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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs1451944480

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr17:68385091 (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
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.000004 (1/251214, GnomAD_exome)
A=0.00000 (0/10680, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ARSG : Stop Gained
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 10680 G=1.00000 A=0.00000 1.0 0.0 0.0 N/A
European Sub 6962 G=1.0000 A=0.0000 1.0 0.0 0.0 N/A
African Sub 2294 G=1.0000 A=0.0000 1.0 0.0 0.0 N/A
African Others Sub 84 G=1.00 A=0.00 1.0 0.0 0.0 N/A
African American Sub 2210 G=1.0000 A=0.0000 1.0 0.0 0.0 N/A
Asian Sub 108 G=1.000 A=0.000 1.0 0.0 0.0 N/A
East Asian Sub 84 G=1.00 A=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 24 G=1.00 A=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 G=1.000 A=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 G=1.000 A=0.000 1.0 0.0 0.0 N/A
South Asian Sub 94 G=1.00 A=0.00 1.0 0.0 0.0 N/A
Other Sub 466 G=1.000 A=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
gnomAD - Exomes Global Study-wide 251214 G=0.999996 A=0.000004
gnomAD - Exomes European Sub 135172 G=0.999993 A=0.000007
gnomAD - Exomes Asian Sub 49010 G=1.00000 A=0.00000
gnomAD - Exomes American Sub 34590 G=1.00000 A=0.00000
gnomAD - Exomes African Sub 16252 G=1.00000 A=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10066 G=1.00000 A=0.00000
gnomAD - Exomes Other Sub 6124 G=1.0000 A=0.0000
Allele Frequency Aggregator Total Global 10680 G=1.00000 A=0.00000
Allele Frequency Aggregator European Sub 6962 G=1.0000 A=0.0000
Allele Frequency Aggregator African Sub 2294 G=1.0000 A=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 G=1.000 A=0.000
Allele Frequency Aggregator Other Sub 466 G=1.000 A=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 G=1.000 A=0.000
Allele Frequency Aggregator Asian Sub 108 G=1.000 A=0.000
Allele Frequency Aggregator South Asian Sub 94 G=1.00 A=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 17 NC_000017.11:g.68385091G>A
GRCh37.p13 chr 17 NC_000017.10:g.66381232G>A
ARSG RefSeqGene NG_032814.2:g.131003G>A
Gene: ARSG, arylsulfatase G (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ARSG transcript variant 9 NM_001352905.2:c.1007G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 2 precursor NP_001339834.1:p.Trp336Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 7 NM_001352903.2:c.1007G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 2 precursor NP_001339832.1:p.Trp336Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 11 NM_001352907.2:c.1007G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 2 precursor NP_001339836.1:p.Trp336Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 6 NM_001352902.2:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 1 precursor NP_001339831.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 5 NM_001352901.2:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 1 precursor NP_001339830.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 4 NM_001352900.2:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 1 precursor NP_001339829.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 12 NM_001352909.2:c.962G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 3 NP_001339838.1:p.Trp321Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 13 NM_001352910.2:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 4 precursor NP_001339839.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 1 NM_014960.5:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 1 precursor NP_055775.2:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 2 NM_001267727.2:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 1 precursor NP_001254656.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 8 NM_001352904.2:c.1007G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 2 precursor NP_001339833.1:p.Trp336Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 3 NM_001352899.2:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 1 precursor NP_001339828.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant 10 NM_001352906.2:c.1007G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform 2 precursor NP_001339835.1:p.Trp336Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X26 XM_047435651.1:c. N/A Genic Downstream Transcript Variant
