Name: rs1160758851
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.

rs1160758851

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:97670953-97670976 (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)₁₃ / del(T)₁₂ / del(T)₁₁ / d…
del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₉ / del(T)₈ / del(T)₇ / 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)₁₃ / dup(T)₂₁ / dup(T)₂₂
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.02298 (279/12140, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MTDH : 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	12140	TTTTTTTTTTTTTTTTTTTTTTTT=0.92669	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00008, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00947, TTTTTTTTTTTTTTTTTTTTTTT=0.02298, TTTTTTTTTTTTTTTTTTTTTTTTT=0.02059, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00354, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00692, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00972	0.959906	0.000542	0.039552	0
European	Sub	10250	TTTTTTTTTTTTTTTTTTTTTTTT=0.91327	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00010, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.01122, TTTTTTTTTTTTTTTTTTTTTTT=0.02722, TTTTTTTTTTTTTTTTTTTTTTTTT=0.02439, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00420, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00820, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.01141	0.951666	0.000653	0.047681	0
African	Sub	1366	TTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	56	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1310	TTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	52	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	188	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	30	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	236	TTTTTTTTTTTTTTTTTTTTTTTT=0.996	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.004	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
Allele Frequency Aggregator	Total	Global	12140	(T)₂₄=0.92669	del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00008, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00947, delT=0.02298, dupT=0.02059, dupTT=0.00692, dupTTT=0.00972, dup(T)₆=0.00354
Allele Frequency Aggregator	European	Sub	10250	(T)₂₄=0.91327	del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00010, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.01122, delT=0.02722, dupT=0.02439, dupTT=0.00820, dupTTT=0.01141, dup(T)₆=0.00420
Allele Frequency Aggregator	African	Sub	1366	(T)₂₄=1.0000	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	Other	Sub	236	(T)₂₄=0.996	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=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=0.004, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	188	(T)₂₄=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=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)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	52	(T)₂₄=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=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)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(T)₂₄=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=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)₆=0.00
Allele Frequency Aggregator	Asian	Sub	18	(T)₂₄=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=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)₆=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 8	NC_000008.11:g.97670964_97670976del
GRCh38.p14 chr 8	NC_000008.11:g.97670965_97670976del
GRCh38.p14 chr 8	NC_000008.11:g.97670966_97670976del
GRCh38.p14 chr 8	NC_000008.11:g.97670968_97670976del
GRCh38.p14 chr 8	NC_000008.11:g.97670969_97670976del
GRCh38.p14 chr 8	NC_000008.11:g.97670970_97670976del
GRCh38.p14 chr 8	NC_000008.11:g.97670972_97670976del
