Name: rs1491410388
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.

rs1491410388

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:7887794-7887800 (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: ins(CATA)₂TATATA / ins(CATA)₂TATAT…
ins(CATA)₂TATATA / ins(CATA)₂TATATATA / ins(CATA)₂TATATATATA / ins(CATATA)₂TATATATA / ins(CATATATA)₂TA / ins(CATATATA)₂TATATA / insC(AT)₄A / insC(AT)₅A / insC(AT)₆A / insC(AT)₆AC(AT)₄A / insC(AT)₇A / insC(AT)₈A / insC(AT)₉A / insC(AT)₁₀A / insC(AT)₁₁A / insC(AT)₁₂A / insC(AT)₁₃A / insC(AT)₁₄A / insC(AT)₁₅A / insC(AT)₁₆A / insC(AT)₁₇A
Variation Type: Indel Insertion and Deletion
Frequency: insC(AT)₈A=0.05619 (1586/28224, 14KJPN)
ins(CATA)₂TATATATATA=0.00000 (0/11750, ALFA)
insC(AT)₄A=0.00000 (0/11750, ALFA) (+ 4 more)
insC(AT)₅A=0.00000 (0/11750, ALFA)
insC(AT)₆A=0.00000 (0/11750, ALFA)
insC(AT)₇A=0.00000 (0/11750, ALFA)
insC(AT)₈A=0.00000 (0/11750, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MTRR : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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
14KJPN	JAPANESE	Study-wide	28224	- No frequency provided	insC(AT)₈A=0.05619
Allele Frequency Aggregator	Total	Global	11750	(AT)₃A=1.00000	ins(CATA)₂TATATATATA=0.00000, insC(AT)₄A=0.00000, insC(AT)₅A=0.00000, insC(AT)₆A=0.00000, insC(AT)₇A=0.00000, insC(AT)₈A=0.00000
Allele Frequency Aggregator	European	Sub	7568	(AT)₃A=1.0000	ins(CATA)₂TATATATATA=0.0000, insC(AT)₄A=0.0000, insC(AT)₅A=0.0000, insC(AT)₆A=0.0000, insC(AT)₇A=0.0000, insC(AT)₈A=0.0000
Allele Frequency Aggregator	African	Sub	2772	(AT)₃A=1.0000	ins(CATA)₂TATATATATA=0.0000, insC(AT)₄A=0.0000, insC(AT)₅A=0.0000, insC(AT)₆A=0.0000, insC(AT)₇A=0.0000, insC(AT)₈A=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	598	(AT)₃A=1.000	ins(CATA)₂TATATATATA=0.000, insC(AT)₄A=0.000, insC(AT)₅A=0.000, insC(AT)₆A=0.000, insC(AT)₇A=0.000, insC(AT)₈A=0.000
Allele Frequency Aggregator	Other	Sub	466	(AT)₃A=1.000	ins(CATA)₂TATATATATA=0.000, insC(AT)₄A=0.000, insC(AT)₅A=0.000, insC(AT)₆A=0.000, insC(AT)₇A=0.000, insC(AT)₈A=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	(AT)₃A=1.000	ins(CATA)₂TATATATATA=0.000, insC(AT)₄A=0.000, insC(AT)₅A=0.000, insC(AT)₆A=0.000, insC(AT)₇A=0.000, insC(AT)₈A=0.000
Allele Frequency Aggregator	Asian	Sub	108	(AT)₃A=1.000	ins(CATA)₂TATATATATA=0.000, insC(AT)₄A=0.000, insC(AT)₅A=0.000, insC(AT)₆A=0.000, insC(AT)₇A=0.000, insC(AT)₈A=0.000
Allele Frequency Aggregator	South Asian	Sub	92	(AT)₃A=1.00	ins(CATA)₂TATATATATA=0.00, insC(AT)₄A=0.00, insC(AT)₅A=0.00, insC(AT)₆A=0.00, insC(AT)₇A=0.00, insC(AT)₈A=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 5	NC_000005.10:g.7887794_7887800AT[3]ACAT[2]AT[3]A[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACAT[2]AT[4]A[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACAT[2]AT[5]A[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATAT[2]AT[4]A[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800ATATATAC[2]AT[4]A[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800ATATATAC[2]AT[6]A[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800ATATATACATATAT[2]ATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATATATATATA[1]
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACAT[2]AT[3]A[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACAT[2]AT[4]A[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACAT[2]AT[5]A[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATAT[2]AT[4]A[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913ATATATAC[2]AT[4]A[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913ATATATAC[2]AT[6]A[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913ATATATACATATAT[2]ATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACAT[2]AT[3]A[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACAT[2]AT[4]A[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACAT[2]AT[5]A[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATAT[2]AT[4]A[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697ATATATAC[2]AT[4]A[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697ATATATAC[2]AT[6]A[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697ATATATACATATAT[2]ATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATATATATATATA[1]

Gene: MTRR, 5-methyltetrahydrofolate-homocysteine methyltransferase reductase (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MTRR transcript variant 6	NM_001364440.2:c.1146+109… NM_001364440.2:c.1146+1097_1146+1098insCATACATATATATA	N/A	Intron Variant
MTRR transcript variant 7	NM_001364441.2:c.1146+109… NM_001364441.2:c.1146+1097_1146+1098insCATACATATATATA	N/A	Intron Variant
