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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.

rs1463275980

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr17:59028669 (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
A>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.000004 (1/251028, GnomAD_exome)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TRIM37 : Missense Variant
Publications
0 citations
Genomic View
See rs on genome
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
gnomAD - Exomes Global Study-wide 251028 A=0.999996 C=0.000004
gnomAD - Exomes European Sub 135058 A=1.000000 C=0.000000
gnomAD - Exomes Asian Sub 49002 A=0.99998 C=0.00002
gnomAD - Exomes American Sub 34576 A=1.00000 C=0.00000
gnomAD - Exomes African Sub 16196 A=1.00000 C=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10074 A=1.00000 C=0.00000
gnomAD - Exomes Other Sub 6122 A=1.0000 C=0.0000
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 17 NC_000017.11:g.59028669A>C
GRCh37.p13 chr 17 NC_000017.10:g.57106030A>C
TRIM37 RefSeqGene NG_009298.1:g.83237T>G
Gene: TRIM37, tripartite motif containing 37 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
TRIM37 transcript variant 1 NM_015294.6:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform a NP_056109.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant 10 NM_001353083.2:c.1268T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform f NP_001340012.1:p.Val423Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant 5 NM_001320989.3:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform c NP_001307918.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant 12 NM_001353085.2:c.1541T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform h NP_001340014.1:p.Val514Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant 7 NM_001353082.2:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform e NP_001340011.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant 6 NM_001320990.3:c.1637T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform d NP_001307919.1:p.Val546Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant 13 NM_001353086.2:c.1952T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform i NP_001340015.1:p.Val651Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant 4 NM_001320988.3:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform c NP_001307917.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant 3 NM_001320987.3:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform b NP_001307916.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant 2 NM_001005207.5:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform a NP_001005207.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant 11 NM_001353084.2:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform g NP_001340013.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant 9 NR_148347.2:n.2320T>G N/A Non Coding Transcript Variant
TRIM37 transcript variant 8 NR_148346.2:n.2422T>G N/A Non Coding Transcript Variant
TRIM37 transcript variant X1 XM_011524831.2:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X1 XP_011523133.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X2 XM_017024662.2:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X2 XP_016880151.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X3 XM_011524832.3:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X3 XP_011523134.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X4 XM_017024663.3:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X4 XP_016880152.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X5 XM_011524833.2:c.1952T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X5 XP_011523135.1:p.Val651Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X6 XM_005257385.2:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X6 XP_005257442.