GRCh38.p14 chr 8	NC_000008.11:g.97670973_97670976del
GRCh38.p14 chr 8	NC_000008.11:g.97670974_97670976del
GRCh38.p14 chr 8	NC_000008.11:g.97670975_97670976del
GRCh38.p14 chr 8	NC_000008.11:g.97670976del
GRCh38.p14 chr 8	NC_000008.11:g.97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670975_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670974_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670973_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670972_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670971_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670970_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670969_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670968_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670967_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670966_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670965_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670964_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670956_97670976dup
GRCh38.p14 chr 8	NC_000008.11:g.97670955_97670976dup
GRCh37.p13 chr 8	NC_000008.10:g.98683192_98683204del
GRCh37.p13 chr 8	NC_000008.10:g.98683193_98683204del
GRCh37.p13 chr 8	NC_000008.10:g.98683194_98683204del
GRCh37.p13 chr 8	NC_000008.10:g.98683196_98683204del
GRCh37.p13 chr 8	NC_000008.10:g.98683197_98683204del
GRCh37.p13 chr 8	NC_000008.10:g.98683198_98683204del
GRCh37.p13 chr 8	NC_000008.10:g.98683200_98683204del
GRCh37.p13 chr 8	NC_000008.10:g.98683201_98683204del
GRCh37.p13 chr 8	NC_000008.10:g.98683202_98683204del
GRCh37.p13 chr 8	NC_000008.10:g.98683203_98683204del
GRCh37.p13 chr 8	NC_000008.10:g.98683204del
GRCh37.p13 chr 8	NC_000008.10:g.98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683203_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683202_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683201_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683200_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683199_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683198_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683197_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683196_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683195_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683194_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683193_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683192_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683184_98683204dup
GRCh37.p13 chr 8	NC_000008.10:g.98683183_98683204dup

Gene: MTDH, metadherin (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MTDH transcript variant 2	NM_001363136.1:c.483+9791… NM_001363136.1:c.483+9791_483+9803del	N/A	Intron Variant
MTDH transcript variant 3	NM_001363137.1:c.483+9791… NM_001363137.1:c.483+9791_483+9803del	N/A	Intron Variant
MTDH transcript variant 4	NM_001363138.1:c.483+9791… NM_001363138.1:c.483+9791_483+9803del	N/A	Intron Variant
MTDH transcript variant 5	NM_001363139.1:c.483+9791… NM_001363139.1:c.483+9791_483+9803del	N/A	Intron Variant
MTDH transcript variant 1	NM_178812.4:c.483+9791_48… NM_178812.4:c.483+9791_483+9803del	N/A	Intron Variant
MTDH transcript variant X1	XM_011517368.3:c.483+9791… XM_011517368.3:c.483+9791_483+9803del	N/A	Intron Variant
MTDH transcript variant X2	XM_011517369.4:c.483+9791… XM_011517369.4:c.483+9791_483+9803del	N/A	Intron Variant
MTDH transcript variant X3	XM_011517370.4:c.483+9791… XM_011517370.4:c.483+9791_483+9803del	N/A	Intron Variant
MTDH transcript variant X5	XM_017013968.3:c.483+9791… XM_017013968.3:c.483+9791_483+9803del	N/A	Intron Variant
MTDH transcript variant X4	XM_047422418.1:c.483+9791… XM_047422418.1:c.483+9791_483+9803del	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)₁₃	del(T)₁₂	del(T)₁₁	del(T)₉	del(T)₈	del(T)₇	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)₁₃	dup(T)₂₁	dup(T)₂₂