MTRR transcript variant 8	NM_001364442.2:c.1146+109… NM_001364442.2:c.1146+1097_1146+1098insCATACATATATATA	N/A	Intron Variant
MTRR transcript variant 1	NM_002454.3:c.1146+1097_1… NM_002454.3:c.1146+1097_1146+1098insCATACATATATATA	N/A	Intron Variant
MTRR transcript variant 2	NM_024010.4:c.1146+1097_1… NM_024010.4:c.1146+1097_1146+1098insCATACATATATATA	N/A	Intron Variant
MTRR transcript variant 3	NR_134480.2:n.	N/A	Intron Variant
MTRR transcript variant 4	NR_134481.2:n.	N/A	Intron Variant
MTRR transcript variant 5	NR_134482.2:n.	N/A	Intron Variant
MTRR transcript variant 9	NR_157168.2:n.	N/A	Intron Variant
MTRR transcript variant 10	NR_157169.2:n.	N/A	Intron Variant
MTRR transcript variant 11	NR_157170.2:n.	N/A	Intron Variant
MTRR transcript variant 12	NR_157171.2:n.	N/A	Intron Variant
MTRR transcript variant 13	NR_157172.2:n.	N/A	Intron Variant
MTRR transcript variant 14	NR_157173.2:n.	N/A	Intron Variant
MTRR transcript variant 15	NR_157174.2:n.	N/A	Intron Variant
MTRR transcript variant 16	NR_157175.2:n.	N/A	Intron Variant
MTRR transcript variant 17	NR_157176.2:n.	N/A	Intron Variant
MTRR transcript variant 18	NR_157177.2:n.	N/A	Intron Variant
MTRR transcript variant 19	NR_157178.2:n.	N/A	Intron Variant
MTRR transcript variant X1	XM_024446064.2:c.1146+109… XM_024446064.2:c.1146+1097_1146+1098insCATACATATATATA	N/A	Intron Variant
MTRR transcript variant X2	XM_047417233.1:c.1146+109… XM_047417233.1:c.1146+1097_1146+1098insCATACATATATATA	N/A	Intron Variant
MTRR transcript variant X3	XM_047417234.1:c.1146+109… XM_047417234.1:c.1146+1097_1146+1098insCATACATATATATA	N/A	Intron Variant
MTRR transcript variant X4	XM_047417235.1:c.1169+107… XM_047417235.1:c.1169+1074_1169+1075insCATACATATATATA	N/A	Intron Variant
MTRR transcript variant X5	XM_047417236.1:c.1146+109… XM_047417236.1:c.1146+1097_1146+1098insCATACATATATATA	N/A	Intron Variant
MTRR transcript variant X6	XM_047417237.1:c.1058-129… XM_047417237.1:c.1058-1295_1058-1294insCATACATATATATA	N/A	Intron Variant
MTRR transcript variant X7	XM_047417238.1:c.	N/A	Genic Downstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(AT)₃A=	ins(CATA)₂TATATA	ins(CATA)₂TATATATA	ins(CATA)₂TATATATATA	ins(CATATA)₂TATATATA	ins(CATATATA)₂TA	ins(CATATATA)₂TATATA	insC(AT)₄A	insC(AT)₅A	insC(AT)₆A	insC(AT)₆AC(AT)₄A	insC(AT)₇A	insC(AT)₈A	insC(AT)₉A	insC(AT)₁₀A	insC(AT)₁₁A	insC(AT)₁₂A	insC(AT)₁₃A	insC(AT)₁₄A	insC(AT)₁₅A	insC(AT)₁₆A	insC(AT)₁₇A
GRCh38.p14 chr 5	NC_000005.10:g.7887794_7887800=	NC_000005.10:g.7887794_7887800AT[3]ACAT[2]AT[3]A[1]	NC_000005.10:g.7887794_7887800AT[3]ACAT[2]AT[4]A[1]	NC_000005.10:g.7887794_7887800AT[3]ACAT[2]AT[5]A[1]	NC_000005.10:g.7887794_7887800AT[3]ACATAT[2]AT[4]A[1]	NC_000005.10:g.7887794_7887800ATATATAC[2]AT[4]A[1]	NC_000005.10:g.7887794_7887800ATATATAC[2]AT[6]A[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATA[1]	NC_000005.10:g.7887794_7887800ATATATACATATAT[2]ATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATATATATATA[1]	NC_000005.10:g.7887794_7887800AT[3]ACATATATATATATATATATATATATATATATATATA[1]
GRCh37.p13 chr 5	NC_000005.9:g.7887907_7887913=	NC_000005.9:g.7887907_7887913AT[3]ACAT[2]AT[3]A[1]	NC_000005.9:g.7887907_7887913AT[3]ACAT[2]AT[4]A[1]	NC_000005.9:g.7887907_7887913AT[3]ACAT[2]AT[5]A[1]	NC_000005.9:g.7887907_7887913AT[3]ACATAT[2]AT[4]A[1]	NC_000005.9:g.7887907_7887913ATATATAC[2]AT[4]A[1]	NC_000005.9:g.7887907_7887913ATATATAC[2]AT[6]A[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATA[1]	NC_000005.9:g.7887907_7887913ATATATACATATAT[2]ATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATATATATATA[1]	NC_000005.9:g.7887907_7887913AT[3]ACATATATATATATATATATATATATATATATATATA[1]
MTRR RefSeqGene	NG_008856.1:g.23691_23697=	NG_008856.1:g.23691_23697AT[3]ACAT[2]AT[3]A[1]	NG_008856.1:g.23691_23697AT[3]ACAT[2]AT[4]A[1]	NG_008856.1:g.23691_23697AT[3]ACAT[2]AT[5]A[1]	NG_008856.1:g.23691_23697AT[3]ACATAT[2]AT[4]A[1]	NG_008856.1:g.23691_23697ATATATAC[2]AT[4]A[1]	NG_008856.1:g.23691_23697ATATATAC[2]AT[6]A[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATA[1]	NG_008856.1:g.23691_23697ATATATACATATAT[2]ATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATATATATATA[1]	NG_008856.1:g.23691_23697AT[3]ACATATATATATATATATATATATATATATATATATA[1]