ARSG transcript variant X27 XM_047435652.1:c. N/A Genic Downstream Transcript Variant
ARSG transcript variant X29 XM_047435653.1:c. N/A Genic Downstream Transcript Variant
ARSG transcript variant X30 XM_047435654.1:c. N/A Genic Downstream Transcript Variant
ARSG transcript variant X31 XM_047435655.1:c. N/A Genic Downstream Transcript Variant
ARSG transcript variant X1 XM_011524536.3:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X1 XP_011522838.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X2 XM_047435632.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X1 XP_047291588.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X3 XM_017024360.3:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X1 XP_016879849.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X4 XM_011524537.2:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X1 XP_011522839.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X5 XM_047435633.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X1 XP_047291589.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X6 XM_047435634.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X1 XP_047291590.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X7 XM_047435635.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X1 XP_047291591.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X8 XM_047435636.1:c.1007G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X2 XP_047291592.1:p.Trp336Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X9 XM_047435637.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X3 XP_047291593.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X10 XM_047435638.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X4 XP_047291594.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X11 XM_047435639.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X4 XP_047291595.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X12 XM_047435640.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X4 XP_047291596.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X13 XM_017024365.2:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X4 XP_016879854.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X14 XM_047435641.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X5 XP_047291597.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X15 XM_047435642.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X6 XP_047291598.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X16 XM_047435643.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X6 XP_047291599.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X17 XM_047435644.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X7 XP_047291600.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X18 XM_047435645.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X7 XP_047291601.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X19 XM_047435646.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X7 XP_047291602.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X20 XM_017024368.2:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X8 XP_016879857.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X22 XM_047435647.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X6 XP_047291603.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X23 XM_047435648.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X8 XP_047291604.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X24 XM_047435649.1:c.1010G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X8 XP_047291605.1:p.Trp337Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X25 XM_047435650.1:c.518G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X9 XP_047291606.1:p.Trp173Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X28 XM_011524546.3:c.263G>A W [TGG] > * [TAG] Coding Sequence Variant