GRCh38.p14 chr 8	NC_000008.11:g.97670953_97670976=	NC_000008.11:g.97670964_97670976del	NC_000008.11:g.97670965_97670976del	NC_000008.11:g.97670966_97670976del	NC_000008.11:g.97670968_97670976del	NC_000008.11:g.97670969_97670976del	NC_000008.11:g.97670970_97670976del	NC_000008.11:g.97670972_97670976del	NC_000008.11:g.97670973_97670976del	NC_000008.11:g.97670974_97670976del	NC_000008.11:g.97670975_97670976del	NC_000008.11:g.97670976del	NC_000008.11:g.97670976dup	NC_000008.11:g.97670975_97670976dup	NC_000008.11:g.97670974_97670976dup	NC_000008.11:g.97670973_97670976dup	NC_000008.11:g.97670972_97670976dup	NC_000008.11:g.97670971_97670976dup	NC_000008.11:g.97670970_97670976dup	NC_000008.11:g.97670969_97670976dup	NC_000008.11:g.97670968_97670976dup	NC_000008.11:g.97670967_97670976dup	NC_000008.11:g.97670966_97670976dup	NC_000008.11:g.97670965_97670976dup	NC_000008.11:g.97670964_97670976dup	NC_000008.11:g.97670956_97670976dup	NC_000008.11:g.97670955_97670976dup
GRCh37.p13 chr 8	NC_000008.10:g.98683181_98683204=	NC_000008.10:g.98683192_98683204del	NC_000008.10:g.98683193_98683204del	NC_000008.10:g.98683194_98683204del	NC_000008.10:g.98683196_98683204del	NC_000008.10:g.98683197_98683204del	NC_000008.10:g.98683198_98683204del	NC_000008.10:g.98683200_98683204del	NC_000008.10:g.98683201_98683204del	NC_000008.10:g.98683202_98683204del	NC_000008.10:g.98683203_98683204del	NC_000008.10:g.98683204del	NC_000008.10:g.98683204dup	NC_000008.10:g.98683203_98683204dup	NC_000008.10:g.98683202_98683204dup	NC_000008.10:g.98683201_98683204dup	NC_000008.10:g.98683200_98683204dup	NC_000008.10:g.98683199_98683204dup	NC_000008.10:g.98683198_98683204dup	NC_000008.10:g.98683197_98683204dup	NC_000008.10:g.98683196_98683204dup	NC_000008.10:g.98683195_98683204dup	NC_000008.10:g.98683194_98683204dup	NC_000008.10:g.98683193_98683204dup	NC_000008.10:g.98683192_98683204dup	NC_000008.10:g.98683184_98683204dup	NC_000008.10:g.98683183_98683204dup
MTDH transcript variant 2	NM_001363136.1:c.483+9780=	NM_001363136.1:c.483+9791_483+9803del	NM_001363136.1:c.483+9792_483+9803del	NM_001363136.1:c.483+9793_483+9803del	NM_001363136.1:c.483+9795_483+9803del	NM_001363136.1:c.483+9796_483+9803del	NM_001363136.1:c.483+9797_483+9803del	NM_001363136.1:c.483+9799_483+9803del	NM_001363136.1:c.483+9800_483+9803del	NM_001363136.1:c.483+9801_483+9803del	NM_001363136.1:c.483+9802_483+9803del	NM_001363136.1:c.483+9803del	NM_001363136.1:c.483+9803dup	NM_001363136.1:c.483+9802_483+9803dup	NM_001363136.1:c.483+9801_483+9803dup	NM_001363136.1:c.483+9800_483+9803dup	NM_001363136.1:c.483+9799_483+9803dup	NM_001363136.1:c.483+9798_483+9803dup	NM_001363136.1:c.483+9797_483+9803dup	NM_001363136.1:c.483+9796_483+9803dup	NM_001363136.1:c.483+9795_483+9803dup	NM_001363136.1:c.483+9794_483+9803dup	NM_001363136.1:c.483+9793_483+9803dup	NM_001363136.1:c.483+9792_483+9803dup	NM_001363136.1:c.483+9791_483+9803dup	NM_001363136.1:c.483+9783_483+9803dup	NM_001363136.1:c.483+9782_483+9803dup
MTDH transcript variant 3	NM_001363137.1:c.483+9780=	NM_001363137.1:c.483+9791_483+9803del	NM_001363137.1:c.483+9792_483+9803del	NM_001363137.1:c.483+9793_483+9803del	NM_001363137.1:c.483+9795_483+9803del	NM_001363137.1:c.483+9796_483+9803del	NM_001363137.1:c.483+9797_483+9803del	NM_001363137.1:c.483+9799_483+9803del	NM_001363137.1:c.483+9800_483+9803del	NM_001363137.1:c.483+9801_483+9803del	NM_001363137.1:c.483+9802_483+9803del	NM_001363137.1:c.483+9803del	NM_001363137.1:c.483+9803dup	NM_001363137.1:c.483+9802_483+9803dup	NM_001363137.1:c.483+9801_483+9803dup	NM_001363137.1:c.483+9800_483+9803dup	NM_001363137.1:c.483+9799_483+9803dup	NM_001363137.1:c.483+9798_483+9803dup	NM_001363137.1:c.483+9797_483+9803dup	NM_001363137.1:c.483+9796_483+9803dup	NM_001363137.1:c.483+9795_483+9803dup	NM_001363137.1:c.483+9794_483+9803dup	NM_001363137.1:c.483+9793_483+9803dup	NM_001363137.1:c.483+9792_483+9803dup	NM_001363137.1:c.483+9791_483+9803dup	NM_001363137.1:c.483+9783_483+9803dup	NM_001363137.1:c.483+9782_483+9803dup