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X7 XM_047436106.1:c.1952T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X7 XP_047292062.1:p.Val651Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X8 XM_011524834.2:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X8 XP_011523136.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X9 XM_047436107.1:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X9 XP_047292063.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X10 XM_047436108.1:c.1952T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X10 XP_047292064.1:p.Val651Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X11 XM_017024665.2:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X11 XP_016880154.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X12 XM_047436109.1:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X12 XP_047292065.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X13 XM_047436110.1:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X13 XP_047292066.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X14 XM_011524836.2:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X14 XP_011523138.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X15 XM_047436111.1:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X15 XP_047292067.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X16 XM_017024667.2:c.1952T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X16 XP_016880156.1:p.Val651Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X17 XM_047436112.1:c.1850T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X17 XP_047292068.1:p.Val617Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X18 XM_047436113.1:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X18 XP_047292069.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X19 XM_047436114.1:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X19 XP_047292070.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X20 XM_047436115.1:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X20 XP_047292071.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X21 XM_047436116.1:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X21 XP_047292072.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X22 XM_017024669.3:c.1850T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X22 XP_016880158.1:p.Val617Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X23 XM_047436117.1:c.1952T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X23 XP_047292073.1:p.Val651Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X24 XM_047436118.1:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X24 XP_047292074.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X25 XM_047436119.1:c.1952T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X25 XP_047292075.1:p.Val651Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X26 XM_047436120.1:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X26 XP_047292076.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X27 XM_017024670.3:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X27 XP_016880159.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X28 XM_047436121.1:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X28 XP_047292077.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X29 XM_047436122.1:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X29 XP_047292078.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X30 XM_047436123.1:c.2003T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X30 XP_047292079.1:p.Val668Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X31 XM_047436124.1:c.1850T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X31 XP_047292080.1:p.Val617Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X32 XM_047436125.1:c.1850T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X32 XP_047292081.1:p.Val617Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X33 XM_047436126.1:c.1901T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X33 XP_047292082.1:p.Val634Gly V (Val) > G (Gly) Missense Variant
TRIM37 transcript variant X34 XM_017024673.3:c.1268T>G V [GTG] > G [GGG] Coding Sequence Variant