arylsulfatase G isoform X12 XP_011522848.1:p.Trp88Ter W (Trp) > * (Ter) Stop Gained
ARSG transcript variant X21 XR_007065287.1:n.1635G>A N/A Non Coding 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 G= A
GRCh38.p14 chr 17 NC_000017.11:g.68385091= NC_000017.11:g.68385091G>A
GRCh37.p13 chr 17 NC_000017.10:g.66381232= NC_000017.10:g.66381232G>A
ARSG RefSeqGene NG_032814.2:g.131003= NG_032814.2:g.131003G>A
ARSG transcript variant 1 NM_014960.5:c.1010= NM_014960.5:c.1010G>A
ARSG transcript variant 1 NM_014960.4:c.1010= NM_014960.4:c.1010G>A
ARSG transcript variant 7 NM_001352903.2:c.1007= NM_001352903.2:c.1007G>A
ARSG transcript variant 7 NM_001352903.1:c.1007= NM_001352903.1:c.1007G>A
ARSG transcript variant 4 NM_001352900.2:c.1010= NM_001352900.2:c.1010G>A
ARSG transcript variant 4 NM_001352900.1:c.1010= NM_001352900.1:c.1010G>A
ARSG transcript variant 5 NM_001352901.2:c.1010= NM_001352901.2:c.1010G>A
ARSG transcript variant 5 NM_001352901.1:c.1010= NM_001352901.1:c.1010G>A
ARSG transcript variant 11 NM_001352907.2:c.1007= NM_001352907.2:c.1007G>A
ARSG transcript variant 11 NM_001352907.1:c.1007= NM_001352907.1:c.1007G>A
ARSG transcript variant 13 NM_001352910.2:c.1010= NM_001352910.2:c.1010G>A
ARSG transcript variant 13 NM_001352910.1:c.1010= NM_001352910.1:c.1010G>A
ARSG transcript variant 6 NM_001352902.2:c.1010= NM_001352902.2:c.1010G>A
ARSG transcript variant 6 NM_001352902.1:c.1010= NM_001352902.1:c.1010G>A
ARSG transcript variant 8 NM_001352904.2:c.1007= NM_001352904.2:c.1007G>A
ARSG transcript variant 8 NM_001352904.1:c.1007= NM_001352904.1:c.1007G>A
ARSG transcript variant 9 NM_001352905.2:c.1007= NM_001352905.2:c.1007G>A
ARSG transcript variant 9 NM_001352905.1:c.1007= NM_001352905.1:c.1007G>A
ARSG transcript variant 3 NM_001352899.2:c.1010= NM_001352899.2:c.1010G>A
ARSG transcript variant 3 NM_001352899.1:c.1010= NM_001352899.1:c.1010G>A
ARSG transcript variant 10 NM_001352906.2:c.1007= NM_001352906.2:c.1007G>A
ARSG transcript variant 10 NM_001352906.1:c.1007= NM_001352906.1:c.1007G>A
ARSG transcript variant 12 NM_001352909.2:c.962= NM_001352909.2:c.962G>A
ARSG transcript variant 12 NM_001352909.1:c.962= NM_001352909.1:c.962G>A
ARSG transcript variant 2 NM_001267727.2:c.1010= NM_001267727.2:c.1010G>A
ARSG transcript variant 2 NM_001267727.1:c.1010= NM_001267727.1:c.1010G>A
ARSG transcript variant X3 XM_017024360.3:c.1010= XM_017024360.3:c.1010G>A
ARSG transcript variant X2 XM_017024360.2:c.1010= XM_017024360.2:c.1010G>A
ARSG transcript variant X6 XM_017024360.1:c.1010= XM_017024360.1:c.1010G>A
ARSG transcript variant X1 XM_011524536.3:c.1010= XM_011524536.3:c.1010G>A
ARSG transcript variant X1 XM_011524536.2:c.1010= XM_011524536.2:c.1010G>A
ARSG transcript variant X2 XM_011524536.1:c.1010= XM_011524536.1:c.1010G>A
ARSG transcript variant X28 XM_011524546.3:c.263= XM_011524546.3:c.263G>A
ARSG transcript variant X7 XM_011524546.2:c.263= XM_011524546.2:c.263G>A
ARSG transcript variant X17 XM_011524546.1:c.263= XM_011524546.1:c.263G>A
ARSG transcript variant X4 XM_011524537.2:c.1010= XM_011524537.2:c.1010G>A
ARSG transcript variant X3 XM_011524537.1:c.1010= XM_011524537.1:c.1010G>A
ARSG transcript variant X20 XM_017024368.2:c.1010= XM_017024368.2:c.1010G>A
ARSG transcript variant X6 XM_017024368.1:c.1010= XM_017024368.1:c.1010G>A
ARSG transcript variant X13 XM_017024365.2:c.1010= XM_017024365.2:c.1010G>A
ARSG transcript variant X4 XM_017024365.1:c.1010= XM_017024365.1:c.1010G>A
ARSG transcript variant X7 XM_047435635.1:c.1010= XM_047435635.1:c.1010G>A
ARSG transcript variant X2 XM_047435632.1:c.1010= XM_047435632.1:c.1010G>A
ARSG transcript variant X10 XM_047435638.1:c.1010= XM_047435638.1:c.1010G>A