MTDH transcript variant 4	NM_001363138.1:c.483+9780=	NM_001363138.1:c.483+9791_483+9803del	NM_001363138.1:c.483+9792_483+9803del	NM_001363138.1:c.483+9793_483+9803del	NM_001363138.1:c.483+9795_483+9803del	NM_001363138.1:c.483+9796_483+9803del	NM_001363138.1:c.483+9797_483+9803del	NM_001363138.1:c.483+9799_483+9803del	NM_001363138.1:c.483+9800_483+9803del	NM_001363138.1:c.483+9801_483+9803del	NM_001363138.1:c.483+9802_483+9803del	NM_001363138.1:c.483+9803del	NM_001363138.1:c.483+9803dup	NM_001363138.1:c.483+9802_483+9803dup	NM_001363138.1:c.483+9801_483+9803dup	NM_001363138.1:c.483+9800_483+9803dup	NM_001363138.1:c.483+9799_483+9803dup	NM_001363138.1:c.483+9798_483+9803dup	NM_001363138.1:c.483+9797_483+9803dup	NM_001363138.1:c.483+9796_483+9803dup	NM_001363138.1:c.483+9795_483+9803dup	NM_001363138.1:c.483+9794_483+9803dup	NM_001363138.1:c.483+9793_483+9803dup	NM_001363138.1:c.483+9792_483+9803dup	NM_001363138.1:c.483+9791_483+9803dup	NM_001363138.1:c.483+9783_483+9803dup	NM_001363138.1:c.483+9782_483+9803dup
MTDH transcript variant 5	NM_001363139.1:c.483+9780=	NM_001363139.1:c.483+9791_483+9803del	NM_001363139.1:c.483+9792_483+9803del	NM_001363139.1:c.483+9793_483+9803del	NM_001363139.1:c.483+9795_483+9803del	NM_001363139.1:c.483+9796_483+9803del	NM_001363139.1:c.483+9797_483+9803del	NM_001363139.1:c.483+9799_483+9803del	NM_001363139.1:c.483+9800_483+9803del	NM_001363139.1:c.483+9801_483+9803del	NM_001363139.1:c.483+9802_483+9803del	NM_001363139.1:c.483+9803del	NM_001363139.1:c.483+9803dup	NM_001363139.1:c.483+9802_483+9803dup	NM_001363139.1:c.483+9801_483+9803dup	NM_001363139.1:c.483+9800_483+9803dup	NM_001363139.1:c.483+9799_483+9803dup	NM_001363139.1:c.483+9798_483+9803dup	NM_001363139.1:c.483+9797_483+9803dup	NM_001363139.1:c.483+9796_483+9803dup	NM_001363139.1:c.483+9795_483+9803dup	NM_001363139.1:c.483+9794_483+9803dup	NM_001363139.1:c.483+9793_483+9803dup	NM_001363139.1:c.483+9792_483+9803dup	NM_001363139.1:c.483+9791_483+9803dup	NM_001363139.1:c.483+9783_483+9803dup	NM_001363139.1:c.483+9782_483+9803dup
MTDH transcript	NM_178812.3:c.483+9780=	NM_178812.3:c.483+9791_483+9803del	NM_178812.3:c.483+9792_483+9803del	NM_178812.3:c.483+9793_483+9803del	NM_178812.3:c.483+9795_483+9803del	NM_178812.3:c.483+9796_483+9803del	NM_178812.3:c.483+9797_483+9803del	NM_178812.3:c.483+9799_483+9803del	NM_178812.3:c.483+9800_483+9803del	NM_178812.3:c.483+9801_483+9803del	NM_178812.3:c.483+9802_483+9803del	NM_178812.3:c.483+9803del	NM_178812.3:c.483+9803dup	NM_178812.3:c.483+9802_483+9803dup	NM_178812.3:c.483+9801_483+9803dup	NM_178812.3:c.483+9800_483+9803dup	NM_178812.3:c.483+9799_483+9803dup	NM_178812.3:c.483+9798_483+9803dup	NM_178812.3:c.483+9797_483+9803dup	NM_178812.3:c.483+9796_483+9803dup	NM_178812.3:c.483+9795_483+9803dup	NM_178812.3:c.483+9794_483+9803dup	NM_178812.3:c.483+9793_483+9803dup	NM_178812.3:c.483+9792_483+9803dup	NM_178812.3:c.483+9791_483+9803dup	NM_178812.3:c.483+9783_483+9803dup	NM_178812.3:c.483+9782_483+9803dup
MTDH transcript variant 1	NM_178812.4:c.483+9780=	NM_178812.4:c.483+9791_483+9803del	NM_178812.4:c.483+9792_483+9803del	NM_178812.4:c.483+9793_483+9803del	NM_178812.4:c.483+9795_483+9803del	NM_178812.4:c.483+9796_483+9803del	NM_178812.4:c.483+9797_483+9803del	NM_178812.4:c.483+9799_483+9803del	NM_178812.4:c.483+9800_483+9803del	NM_178812.4:c.483+9801_483+9803del	NM_178812.4:c.483+9802_483+9803del	NM_178812.4:c.483+9803del	NM_178812.4:c.483+9803dup	NM_178812.4:c.483+9802_483+9803dup	NM_178812.4:c.483+9801_483+9803dup	NM_178812.4:c.483+9800_483+9803dup	NM_178812.4:c.483+9799_483+9803dup	NM_178812.4:c.483+9798_483+9803dup	NM_178812.4:c.483+9797_483+9803dup	NM_178812.4:c.483+9796_483+9803dup	NM_178812.4:c.483+9795_483+9803dup	NM_178812.4:c.483+9794_483+9803dup	NM_178812.4:c.483+9793_483+9803dup	NM_178812.4:c.483+9792_483+9803dup	NM_178812.4:c.483+9791_483+9803dup	NM_178812.4:c.483+9783_483+9803dup	NM_178812.4:c.483+9782_483+9803dup