E3 ubiquitin-protein ligase TRIM37 isoform X34 XP_016880162.1:p.Val423Gly V (Val) > G (Gly) Missense 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 A= C
GRCh38.p14 chr 17 NC_000017.11:g.59028669= NC_000017.11:g.59028669A>C
GRCh37.p13 chr 17 NC_000017.10:g.57106030= NC_000017.10:g.57106030A>C
TRIM37 RefSeqGene NG_009298.1:g.83237= NG_009298.1:g.83237T>G
TRIM37 transcript variant 1 NM_015294.6:c.2003= NM_015294.6:c.2003T>G
TRIM37 transcript variant 1 NM_015294.5:c.2003= NM_015294.5:c.2003T>G
TRIM37 transcript variant 1 NM_015294.4:c.2003= NM_015294.4:c.2003T>G
TRIM37 transcript variant 1 NM_015294.3:c.2003= NM_015294.3:c.2003T>G
TRIM37 transcript variant 2 NM_001005207.5:c.2003= NM_001005207.5:c.2003T>G
TRIM37 transcript variant 2 NM_001005207.4:c.2003= NM_001005207.4:c.2003T>G
TRIM37 transcript variant 2 NM_001005207.3:c.2003= NM_001005207.3:c.2003T>G
TRIM37 transcript variant 2 NM_001005207.2:c.2003= NM_001005207.2:c.2003T>G
TRIM37 transcript variant 6 NM_001320990.3:c.1637= NM_001320990.3:c.1637T>G
TRIM37 transcript variant 6 NM_001320990.2:c.1637= NM_001320990.2:c.1637T>G
TRIM37 transcript variant 6 NM_001320990.1:c.1637= NM_001320990.1:c.1637T>G
TRIM37 transcript variant 3 NM_001320987.3:c.1901= NM_001320987.3:c.1901T>G
TRIM37 transcript variant 3 NM_001320987.2:c.1901= NM_001320987.2:c.1901T>G
TRIM37 transcript variant 3 NM_001320987.1:c.1901= NM_001320987.1:c.1901T>G
TRIM37 transcript variant 4 NM_001320988.3:c.2003= NM_001320988.3:c.2003T>G
TRIM37 transcript variant 4 NM_001320988.2:c.2003= NM_001320988.2:c.2003T>G
TRIM37 transcript variant 4 NM_001320988.1:c.2003= NM_001320988.1:c.2003T>G
TRIM37 transcript variant 5 NM_001320989.3:c.2003= NM_001320989.3:c.2003T>G
TRIM37 transcript variant 5 NM_001320989.2:c.2003= NM_001320989.2:c.2003T>G
TRIM37 transcript variant 5 NM_001320989.1:c.2003= NM_001320989.1:c.2003T>G
TRIM37 transcript variant 8 NR_148346.2:n.2422= NR_148346.2:n.2422T>G
TRIM37 transcript variant 8 NR_148346.1:n.2506= NR_148346.1:n.2506T>G
TRIM37 transcript variant 11 NM_001353084.2:c.2003= NM_001353084.2:c.2003T>G
TRIM37 transcript variant 11 NM_001353084.1:c.2003= NM_001353084.1:c.2003T>G
TRIM37 transcript variant 10 NM_001353083.2:c.1268= NM_001353083.2:c.1268T>G
TRIM37 transcript variant 10 NM_001353083.1:c.1268= NM_001353083.1:c.1268T>G
TRIM37 transcript variant 13 NM_001353086.2:c.1952= NM_001353086.2:c.1952T>G
TRIM37 transcript variant 13 NM_001353086.1:c.1952= NM_001353086.1:c.1952T>G
TRIM37 transcript variant 9 NR_148347.2:n.2320= NR_148347.2:n.2320T>G
TRIM37 transcript variant 9 NR_148347.1:n.2404= NR_148347.1:n.2404T>G
TRIM37 transcript variant 7 NM_001353082.2:c.1901= NM_001353082.2:c.1901T>G
TRIM37 transcript variant 7 NM_001353082.1:c.1901= NM_001353082.1:c.1901T>G
TRIM37 transcript variant 12 NM_001353085.2:c.1541= NM_001353085.2:c.1541T>G
TRIM37 transcript variant 12 NM_001353085.1:c.1541= NM_001353085.1:c.1541T>G
TRIM37 transcript variant X3 XM_011524832.3:c.2003= XM_011524832.3:c.2003T>G
TRIM37 transcript variant X3 XM_011524832.2:c.2003= XM_011524832.2:c.2003T>G
TRIM37 transcript variant X2 XM_011524832.1:c.2003= XM_011524832.1:c.2003T>G
TRIM37 transcript variant X4 XM_017024663.3:c.2003= XM_017024663.3:c.2003T>G
TRIM37 transcript variant X4 XM_017024663.2:c.2003= XM_017024663.2:c.2003T>G
TRIM37 transcript variant X4 XM_017024663.1:c.2003= XM_017024663.1:c.2003T>G
TRIM37 transcript variant X22 XM_017024669.3:c.1850= XM_017024669.3:c.1850T>G
TRIM37 transcript variant X12 XM_017024669.2:c.1850= XM_017024669.2:c.1850T>G
TRIM37 transcript variant X15 XM_017024669.1:c.1850= XM_017024669.1:c.1850T>G
TRIM37 transcript variant X27 XM_017024670.3:c.1901= XM_017024670.3:c.1901T>G
TRIM37 transcript variant X13 XM_017024670.2:c.1901= XM_017024670.2:c.1901T>G
TRIM37 transcript variant X16 XM_017024670.1:c.1901= XM_017024670.1:c.1901T>G
TRIM37 transcript variant X34 XM_017024673.3:c.1268= XM_017024673.3:c.1268T>G
TRIM37 transcript variant X17 XM_017024673.2:c.1268= XM_017024673.2:c.1268T>G
