544.2:c.227+5804_227+5816del	NM_001346544.2:c.227+5805_227+5816del	NM_001346544.2:c.227+5806_227+5816del	NM_001346544.2:c.227+5807_227+5816del	NM_001346544.2:c.227+5808_227+5816del	NM_001346544.2:c.227+5809_227+5816del	NM_001346544.2:c.227+5810_227+5816del	NM_001346544.2:c.227+5811_227+5816del	NM_001346544.2:c.227+5812_227+5816del	NM_001346544.2:c.227+5813_227+5816del	NM_001346544.2:c.227+5814_227+5816del	NM_001346544.2:c.227+5815_227+5816del	NM_001346544.2:c.227+5816del	NM_001346544.2:c.227+5816dup	NM_001346544.2:c.227+5816_227+5817insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001346544.2:c.227+5815_227+5816dup	NM_001346544.2:c.227+5814_227+5816dup	NM_001346544.2:c.227+5813_227+5816dup	NM_001346544.2:c.227+5812_227+5816dup	NM_001346544.2:c.227+5811_227+5816dup	NM_001346544.2:c.227+5810_227+5816dup	NM_001346544.2:c.227+5809_227+5816dup	NM_001346544.2:c.227+5808_227+5816dup
MRAP2 transcript	NM_138409.2:c.227+5793=	NM_138409.2:c.227+5803_227+5816del	NM_138409.2:c.227+5804_227+5816del	NM_138409.2:c.227+5805_227+5816del	NM_138409.2:c.227+5806_227+5816del	NM_138409.2:c.227+5807_227+5816del	NM_138409.2:c.227+5808_227+5816del	NM_138409.2:c.227+5809_227+5816del	NM_138409.2:c.227+5810_227+5816del	NM_138409.2:c.227+5811_227+5816del	NM_138409.2:c.227+5812_227+5816del	NM_138409.2:c.227+5813_227+5816del	NM_138409.2:c.227+5814_227+5816del	NM_138409.2:c.227+5815_227+5816del	NM_138409.2:c.227+5816del	NM_138409.2:c.227+5816dup	NM_138409.2:c.227+5816_227+5817insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_138409.2:c.227+5815_227+5816dup	NM_138409.2:c.227+5814_227+5816dup	NM_138409.2:c.227+5813_227+5816dup	NM_138409.2:c.227+5812_227+5816dup	NM_138409.2:c.227+5811_227+5816dup	NM_138409.2:c.227+5810_227+5816dup	NM_138409.2:c.227+5809_227+5816dup	NM_138409.2:c.227+5808_227+5816dup
MRAP2 transcript variant 1	NM_138409.4:c.227+5793=	NM_138409.4:c.227+5803_227+5816del	NM_138409.4:c.227+5804_227+5816del	NM_138409.4:c.227+5805_227+5816del	NM_138409.4:c.227+5806_227+5816del	NM_138409.4:c.227+5807_227+5816del	NM_138409.4:c.227+5808_227+5816del	NM_138409.4:c.227+5809_227+5816del	NM_138409.4:c.227+5810_227+5816del	NM_138409.4:c.227+5811_227+5816del	NM_138409.4:c.227+5812_227+5816del	NM_138409.4:c.227+5813_227+5816del	NM_138409.4:c.227+5814_227+5816del	NM_138409.4:c.227+5815_227+5816del	NM_138409.4:c.227+5816del	NM_138409.4:c.227+5816dup	NM_138409.4:c.227+5816_227+5817insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_138409.4:c.227+5815_227+5816dup	NM_138409.4:c.227+5814_227+5816dup	NM_138409.4:c.227+5813_227+5816dup	NM_138409.4:c.227+5812_227+5816dup	NM_138409.4:c.227+5811_227+5816dup	NM_138409.4:c.227+5810_227+5816dup	NM_138409.4:c.227+5809_227+5816dup	NM_138409.4:c.227+5808_227+5816dup
MRAP2 transcript variant X1	XM_005248644.1:c.227+5793=	XM_005248644.1:c.227+5803_227+5816del	XM_005248644.1:c.227+5804_227+5816del	XM_005248644.1:c.227+5805_227+5816del	XM_005248644.1:c.227+5806_227+5816del	XM_005248644.1:c.227+5807_227+5816del	XM_005248644.1:c.227+5808_227+5816del	XM_005248644.1:c.227+5809_227+5816del	XM_005248644.1:c.227+5810_227+5816del	XM_005248644.1:c.227+5811_227+5816del	XM_005248644.1:c.227+5812_227+5816del	XM_005248644.1:c.227+5813_227+5816del	XM_005248644.1:c.227+5814_227+5816del	XM_005248644.1:c.227+5815_227+5816del	XM_005248644.1:c.227+5816del	XM_005248644.1:c.227+5816dup	XM_005248644.1:c.227+5816_227+5817insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005248644.1:c.227+5815_227+5816dup	XM_005248644.1:c.227+5814_227+5816dup	XM_005248644.1:c.227+5813_227+5816dup	XM_005248644.1:c.227+5812_227+5816dup	XM_005248644.1:c.227+5811_227+5816dup	XM_005248644.1:c.227+5810_227+5816dup	XM_005248644.1:c.227+5809_227+5816dup	XM_005248644.1:c.227+5808_227+5816dup