MTDH transcript variant X1	XM_005251098.1:c.483+9780=	XM_005251098.1:c.483+9791_483+9803del	XM_005251098.1:c.483+9792_483+9803del	XM_005251098.1:c.483+9793_483+9803del	XM_005251098.1:c.483+9795_483+9803del	XM_005251098.1:c.483+9796_483+9803del	XM_005251098.1:c.483+9797_483+9803del	XM_005251098.1:c.483+9799_483+9803del	XM_005251098.1:c.483+9800_483+9803del	XM_005251098.1:c.483+9801_483+9803del	XM_005251098.1:c.483+9802_483+9803del	XM_005251098.1:c.483+9803del	XM_005251098.1:c.483+9803dup	XM_005251098.1:c.483+9802_483+9803dup	XM_005251098.1:c.483+9801_483+9803dup	XM_005251098.1:c.483+9800_483+9803dup	XM_005251098.1:c.483+9799_483+9803dup	XM_005251098.1:c.483+9798_483+9803dup	XM_005251098.1:c.483+9797_483+9803dup	XM_005251098.1:c.483+9796_483+9803dup	XM_005251098.1:c.483+9795_483+9803dup	XM_005251098.1:c.483+9794_483+9803dup	XM_005251098.1:c.483+9793_483+9803dup	XM_005251098.1:c.483+9792_483+9803dup	XM_005251098.1:c.483+9791_483+9803dup	XM_005251098.1:c.483+9783_483+9803dup	XM_005251098.1:c.483+9782_483+9803dup
MTDH transcript variant X2	XM_005251099.1:c.483+9780=	XM_005251099.1:c.483+9791_483+9803del	XM_005251099.1:c.483+9792_483+9803del	XM_005251099.1:c.483+9793_483+9803del	XM_005251099.1:c.483+9795_483+9803del	XM_005251099.1:c.483+9796_483+9803del	XM_005251099.1:c.483+9797_483+9803del	XM_005251099.1:c.483+9799_483+9803del	XM_005251099.1:c.483+9800_483+9803del	XM_005251099.1:c.483+9801_483+9803del	XM_005251099.1:c.483+9802_483+9803del	XM_005251099.1:c.483+9803del	XM_005251099.1:c.483+9803dup	XM_005251099.1:c.483+9802_483+9803dup	XM_005251099.1:c.483+9801_483+9803dup	XM_005251099.1:c.483+9800_483+9803dup	XM_005251099.1:c.483+9799_483+9803dup	XM_005251099.1:c.483+9798_483+9803dup	XM_005251099.1:c.483+9797_483+9803dup	XM_005251099.1:c.483+9796_483+9803dup	XM_005251099.1:c.483+9795_483+9803dup	XM_005251099.1:c.483+9794_483+9803dup	XM_005251099.1:c.483+9793_483+9803dup	XM_005251099.1:c.483+9792_483+9803dup	XM_005251099.1:c.483+9791_483+9803dup	XM_005251099.1:c.483+9783_483+9803dup	XM_005251099.1:c.483+9782_483+9803dup
MTDH transcript variant X3	XM_005251100.1:c.483+9780=	XM_005251100.1:c.483+9791_483+9803del	XM_005251100.1:c.483+9792_483+9803del	XM_005251100.1:c.483+9793_483+9803del	XM_005251100.1:c.483+9795_483+9803del	XM_005251100.1:c.483+9796_483+9803del	XM_005251100.1:c.483+9797_483+9803del	XM_005251100.1:c.483+9799_483+9803del	XM_005251100.1:c.483+9800_483+9803del	XM_005251100.1:c.483+9801_483+9803del	XM_005251100.1:c.483+9802_483+9803del	XM_005251100.1:c.483+9803del	XM_005251100.1:c.483+9803dup	XM_005251100.1:c.483+9802_483+9803dup	XM_005251100.1:c.483+9801_483+9803dup	XM_005251100.1:c.483+9800_483+9803dup	XM_005251100.1:c.483+9799_483+9803dup	XM_005251100.1:c.483+9798_483+9803dup	XM_005251100.1:c.483+9797_483+9803dup	XM_005251100.1:c.483+9796_483+9803dup	XM_005251100.1:c.483+9795_483+9803dup	XM_005251100.1:c.483+9794_483+9803dup	XM_005251100.1:c.483+9793_483+9803dup	XM_005251100.1:c.483+9792_483+9803dup	XM_005251100.1:c.483+9791_483+9803dup	XM_005251100.1:c.483+9783_483+9803dup	XM_005251100.1:c.483+9782_483+9803dup