TRIM37 transcript variant X20 XM_017024673.1:c.1268= XM_017024673.1:c.1268T>G
TRIM37 transcript variant X2 XM_017024662.2:c.2003= XM_017024662.2:c.2003T>G
TRIM37 transcript variant X2 XM_017024662.1:c.2003= XM_017024662.1:c.2003T>G
TRIM37 transcript variant X1 XM_011524831.2:c.2003= XM_011524831.2:c.2003T>G
TRIM37 transcript variant X1 XM_011524831.1:c.2003= XM_011524831.1:c.2003T>G
TRIM37 transcript variant X11 XM_017024665.2:c.1901= XM_017024665.2:c.1901T>G
TRIM37 transcript variant X9 XM_017024665.1:c.1901= XM_017024665.1:c.1901T>G
TRIM37 transcript variant X14 XM_011524836.2:c.2003= XM_011524836.2:c.2003T>G
TRIM37 transcript variant X10 XM_011524836.1:c.2003= XM_011524836.1:c.2003T>G
TRIM37 transcript variant X6 XM_005257385.2:c.2003= XM_005257385.2:c.2003T>G
TRIM37 transcript variant X6 XM_005257385.1:c.2003= XM_005257385.1:c.2003T>G
TRIM37 transcript variant X16 XM_017024667.2:c.1952= XM_017024667.2:c.1952T>G
TRIM37 transcript variant X11 XM_017024667.1:c.1952= XM_017024667.1:c.1952T>G
TRIM37 transcript variant X5 XM_011524833.2:c.1952= XM_011524833.2:c.1952T>G
TRIM37 transcript variant X5 XM_011524833.1:c.1952= XM_011524833.1:c.1952T>G
TRIM37 transcript variant X8 XM_011524834.2:c.1901= XM_011524834.2:c.1901T>G
TRIM37 transcript variant X7 XM_011524834.1:c.1901= XM_011524834.1:c.1901T>G
TRIM37 transcript variant X9 XM_047436107.1:c.1901= XM_047436107.1:c.1901T>G
TRIM37 transcript variant X13 XM_047436110.1:c.1901= XM_047436110.1:c.1901T>G
TRIM37 transcript variant X15 XM_047436111.1:c.2003= XM_047436111.1:c.2003T>G
TRIM37 transcript variant X7 XM_047436106.1:c.1952= XM_047436106.1:c.1952T>G
TRIM37 transcript variant X12 XM_047436109.1:c.2003= XM_047436109.1:c.2003T>G
TRIM37 transcript variant X25 XM_047436119.1:c.1952= XM_047436119.1:c.1952T>G
TRIM37 transcript variant X26 XM_047436120.1:c.1901= XM_047436120.1:c.1901T>G
TRIM37 transcript variant X31 XM_047436124.1:c.1850= XM_047436124.1:c.1850T>G
TRIM37 transcript variant X32 XM_047436125.1:c.1850= XM_047436125.1:c.1850T>G
TRIM37 transcript variant X33 XM_047436126.1:c.1901= XM_047436126.1:c.1901T>G
TRIM37 transcript variant X10 XM_047436108.1:c.1952= XM_047436108.1:c.1952T>G
TRIM37 transcript variant X18 XM_047436113.1:c.1901= XM_047436113.1:c.1901T>G
TRIM37 transcript variant X20 XM_047436115.1:c.2003= XM_047436115.1:c.2003T>G
TRIM37 transcript variant X19 XM_047436114.1:c.1901= XM_047436114.1:c.1901T>G
TRIM37 transcript variant X21 XM_047436116.1:c.2003= XM_047436116.1:c.2003T>G
TRIM37 transcript variant X23 XM_047436117.1:c.1952= XM_047436117.1:c.1952T>G
TRIM37 transcript variant X28 XM_047436121.1:c.1901= XM_047436121.1:c.1901T>G
TRIM37 transcript variant X29 XM_047436122.1:c.1901= XM_047436122.1:c.1901T>G
TRIM37 transcript variant X30 XM_047436123.1:c.2003= XM_047436123.1:c.2003T>G
TRIM37 transcript variant X17 XM_047436112.1:c.1850= XM_047436112.1:c.1850T>G
TRIM37 transcript variant X24 XM_047436118.1:c.2003= XM_047436118.1:c.2003T>G
E3 ubiquitin-protein ligase TRIM37 isoform a NP_056109.1:p.Val668= NP_056109.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform a NP_001005207.1:p.Val668= NP_001005207.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform d NP_001307919.1:p.Val546= NP_001307919.1:p.Val546Gly
E3 ubiquitin-protein ligase TRIM37 isoform b NP_001307916.1:p.Val634= NP_001307916.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform c NP_001307917.1:p.Val668= NP_001307917.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform c NP_001307918.1:p.Val668= NP_001307918.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform g NP_001340013.1:p.Val668= NP_001340013.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform f NP_001340012.1:p.Val423= NP_001340012.1:p.Val423Gly
E3 ubiquitin-protein ligase TRIM37 isoform i NP_001340015.1:p.Val651= NP_001340015.1:p.Val651Gly
E3 ubiquitin-protein ligase TRIM37 isoform e NP_001340011.1:p.Val634= NP_001340011.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform h NP_001340014.1:p.Val514= NP_001340014.1:p.Val514Gly
