Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

dbSNP Short Genetic Variations

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

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 11750 ATATATA=1.00000 ATATATACATACATATATATATATA=0.00000, ATATATACATATATATA=0.00000, ATATATACATATATATATA=0.00000, ATATATACATATATATATATA=0.00000, ATATATACATATATATATATATA=0.00000, ATATATACATATATATATATATATA=0.00000 1.0 0.0 0.0 N/A
European Sub 7568 ATATATA=1.0000 ATATATACATACATATATATATATA=0.0000, ATATATACATATATATA=0.0000, ATATATACATATATATATA=0.0000, ATATATACATATATATATATA=0.0000, ATATATACATATATATATATATA=0.0000, ATATATACATATATATATATATATA=0.0000 1.0 0.0 0.0 N/A
African Sub 2772 ATATATA=1.0000 ATATATACATACATATATATATATA=0.0000, ATATATACATATATATA=0.0000, ATATATACATATATATATA=0.0000, ATATATACATATATATATATA=0.0000, ATATATACATATATATATATATA=0.0000, ATATATACATATATATATATATATA=0.0000 1.0 0.0 0.0 N/A
African Others Sub 106 ATATATA=1.000 ATATATACATACATATATATATATA=0.000, ATATATACATATATATA=0.000, ATATATACATATATATATA=0.000, ATATATACATATATATATATA=0.000, ATATATACATATATATATATATA=0.000, ATATATACATATATATATATATATA=0.000 1.0 0.0 0.0 N/A
African American Sub 2666 ATATATA=1.0000 ATATATACATACATATATATATATA=0.0000, ATATATACATATATATA=0.0000, ATATATACATATATATATA=0.0000, ATATATACATATATATATATA=0.0000, ATATATACATATATATATATATA=0.0000, ATATATACATATATATATATATATA=0.0000 1.0 0.0 0.0 N/A
Asian Sub 108 ATATATA=1.000 ATATATACATACATATATATATATA=0.000, ATATATACATATATATA=0.000, ATATATACATATATATATA=0.000, ATATATACATATATATATATA=0.000, ATATATACATATATATATATATA=0.000, ATATATACATATATATATATATATA=0.000 1.0 0.0 0.0 N/A
East Asian Sub 84 ATATATA=1.00 ATATATACATACATATATATATATA=0.00, ATATATACATATATATA=0.00, ATATATACATATATATATA=0.00, ATATATACATATATATATATA=0.00, ATATATACATATATATATATATA=0.00, ATATATACATATATATATATATATA=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 24 ATATATA=1.00 ATATATACATACATATATATATATA=0.00, ATATATACATATATATA=0.00, ATATATACATATATATATA=0.00, ATATATACATATATATATATA=0.00, ATATATACATATATATATATATA=0.00, ATATATACATATATATATATATATA=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 ATATATA=1.000 ATATATACATACATATATATATATA=0.000, ATATATACATATATATA=0.000, ATATATACATATATATATA=0.000, ATATATACATATATATATATA=0.000, ATATATACATATATATATATATA=0.000, ATATATACATATATATATATATATA=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 598 ATATATA=1.000 ATATATACATACATATATATATATA=0.000, ATATATACATATATATA=0.000, ATATATACATATATATATA=0.000, ATATATACATATATATATATA=0.000, ATATATACATATATATATATATA=0.000, ATATATACATATATATATATATATA=0.000 1.0 0.0 0.0 N/A
South Asian Sub 92 ATATATA=1.00 ATATATACATACATATATATATATA=0.00, ATATATACATATATATA=0.00, ATATATACATATATATATA=0.00, ATATATACATATATATATATA=0.00, ATATATACATATATATATATATA=0.00, ATATATACATATATATATATATATA=0.00 1.0 0.0 0.0 N/A
Other Sub 466 ATATATA=1.000 ATATATACATACATATATATATATA=0.000, ATATATACATATATATA=0.000, ATATATACATATATATATA=0.000, ATATATACATATATATATATA=0.000, ATATATACATATATATATATATA=0.000, ATATATACATATATATATATATATA=0.000 1.0 0.0 0.0 N/A


Help

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

Download
Study Population Group Sample Size Ref Allele Alt Allele
14KJPN JAPANESE Study-wide 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
Help

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
Help

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
Help

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
Help

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)
Help

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)
Help

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

Help

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.

Software version is: 2.0.1.post820+afb47a3d