MRAP2 transcript variant X2	XM_005248645.1:c.227+5793=	XM_005248645.1:c.227+5803_227+5816del	XM_005248645.1:c.227+5804_227+5816del	XM_005248645.1:c.227+5805_227+5816del	XM_005248645.1:c.227+5806_227+5816del	XM_005248645.1:c.227+5807_227+5816del	XM_005248645.1:c.227+5808_227+5816del	XM_005248645.1:c.227+5809_227+5816del	XM_005248645.1:c.227+5810_227+5816del	XM_005248645.1:c.227+5811_227+5816del	XM_005248645.1:c.227+5812_227+5816del	XM_005248645.1:c.227+5813_227+5816del	XM_005248645.1:c.227+5814_227+5816del	XM_005248645.1:c.227+5815_227+5816del	XM_005248645.1:c.227+5816del	XM_005248645.1:c.227+5816dup	XM_005248645.1:c.227+5816_227+5817insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005248645.1:c.227+5815_227+5816dup	XM_005248645.1:c.227+5814_227+5816dup	XM_005248645.1:c.227+5813_227+5816dup	XM_005248645.1:c.227+5812_227+5816dup	XM_005248645.1:c.227+5811_227+5816dup	XM_005248645.1:c.227+5810_227+5816dup	XM_005248645.1:c.227+5809_227+5816dup	XM_005248645.1:c.227+5808_227+5816dup
MRAP2 transcript variant X3	XM_005248646.1:c.227+5793=	XM_005248646.1:c.227+5803_227+5816del	XM_005248646.1:c.227+5804_227+5816del	XM_005248646.1:c.227+5805_227+5816del	XM_005248646.1:c.227+5806_227+5816del	XM_005248646.1:c.227+5807_227+5816del	XM_005248646.1:c.227+5808_227+5816del	XM_005248646.1:c.227+5809_227+5816del	XM_005248646.1:c.227+5810_227+5816del	XM_005248646.1:c.227+5811_227+5816del	XM_005248646.1:c.227+5812_227+5816del	XM_005248646.1:c.227+5813_227+5816del	XM_005248646.1:c.227+5814_227+5816del	XM_005248646.1:c.227+5815_227+5816del	XM_005248646.1:c.227+5816del	XM_005248646.1:c.227+5816dup	XM_005248646.1:c.227+5816_227+5817insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005248646.1:c.227+5815_227+5816dup	XM_005248646.1:c.227+5814_227+5816dup	XM_005248646.1:c.227+5813_227+5816dup	XM_005248646.1:c.227+5812_227+5816dup	XM_005248646.1:c.227+5811_227+5816dup	XM_005248646.1:c.227+5810_227+5816dup	XM_005248646.1:c.227+5809_227+5816dup	XM_005248646.1:c.227+5808_227+5816dup
MRAP2 transcript variant X2	XM_017010220.2:c.227+5793=	XM_017010220.2:c.227+5803_227+5816del	XM_017010220.2:c.227+5804_227+5816del	XM_017010220.2:c.227+5805_227+5816del	XM_017010220.2:c.227+5806_227+5816del	XM_017010220.2:c.227+5807_227+5816del	XM_017010220.2:c.227+5808_227+5816del	XM_017010220.2:c.227+5809_227+5816del	XM_017010220.2:c.227+5810_227+5816del	XM_017010220.2:c.227+5811_227+5816del	XM_017010220.2:c.227+5812_227+5816del	XM_017010220.2:c.227+5813_227+5816del	XM_017010220.2:c.227+5814_227+5816del	XM_017010220.2:c.227+5815_227+5816del	XM_017010220.2:c.227+5816del	XM_017010220.2:c.227+5816dup	XM_017010220.2:c.227+5816_227+5817insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017010220.2:c.227+5815_227+5816dup	XM_017010220.2:c.227+5814_227+5816dup	XM_017010220.2:c.227+5813_227+5816dup	XM_017010220.2:c.227+5812_227+5816dup	XM_017010220.2:c.227+5811_227+5816dup	XM_017010220.2:c.227+5810_227+5816dup	XM_017010220.2:c.227+5809_227+5816dup	XM_017010220.2:c.227+5808_227+5816dup