MTDH transcript variant X1	XM_011517368.3:c.483+9780=	XM_011517368.3:c.483+9791_483+9803del	XM_011517368.3:c.483+9792_483+9803del	XM_011517368.3:c.483+9793_483+9803del	XM_011517368.3:c.483+9795_483+9803del	XM_011517368.3:c.483+9796_483+9803del	XM_011517368.3:c.483+9797_483+9803del	XM_011517368.3:c.483+9799_483+9803del	XM_011517368.3:c.483+9800_483+9803del	XM_011517368.3:c.483+9801_483+9803del	XM_011517368.3:c.483+9802_483+9803del	XM_011517368.3:c.483+9803del	XM_011517368.3:c.483+9803dup	XM_011517368.3:c.483+9802_483+9803dup	XM_011517368.3:c.483+9801_483+9803dup	XM_011517368.3:c.483+9800_483+9803dup	XM_011517368.3:c.483+9799_483+9803dup	XM_011517368.3:c.483+9798_483+9803dup	XM_011517368.3:c.483+9797_483+9803dup	XM_011517368.3:c.483+9796_483+9803dup	XM_011517368.3:c.483+9795_483+9803dup	XM_011517368.3:c.483+9794_483+9803dup	XM_011517368.3:c.483+9793_483+9803dup	XM_011517368.3:c.483+9792_483+9803dup	XM_011517368.3:c.483+9791_483+9803dup	XM_011517368.3:c.483+9783_483+9803dup	XM_011517368.3:c.483+9782_483+9803dup
MTDH transcript variant X2	XM_011517369.4:c.483+9780=	XM_011517369.4:c.483+9791_483+9803del	XM_011517369.4:c.483+9792_483+9803del	XM_011517369.4:c.483+9793_483+9803del	XM_011517369.4:c.483+9795_483+9803del	XM_011517369.4:c.483+9796_483+9803del	XM_011517369.4:c.483+9797_483+9803del	XM_011517369.4:c.483+9799_483+9803del	XM_011517369.4:c.483+9800_483+9803del	XM_011517369.4:c.483+9801_483+9803del	XM_011517369.4:c.483+9802_483+9803del	XM_011517369.4:c.483+9803del	XM_011517369.4:c.483+9803dup	XM_011517369.4:c.483+9802_483+9803dup	XM_011517369.4:c.483+9801_483+9803dup	XM_011517369.4:c.483+9800_483+9803dup	XM_011517369.4:c.483+9799_483+9803dup	XM_011517369.4:c.483+9798_483+9803dup	XM_011517369.4:c.483+9797_483+9803dup	XM_011517369.4:c.483+9796_483+9803dup	XM_011517369.4:c.483+9795_483+9803dup	XM_011517369.4:c.483+9794_483+9803dup	XM_011517369.4:c.483+9793_483+9803dup	XM_011517369.4:c.483+9792_483+9803dup	XM_011517369.4:c.483+9791_483+9803dup	XM_011517369.4:c.483+9783_483+9803dup	XM_011517369.4:c.483+9782_483+9803dup
MTDH transcript variant X3	XM_011517370.4:c.483+9780=	XM_011517370.4:c.483+9791_483+9803del	XM_011517370.4:c.483+9792_483+9803del	XM_011517370.4:c.483+9793_483+9803del	XM_011517370.4:c.483+9795_483+9803del	XM_011517370.4:c.483+9796_483+9803del	XM_011517370.4:c.483+9797_483+9803del	XM_011517370.4:c.483+9799_483+9803del	XM_011517370.4:c.483+9800_483+9803del	XM_011517370.4:c.483+9801_483+9803del	XM_011517370.4:c.483+9802_483+9803del	XM_011517370.4:c.483+9803del	XM_011517370.4:c.483+9803dup	XM_011517370.4:c.483+9802_483+9803dup	XM_011517370.4:c.483+9801_483+9803dup	XM_011517370.4:c.483+9800_483+9803dup	XM_011517370.4:c.483+9799_483+9803dup	XM_011517370.4:c.483+9798_483+9803dup	XM_011517370.4:c.483+9797_483+9803dup	XM_011517370.4:c.483+9796_483+9803dup	XM_011517370.4:c.483+9795_483+9803dup	XM_011517370.4:c.483+9794_483+9803dup	XM_011517370.4:c.483+9793_483+9803dup	XM_011517370.4:c.483+9792_483+9803dup	XM_011517370.4:c.483+9791_483+9803dup	XM_011517370.4:c.483+9783_483+9803dup	XM_011517370.4:c.483+9782_483+9803dup
MTDH transcript variant X5	XM_017013968.3:c.483+9780=	XM_017013968.3:c.483+9791_483+9803del	XM_017013968.3:c.483+9792_483+9803del	XM_017013968.3:c.483+9793_483+9803del	XM_017013968.3:c.483+9795_483+9803del	XM_017013968.3:c.483+9796_483+9803del	XM_017013968.3:c.483+9797_483+9803del	XM_017013968.3:c.483+9799_483+9803del	XM_017013968.3:c.483+9800_483+9803del	XM_017013968.3:c.483+9801_483+9803del	XM_017013968.3:c.483+9802_483+9803del	XM_017013968.3:c.483+9803del	XM_017013968.3:c.483+9803dup	XM_017013968.3:c.483+9802_483+9803dup	XM_017013968.3:c.483+9801_483+9803dup	XM_017013968.3:c.483+9800_483+9803dup	XM_017013968.3:c.483+9799_483+9803dup	XM_017013968.3:c.483+9798_483+9803dup	XM_017013968.3:c.483+9797_483+9803dup	XM_017013968.3:c.483+9796_483+9803dup	XM_017013968.3:c.483+9795_483+9803dup	XM_017013968.3:c.483+9794_483+9803dup	XM_017013968.3:c.483+9793_483+9803dup	XM_017013968.3:c.483+9792_483+9803dup	XM_017013968.3:c.483+9791_483+9803dup	XM_017013968.3:c.483+9783_483+9803dup	XM_017013968.3:c.483+9782_483+9803dup