E3 ubiquitin-protein ligase TRIM37 isoform X3 XP_011523134.1:p.Val668= XP_011523134.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform X4 XP_016880152.1:p.Val668= XP_016880152.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform X22 XP_016880158.1:p.Val617= XP_016880158.1:p.Val617Gly
E3 ubiquitin-protein ligase TRIM37 isoform X27 XP_016880159.1:p.Val634= XP_016880159.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform X34 XP_016880162.1:p.Val423= XP_016880162.1:p.Val423Gly
E3 ubiquitin-protein ligase TRIM37 isoform X2 XP_016880151.1:p.Val668= XP_016880151.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform X1 XP_011523133.1:p.Val668= XP_011523133.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform X11 XP_016880154.1:p.Val634= XP_016880154.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform X14 XP_011523138.1:p.Val668= XP_011523138.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform X6 XP_005257442.1:p.Val668= XP_005257442.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform X16 XP_016880156.1:p.Val651= XP_016880156.1:p.Val651Gly
E3 ubiquitin-protein ligase TRIM37 isoform X5 XP_011523135.1:p.Val651= XP_011523135.1:p.Val651Gly
E3 ubiquitin-protein ligase TRIM37 isoform X8 XP_011523136.1:p.Val634= XP_011523136.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform X9 XP_047292063.1:p.Val634= XP_047292063.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform X13 XP_047292066.1:p.Val634= XP_047292066.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform X15 XP_047292067.1:p.Val668= XP_047292067.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform X7 XP_047292062.1:p.Val651= XP_047292062.1:p.Val651Gly
E3 ubiquitin-protein ligase TRIM37 isoform X12 XP_047292065.1:p.Val668= XP_047292065.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform X25 XP_047292075.1:p.Val651= XP_047292075.1:p.Val651Gly
E3 ubiquitin-protein ligase TRIM37 isoform X26 XP_047292076.1:p.Val634= XP_047292076.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform X31 XP_047292080.1:p.Val617= XP_047292080.1:p.Val617Gly
E3 ubiquitin-protein ligase TRIM37 isoform X32 XP_047292081.1:p.Val617= XP_047292081.1:p.Val617Gly
E3 ubiquitin-protein ligase TRIM37 isoform X33 XP_047292082.1:p.Val634= XP_047292082.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform X10 XP_047292064.1:p.Val651= XP_047292064.1:p.Val651Gly
E3 ubiquitin-protein ligase TRIM37 isoform X18 XP_047292069.1:p.Val634= XP_047292069.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform X20 XP_047292071.1:p.Val668= XP_047292071.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform X19 XP_047292070.1:p.Val634= XP_047292070.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform X21 XP_047292072.1:p.Val668= XP_047292072.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform X23 XP_047292073.1:p.Val651= XP_047292073.1:p.Val651Gly
E3 ubiquitin-protein ligase TRIM37 isoform X28 XP_047292077.1:p.Val634= XP_047292077.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform X29 XP_047292078.1:p.Val634= XP_047292078.1:p.Val634Gly
E3 ubiquitin-protein ligase TRIM37 isoform X30 XP_047292079.1:p.Val668= XP_047292079.1:p.Val668Gly
E3 ubiquitin-protein ligase TRIM37 isoform X17 XP_047292068.1:p.Val617= XP_047292068.1:p.Val617Gly
E3 ubiquitin-protein ligase TRIM37 isoform X24 XP_047292074.1:p.Val668= XP_047292074.1:p.Val668Gly
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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#.

1 SubSNP, 1 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2742884600 Nov 08, 2017 (151)
2 gnomAD - Exomes NC_000017.10 - 57106030 Jul 13, 2019 (153)
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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
12189674, ss2742884600 NC_000017.10:57106029:A:C NC_000017.11:59028668:A:C (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1463275980

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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.

Software version is: 2.0.1.post820+afb47a3d