MRAP2 transcript variant X3	XM_017010221.3:c.227+5793=	XM_017010221.3:c.227+5803_227+5816del	XM_017010221.3:c.227+5804_227+5816del	XM_017010221.3:c.227+5805_227+5816del	XM_017010221.3:c.227+5806_227+5816del	XM_017010221.3:c.227+5807_227+5816del	XM_017010221.3:c.227+5808_227+5816del	XM_017010221.3:c.227+5809_227+5816del	XM_017010221.3:c.227+5810_227+5816del	XM_017010221.3:c.227+5811_227+5816del	XM_017010221.3:c.227+5812_227+5816del	XM_017010221.3:c.227+5813_227+5816del	XM_017010221.3:c.227+5814_227+5816del	XM_017010221.3:c.227+5815_227+5816del	XM_017010221.3:c.227+5816del	XM_017010221.3:c.227+5816dup	XM_017010221.3:c.227+5816_227+5817insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017010221.3:c.227+5815_227+5816dup	XM_017010221.3:c.227+5814_227+5816dup	XM_017010221.3:c.227+5813_227+5816dup	XM_017010221.3:c.227+5812_227+5816dup	XM_017010221.3:c.227+5811_227+5816dup	XM_017010221.3:c.227+5810_227+5816dup	XM_017010221.3:c.227+5809_227+5816dup	XM_017010221.3:c.227+5808_227+5816dup
MRAP2 transcript variant X1	XM_047418132.1:c.227+5793=	XM_047418132.1:c.227+5803_227+5816del	XM_047418132.1:c.227+5804_227+5816del	XM_047418132.1:c.227+5805_227+5816del	XM_047418132.1:c.227+5806_227+5816del	XM_047418132.1:c.227+5807_227+5816del	XM_047418132.1:c.227+5808_227+5816del	XM_047418132.1:c.227+5809_227+5816del	XM_047418132.1:c.227+5810_227+5816del	XM_047418132.1:c.227+5811_227+5816del	XM_047418132.1:c.227+5812_227+5816del	XM_047418132.1:c.227+5813_227+5816del	XM_047418132.1:c.227+5814_227+5816del	XM_047418132.1:c.227+5815_227+5816del	XM_047418132.1:c.227+5816del	XM_047418132.1:c.227+5816dup	XM_047418132.1:c.227+5816_227+5817insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047418132.1:c.227+5815_227+5816dup	XM_047418132.1:c.227+5814_227+5816dup	XM_047418132.1:c.227+5813_227+5816dup	XM_047418132.1:c.227+5812_227+5816dup	XM_047418132.1:c.227+5811_227+5816dup	XM_047418132.1:c.227+5810_227+5816dup	XM_047418132.1:c.227+5809_227+5816dup	XM_047418132.1:c.227+5808_227+5816dup
MRAP2 transcript variant X4	XM_047418133.1:c.-32+2047=	XM_047418133.1:c.-32+2057_-32+2070del	XM_047418133.1:c.-32+2058_-32+2070del	XM_047418133.1:c.-32+2059_-32+2070del	XM_047418133.1:c.-32+2060_-32+2070del	XM_047418133.1:c.-32+2061_-32+2070del	XM_047418133.1:c.-32+2062_-32+2070del	XM_047418133.1:c.-32+2063_-32+2070del	XM_047418133.1:c.-32+2064_-32+2070del	XM_047418133.1:c.-32+2065_-32+2070del	XM_047418133.1:c.-32+2066_-32+2070del	XM_047418133.1:c.-32+2067_-32+2070del	XM_047418133.1:c.-32+2068_-32+2070del	XM_047418133.1:c.-32+2069_-32+2070del	XM_047418133.1:c.-32+2070del	XM_047418133.1:c.-32+2070dup	XM_047418133.1:c.-32+2070_-32+2071insTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_047418133.1:c.-32+2069_-32+2070dup	XM_047418133.1:c.-32+2068_-32+2070dup	XM_047418133.1:c.-32+2067_-32+2070dup	XM_047418133.1:c.-32+2066_-32+2070dup	XM_047418133.1:c.-32+2065_-32+2070dup	XM_047418133.1:c.-32+2064_-32+2070dup	XM_047418133.1:c.-32+2063_-32+2070dup	XM_047418133.1:c.-32+2062_-32+2070dup

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#.