MTRR transcript variant 6	NM_001364440.2:c.1146+1091=	NM_001364440.2:c.1146+1097_1146+1098insCATACATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATACATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATACATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATACATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATACATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATACATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATACATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATA	NM_001364440.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant 7	NM_001364441.2:c.1146+1091=	NM_001364441.2:c.1146+1097_1146+1098insCATACATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATACATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATACATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATACATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATACATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATACATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATACATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATA	NM_001364441.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant 8	NM_001364442.2:c.1146+1091=	NM_001364442.2:c.1146+1097_1146+1098insCATACATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATACATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATACATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATACATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATACATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATACATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATACATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATA	NM_001364442.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant 1	NM_002454.2:c.1146+1091=	NM_002454.2:c.1146+1097_1146+1098insCATACATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATACATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATACATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATACATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATACATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATACATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATACATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATA	NM_002454.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant 1	NM_002454.3:c.1146+1091=	NM_002454.3:c.1146+1097_1146+1098insCATACATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATACATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATACATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATACATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATACATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATACATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATACATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATATATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATA	NM_002454.3:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant 2	NM_024010.2:c.1227+1091=	NM_024010.2:c.1227+1097_1227+1098insCATACATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATACATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATACATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATACATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATACATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATACATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATACATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATATATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATATATATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATATATATATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATATATATATATATATATATATA	NM_024010.2:c.1227+1097_1227+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant 2	NM_024010.4:c.1146+1091=	NM_024010.4:c.1146+1097_1146+1098insCATACATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATACATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATACATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATACATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATACATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATACATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATACATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATATATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATA	NM_024010.4:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant X1	XM_005248304.1:c.1191+1091=	XM_005248304.1:c.1191+1097_1191+1098insCATACATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATACATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATACATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATACATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATACATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATACATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATACATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATATATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATATATATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATATATATATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATATATATATATATATATATATA	XM_005248304.1:c.1191+1097_1191+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant X2	XM_005248305.1:c.1146+1091=	XM_005248305.1:c.1146+1097_1146+1098insCATACATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATACATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATACATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATACATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATACATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATACATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATACATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATA	XM_005248305.