MTDH transcript variant X4	XM_047422418.1:c.483+9780=	XM_047422418.1:c.483+9791_483+9803del	XM_047422418.1:c.483+9792_483+9803del	XM_047422418.1:c.483+9793_483+9803del	XM_047422418.1:c.483+9795_483+9803del	XM_047422418.1:c.483+9796_483+9803del	XM_047422418.1:c.483+9797_483+9803del	XM_047422418.1:c.483+9799_483+9803del	XM_047422418.1:c.483+9800_483+9803del	XM_047422418.1:c.483+9801_483+9803del	XM_047422418.1:c.483+9802_483+9803del	XM_047422418.1:c.483+9803del	XM_047422418.1:c.483+9803dup	XM_047422418.1:c.483+9802_483+9803dup	XM_047422418.1:c.483+9801_483+9803dup	XM_047422418.1:c.483+9800_483+9803dup	XM_047422418.1:c.483+9799_483+9803dup	XM_047422418.1:c.483+9798_483+9803dup	XM_047422418.1:c.483+9797_483+9803dup	XM_047422418.1:c.483+9796_483+9803dup	XM_047422418.1:c.483+9795_483+9803dup	XM_047422418.1:c.483+9794_483+9803dup	XM_047422418.1:c.483+9793_483+9803dup	XM_047422418.1:c.483+9792_483+9803dup	XM_047422418.1:c.483+9791_483+9803dup	XM_047422418.1:c.483+9783_483+9803dup	XM_047422418.1:c.483+9782_483+9803dup

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#.

34 SubSNP, 31 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3003673382	Jan 10, 2018 (151)
2	GNOMAD	ss4189836664	Apr 26, 2021 (155)
3	GNOMAD	ss4189836665	Apr 26, 2021 (155)
4	GNOMAD	ss4189836669	Apr 26, 2021 (155)
5	GNOMAD	ss4189836670	Apr 26, 2021 (155)
6	GNOMAD	ss4189836671	Apr 26, 2021 (155)
7	GNOMAD	ss4189836672	Apr 26, 2021 (155)
8	GNOMAD	ss4189836673	Apr 26, 2021 (155)
9	GNOMAD	ss4189836674	Apr 26, 2021 (155)
10	GNOMAD	ss4189836675	Apr 26, 2021 (155)
11	GNOMAD	ss4189836676	Apr 26, 2021 (155)
12	GNOMAD	ss4189836677	Apr 26, 2021 (155)
13	GNOMAD	ss4189836678	Apr 26, 2021 (155)
14	GNOMAD	ss4189836679	Apr 26, 2021 (155)
15	GNOMAD	ss4189836681	Apr 26, 2021 (155)
16	GNOMAD	ss4189836682	Apr 26, 2021 (155)
17	GNOMAD	ss4189836683	Apr 26, 2021 (155)
18	GNOMAD	ss4189836684	Apr 26, 2021 (155)
19	GNOMAD	ss4189836685	Apr 26, 2021 (155)
20	GNOMAD	ss4189836686	Apr 26, 2021 (155)
21	GNOMAD	ss4189836687	Apr 26, 2021 (155)
22	GNOMAD	ss4189836688	Apr 26, 2021 (155)
23	GNOMAD	ss4189836689	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5190080330	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5190080331	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5190080332	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5190080333	Apr 26, 2021 (155)
28	HUGCELL_USP	ss5474675818	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5474675819	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5474675820	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5732543476	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5732543477	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5732543478	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5732543480	Oct 16, 2022 (156)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 305134361 (NC_000008.11:97670952::T 7390/73780) Row 305134362 (NC_000008.11:97670952::TT 2198/73706) Row 305134366 (NC_000008.11:97670952::TTTT 568/73766)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 48049637 (NC_000008.10:98683180:T: 2396/15478) Row 48049638 (NC_000008.10:98683180:TT: 1475/15478) Row 48049639 (NC_000008.10:98683180::T 159/15478)...	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 48049637 (NC_000008.10:98683180:T: 2396/15478) Row 48049638 (NC_000008.10:98683180:TT: 1475/15478) Row 48049639 (NC_000008.10:98683180::T 159/15478)...	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 48049637 (NC_000008.10:98683180:T: 2396/15478) Row 48049638 (NC_000008.10:98683180:TT: 1475/15478) Row 48049639 (NC_000008.10:98683180::T 159/15478)...	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 48049637 (NC_000008.10:98683180:T: 2396/15478) Row 48049638 (NC_000008.10:98683180:TT: 1475/15478) Row 48049639 (NC_000008.10:98683180::T 159/15478)...	-	Apr 26, 2021 (155)