46 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42792003	Mar 13, 2006 (126)
2	HGSV	ss79818570	Dec 15, 2007 (130)
3	SWEGEN	ss2999454626	Jan 10, 2018 (151)
4	PACBIO	ss3785538012	Jul 13, 2019 (153)
5	PACBIO	ss3790879394	Jul 13, 2019 (153)
6	PACBIO	ss3790879395	Jul 13, 2019 (153)
7	PACBIO	ss3795758525	Jul 13, 2019 (153)
8	PACBIO	ss3795758526	Jul 13, 2019 (153)
9	GNOMAD	ss4145826633	Apr 27, 2021 (155)
10	GNOMAD	ss4145826634	Apr 27, 2021 (155)
11	GNOMAD	ss4145826635	Apr 27, 2021 (155)
12	GNOMAD	ss4145826636	Apr 27, 2021 (155)
13	GNOMAD	ss4145826637	Apr 27, 2021 (155)
14	GNOMAD	ss4145826638	Apr 27, 2021 (155)
15	GNOMAD	ss4145826639	Apr 27, 2021 (155)
16	GNOMAD	ss4145826640	Apr 27, 2021 (155)
17	GNOMAD	ss4145826641	Apr 27, 2021 (155)
18	GNOMAD	ss4145826642	Apr 27, 2021 (155)
19	GNOMAD	ss4145826643	Apr 27, 2021 (155)
20	GNOMAD	ss4145826644	Apr 27, 2021 (155)
21	GNOMAD	ss4145826645	Apr 27, 2021 (155)
22	GNOMAD	ss4145826646	Apr 27, 2021 (155)
23	GNOMAD	ss4145826647	Apr 27, 2021 (155)
24	GNOMAD	ss4145826648	Apr 27, 2021 (155)
25	GNOMAD	ss4145826649	Apr 27, 2021 (155)
26	GNOMAD	ss4145826650	Apr 27, 2021 (155)
27	TOPMED	ss4710922964	Apr 27, 2021 (155)
28	TOPMED	ss4710922965	Apr 27, 2021 (155)
29	TOMMO_GENOMICS	ss5178533811	Apr 27, 2021 (155)
30	TOMMO_GENOMICS	ss5178533812	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5178533813	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5178533814	Apr 27, 2021 (155)
33	TOMMO_GENOMICS	ss5178533815	Apr 27, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5269258942	Oct 13, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5269258943	Oct 13, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5269258944	Oct 13, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5269258945	Oct 13, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5269258946	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5466811051	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5466811052	Oct 13, 2022 (156)
41	HUGCELL_USP	ss5466811053	Oct 13, 2022 (156)
42	TOMMO_GENOMICS	ss5717011273	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5717011275	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5717011276	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5717011277	Oct 13, 2022 (156)
46	EVA	ss5855451389	Oct 13, 2022 (156)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 231925060 (NC_000006.12:84068784::T 1571/51690) Row 231925061 (NC_000006.12:84068784::TT 1562/51582) Row 231925062 (NC_000006.12:84068784::TTT 297/51682)...	-	Apr 27, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 36503118 (NC_000006.11:84778503:TT: 1297/16584) Row 36503119 (NC_000006.11:84778503::T 388/16584) Row 36503120 (NC_000006.11:84778503:T: 193/16584)...	-	Apr 27, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 36503118 (NC_000006.11:84778503:TT: 1297/16584) Row 36503119 (NC_000006.11:84778503::T 388/16584) Row 36503120 (NC_000006.11:84778503:T: 193/16584)...	-	Apr 27, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 36503118 (NC_000006.11:84778503:TT: 1297/16584) Row 36503119 (NC_000006.11:84778503::T 388/16584) Row 36503120 (NC_000006.11:84778503:T: 193/16584)...	-	Apr 27, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 36503118 (NC_000006.11:84778503:TT: 1297/16584) Row 36503119 (NC_000006.11:84778503::T 388/16584) Row 36503120 (NC_000006.11:84778503:T: 193/16584)...	-	Apr 27, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 36503118 (NC_000006.11:84778503:TT: 1297/16584) Row 36503119 (NC_000006.11:84778503::T 388/16584) Row 36503120 (NC_000006.11:84778503:T: 193/16584)...	-	Apr 27, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 50848377 (NC_000006.12:84068784:TT: 2068/25038) Row 50848379 (NC_000006.12:84068784::T 508/25038) Row 50848380 (NC_000006.12:84068784:T: 333/25038)...	-	Oct 13, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 50848377 (NC_000006.12:84068784:TT: 2068/25038) Row 50848379 (NC_000006.12:84068784::T 508/25038) Row 50848380 (NC_000006.12:84068784:T: 333/25038)...	-	Oct 13, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 50848377 (NC_000006.12:84068784:TT: 2068/25038) Row 50848379 (NC_000006.12:84068784::T 508/25038) Row 50848380 (NC_000006.12:84068784:T: 333/25038)...	-	Oct 13, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 50848377 (NC_000006.12:84068784:TT: 2068/25038) Row 50848379 (NC_000006.12:84068784::T 508/25038) Row 50848380 (NC_000006.12:84068784:T: 333/25038)...	-	Oct 13, 2022 (156)