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant X1	XM_024446064.2:c.1146+1091=	XM_024446064.2:c.1146+1097_1146+1098insCATACATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATACATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATACATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATACATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATACATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATACATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATACATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATA	XM_024446064.2:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant X2	XM_047417233.1:c.1146+1091=	XM_047417233.1:c.1146+1097_1146+1098insCATACATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATACATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATACATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATACATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATACATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATACATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATACATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATA	XM_047417233.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant X3	XM_047417234.1:c.1146+1091=	XM_047417234.1:c.1146+1097_1146+1098insCATACATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATACATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATACATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATACATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATACATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATACATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATACATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATA	XM_047417234.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant X4	XM_047417235.1:c.1169+1068=	XM_047417235.1:c.1169+1074_1169+1075insCATACATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATACATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATACATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATACATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATACATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATACATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATACATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATATATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATATATATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATATATATATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATATATATATATATATATATATA	XM_047417235.1:c.1169+1074_1169+1075insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant X5	XM_047417236.1:c.1146+1091=	XM_047417236.1:c.1146+1097_1146+1098insCATACATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATACATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATACATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATACATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATACATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATACATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATACATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATA	XM_047417236.1:c.1146+1097_1146+1098insCATATATATATATATATATATATATATATATATATA
MTRR transcript variant X6	XM_047417237.1:c.1058-1301=	XM_047417237.1:c.1058-1295_1058-1294insCATACATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATACATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATACATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATACATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATACATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATACATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATACATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATATATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATATATATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATATATATATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATATATATATATATATATATATA	XM_047417237.1:c.1058-1295_1058-1294insCATATATATATATATATATATATATATATATATATA

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#.