61	14KJPN Submission ignored due to conflicting rows: Row 66380580 (NC_000008.11:97670952::T 290/24516) Row 66380581 (NC_000008.11:97670952:TT: 2592/24516) Row 66380582 (NC_000008.11:97670952:T: 4165/24516)...	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 66380580 (NC_000008.11:97670952::T 290/24516) Row 66380581 (NC_000008.11:97670952:TT: 2592/24516) Row 66380582 (NC_000008.11:97670952:T: 4165/24516)...	-	Oct 16, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 66380580 (NC_000008.11:97670952::T 290/24516) Row 66380581 (NC_000008.11:97670952:TT: 2592/24516) Row 66380582 (NC_000008.11:97670952:T: 4165/24516)...	-	Oct 16, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 66380580 (NC_000008.11:97670952::T 290/24516) Row 66380581 (NC_000008.11:97670952:TT: 2592/24516) Row 66380582 (NC_000008.11:97670952:T: 4165/24516)...	-	Oct 16, 2022 (156)
65	ALFA	NC_000008.11 - 97670953	Apr 26, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4189836689	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTT:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4189836688	NC_000008.11:97670952:TTTTTTTTTTTT:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4189836687	NC_000008.11:97670952:TTTTTTTTTTT:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4189836686	NC_000008.11:97670952:TTTTTTTTT:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4189836685	NC_000008.11:97670952:TTTTTTT:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4189836684	NC_000008.11:97670952:TTTTT:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4189836683	NC_000008.11:97670952:TTT:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3003673382, ss5190080331	NC_000008.10:98683180:TT:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836682, ss5474675820, ss5732543477	NC_000008.11:97670952:TT:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5190080330	NC_000008.10:98683180:T:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836681, ss5474675819, ss5732543478	NC_000008.11:97670952:T:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5190080332	NC_000008.10:98683180::T	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836664, ss5474675818, ss5732543476	NC_000008.11:97670952::T	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5190080333	NC_000008.10:98683180::TT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836665, ss5732543480	NC_000008.11:97670952::TT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836669	NC_000008.11:97670952::TTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836670	NC_000008.11:97670952::TTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4307157292	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836671	NC_000008.11:97670952::TTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836672	NC_000008.11:97670952::TTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836673	NC_000008.11:97670952::TTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836674	NC_000008.11:97670952::TTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836675	NC_000008.11:97670952::TTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836676	NC_000008.11:97670952::TTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836677	NC_000008.11:97670952::TTTTTTTTTTT… NC_000008.11:97670952::TTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836678	NC_000008.11:97670952::TTTTTTTTTTT… NC_000008.11:97670952::TTTTTTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4189836679	NC_000008.11:97670952::TTTTTTTTTTT… NC_000008.11:97670952::TTTTTTTTTTTTTTTTTTTTTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3570375074	NC_000008.11:97670952::TTT	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
ss3570375079	NC_000008.11:97670952:TTTT:	NC_000008.11:97670952:TTTTTTTTTTTT… NC_000008.11:97670952:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

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

No publications for rs1160758851

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

rs1160758851