74	TopMed Submission ignored due to conflicting rows: Row 548300522 (NC_000006.12:84068784:TTTTTTTTTTT: 2/264690) Row 548300523 (NC_000006.12:84068784:TTTTTTTTTTTT: 14/264690)	-	Apr 27, 2021 (155)
75	TopMed Submission ignored due to conflicting rows: Row 548300522 (NC_000006.12:84068784:TTTTTTTTTTT: 2/264690) Row 548300523 (NC_000006.12:84068784:TTTTTTTTTTTT: 14/264690)	-	Apr 27, 2021 (155)
76	ALFA	NC_000006.12 - 84068785	Apr 27, 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)
rs60270218	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4145826650, ss4710922965	NC_000006.12:84068784:TTTTTTTTTTTT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4710922964	NC_000006.12:84068784:TTTTTTTTTTT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4145826649	NC_000006.12:84068784:TTTTTTTT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4145826648	NC_000006.12:84068784:TTTTTTT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4145826647	NC_000006.12:84068784:TTTTTT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5178533814	NC_000006.11:84778503:TTTT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4145826646, ss5269258946	NC_000006.12:84068784:TTTT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3785538012	NC_000006.11:84778503:TTT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826645	NC_000006.12:84068784:TTT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss2999454626, ss3790879394, ss3795758525, ss5178533811	NC_000006.11:84778503:TT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826644, ss5269258944, ss5466811052, ss5717011273	NC_000006.12:84068784:TT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss79818570	NC_000006.9:84835245:T:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3790879395, ss3795758526, ss5178533813	NC_000006.11:84778503:T:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826643, ss5466811053, ss5717011276	NC_000006.12:84068784:T:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss42792003	NT_007299.13:22898360:T:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5178533812	NC_000006.11:84778503::T	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826633, ss5269258942, ss5466811051, ss5717011275, ss5855451389	NC_000006.12:84068784::T	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826642	NC_000006.12:84068784::TTTTTTTTTTT… NC_000006.12:84068784::TTTTTTTTTTTTTTTTTTTTTTTTTCATCCACCCATATCATTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTCATCCACCCATATCATTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5178533815	NC_000006.11:84778503::TT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826634, ss5269258943, ss5717011277	NC_000006.12:84068784::TT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826635, ss5269258945	NC_000006.12:84068784::TTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826636	NC_000006.12:84068784::TTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9046718015	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826637	NC_000006.12:84068784::TTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826638	NC_000006.12:84068784::TTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826639	NC_000006.12:84068784::TTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826640	NC_000006.12:84068784::TTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4145826641	NC_000006.12:84068784::TTTTTTTTT	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3503632775	NC_000006.12:84068784:TTTTTTTTTT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT
ss3503632778	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTT:	NC_000006.12:84068784:TTTTTTTTTTTT… NC_000006.12:84068784:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT

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

No publications for rs34220070

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

rs34220070