24 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PACBIO	ss3785016907	Jul 13, 2019 (153)
2	PACBIO	ss3795312350	Jul 13, 2019 (153)
3	GNOMAD	ss4098919215	Apr 26, 2021 (155)
4	GNOMAD	ss4098919216	Apr 26, 2021 (155)
5	GNOMAD	ss4098919217	Apr 26, 2021 (155)
6	GNOMAD	ss4098919218	Apr 26, 2021 (155)
7	GNOMAD	ss4098919219	Apr 26, 2021 (155)
8	GNOMAD	ss4098919220	Apr 26, 2021 (155)
9	GNOMAD	ss4098919221	Apr 26, 2021 (155)
10	GNOMAD	ss4098919222	Apr 26, 2021 (155)
11	GNOMAD	ss4098919223	Apr 26, 2021 (155)
12	GNOMAD	ss4098919224	Apr 26, 2021 (155)
13	GNOMAD	ss4098919225	Apr 26, 2021 (155)
14	GNOMAD	ss4098919226	Apr 26, 2021 (155)
15	GNOMAD	ss4098919227	Apr 26, 2021 (155)
16	GNOMAD	ss4098919228	Apr 26, 2021 (155)
17	GNOMAD	ss4098919229	Apr 26, 2021 (155)
18	GNOMAD	ss4098919230	Apr 26, 2021 (155)
19	GNOMAD	ss4098919231	Apr 26, 2021 (155)
20	GNOMAD	ss4098919232	Apr 26, 2021 (155)
21	GNOMAD	ss4098919233	Apr 26, 2021 (155)
22	GNOMAD	ss4098919234	Apr 26, 2021 (155)
23	GNOMAD	ss4098919235	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5705931774	Oct 13, 2022 (156)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179304916 (NC_000005.10:7887793::ATATATACAT 1178/85074) Row 179304917 (NC_000005.10:7887793::ATATATACATACAT 1/85124) Row 179304918 (NC_000005.10:7887793::ATATATACATACATAT 1/85124)...	-	Apr 26, 2021 (155)
46	14KJPN	NC_000005.10 - 7887794	Oct 13, 2022 (156)
47	ALFA	NC_000005.10 - 7887794	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
ss4098919216	NC_000005.10:7887793::ATATATACATAC… NC_000005.10:7887793::ATATATACATACAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATACATATATATA	(self)
ss4098919217	NC_000005.10:7887793::ATATATACATAC… NC_000005.10:7887793::ATATATACATACATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATACATATATATATA	(self)
ss4098919218	NC_000005.10:7887793::ATATATACATAC… NC_000005.10:7887793::ATATATACATACATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATACATATATATATATA	(self)
4893053135	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATACATATATATATATA	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATACATATATATATATA	(self)
ss4098919220	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATACATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATACATATATATATATA	(self)
ss4098919222	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATACAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATACATATATATA	(self)
ss4098919223	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATACATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATACATATATATATATA	(self)
ss3785016907	NC_000005.9:7887906::ATATATACAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATA	(self)
ss4098919215	NC_000005.10:7887793::ATATATACAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATA	(self)
4893053135	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATA	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATA	(self)
ss4098919219	NC_000005.10:7887793::ATATATACATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATA	(self)
4893053135	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATA	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATA	(self)
ss4098919221	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATA	(self)
4893053135	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATA	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATA	(self)
ss4098919227	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATATATATACAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATACATATATATA	(self)
ss4098919224	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATA	(self)
4893053135	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATA	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATA	(self)
ss3795312350	NC_000005.9:7887906::ATATATACATATA… NC_000005.9:7887906::ATATATACATATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATA	(self)
39768878, ss4098919225, ss5705931774	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATA	(self)
4893053135	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATA	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATA	(self)
ss4098919226	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATATA	(self)
ss4098919228	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATATATA	(self)
ss4098919229	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATATATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATATATATA	(self)
ss4098919230	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATATATATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATATATATATA	(self)
ss4098919231	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATATATATATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATATATATATATA	(self)
ss4098919232	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATATATATATATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATATATATATATATA	(self)
ss4098919233	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATATATATATATATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATATATATATATATATA	(self)
ss4098919234	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATATATATATATATATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATATATATATATATATATA	(self)
ss4098919235	NC_000005.10:7887793::ATATATACATAT… NC_000005.10:7887793::ATATATACATATATATATATATATATATATATATAT	NC_000005.10:7887793:ATATATA:ATATA… NC_000005.10:7887793:ATATATA:ATATATACATATATATATATATATATATATATATATATATATA	(self)

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

No publications for rs1491410388

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
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491410388