ARSG transcript variant X8 XM_047435636.1:c.1007= XM_047435636.1:c.1007G>A
ARSG transcript variant X24 XM_047435649.1:c.1010= XM_047435649.1:c.1010G>A
ARSG transcript variant X23 XM_047435648.1:c.1010= XM_047435648.1:c.1010G>A
ARSG transcript variant X25 XM_047435650.1:c.518= XM_047435650.1:c.518G>A
ARSG transcript variant X17 XM_047435644.1:c.1010= XM_047435644.1:c.1010G>A
ARSG transcript variant X22 XM_047435647.1:c.1010= XM_047435647.1:c.1010G>A
ARSG transcript variant X16 XM_047435643.1:c.1010= XM_047435643.1:c.1010G>A
ARSG transcript variant X11 XM_047435639.1:c.1010= XM_047435639.1:c.1010G>A
ARSG transcript variant X6 XM_047435634.1:c.1010= XM_047435634.1:c.1010G>A
ARSG transcript variant X19 XM_047435646.1:c.1010= XM_047435646.1:c.1010G>A
ARSG transcript variant X5 XM_047435633.1:c.1010= XM_047435633.1:c.1010G>A
ARSG transcript variant X12 XM_047435640.1:c.1010= XM_047435640.1:c.1010G>A
ARSG transcript variant X18 XM_047435645.1:c.1010= XM_047435645.1:c.1010G>A
ARSG transcript variant X14 XM_047435641.1:c.1010= XM_047435641.1:c.1010G>A
ARSG transcript variant X21 XR_007065287.1:n.1635= XR_007065287.1:n.1635G>A
ARSG transcript variant X9 XM_047435637.1:c.1010= XM_047435637.1:c.1010G>A
ARSG transcript variant X15 XM_047435642.1:c.1010= XM_047435642.1:c.1010G>A
arylsulfatase G isoform 1 precursor NP_055775.2:p.Trp337= NP_055775.2:p.Trp337Ter
arylsulfatase G isoform 2 precursor NP_001339832.1:p.Trp336= NP_001339832.1:p.Trp336Ter
arylsulfatase G isoform 1 precursor NP_001339829.1:p.Trp337= NP_001339829.1:p.Trp337Ter
arylsulfatase G isoform 1 precursor NP_001339830.1:p.Trp337= NP_001339830.1:p.Trp337Ter
arylsulfatase G isoform 2 precursor NP_001339836.1:p.Trp336= NP_001339836.1:p.Trp336Ter
arylsulfatase G isoform 4 precursor NP_001339839.1:p.Trp337= NP_001339839.1:p.Trp337Ter
arylsulfatase G isoform 1 precursor NP_001339831.1:p.Trp337= NP_001339831.1:p.Trp337Ter
arylsulfatase G isoform 2 precursor NP_001339833.1:p.Trp336= NP_001339833.1:p.Trp336Ter
arylsulfatase G isoform 2 precursor NP_001339834.1:p.Trp336= NP_001339834.1:p.Trp336Ter
arylsulfatase G isoform 1 precursor NP_001339828.1:p.Trp337= NP_001339828.1:p.Trp337Ter
arylsulfatase G isoform 2 precursor NP_001339835.1:p.Trp336= NP_001339835.1:p.Trp336Ter
arylsulfatase G isoform 3 NP_001339838.1:p.Trp321= NP_001339838.1:p.Trp321Ter
arylsulfatase G isoform 1 precursor NP_001254656.1:p.Trp337= NP_001254656.1:p.Trp337Ter
arylsulfatase G isoform X1 XP_016879849.1:p.Trp337= XP_016879849.1:p.Trp337Ter
arylsulfatase G isoform X1 XP_011522838.1:p.Trp337= XP_011522838.1:p.Trp337Ter
arylsulfatase G isoform X12 XP_011522848.1:p.Trp88= XP_011522848.1:p.Trp88Ter
arylsulfatase G isoform X1 XP_011522839.1:p.Trp337= XP_011522839.1:p.Trp337Ter
arylsulfatase G isoform X8 XP_016879857.1:p.Trp337= XP_016879857.1:p.Trp337Ter
arylsulfatase G isoform X4 XP_016879854.1:p.Trp337= XP_016879854.1:p.Trp337Ter
arylsulfatase G isoform X1 XP_047291591.1:p.Trp337= XP_047291591.1:p.Trp337Ter
arylsulfatase G isoform X1 XP_047291588.1:p.Trp337= XP_047291588.1:p.Trp337Ter
arylsulfatase G isoform X4 XP_047291594.1:p.Trp337= XP_047291594.1:p.Trp337Ter
arylsulfatase G isoform X2 XP_047291592.1:p.Trp336= XP_047291592.1:p.Trp336Ter
arylsulfatase G isoform X8 XP_047291605.1:p.Trp337= XP_047291605.1:p.Trp337Ter
arylsulfatase G isoform X8 XP_047291604.1:p.Trp337= XP_047291604.1:p.Trp337Ter
arylsulfatase G isoform X9 XP_047291606.1:p.Trp173= XP_047291606.1:p.Trp173Ter
arylsulfatase G isoform X7 XP_047291600.1:p.Trp337= XP_047291600.1:p.Trp337Ter
arylsulfatase G isoform X6 XP_047291603.1:p.Trp337= XP_047291603.1:p.Trp337Ter
arylsulfatase G isoform X6 XP_047291599.1:p.Trp337= XP_047291599.1:p.Trp337Ter
arylsulfatase G isoform X4 XP_047291595.1:p.Trp337= XP_047291595.1:p.Trp337Ter
arylsulfatase G isoform X1 XP_047291590.1:p.Trp337= XP_047291590.1:p.Trp337Ter
arylsulfatase G isoform X7 XP_047291602.1:p.Trp337= XP_047291602.1:p.Trp337Ter
arylsulfatase G isoform X1 XP_047291589.1:p.Trp337= XP_047291589.1:p.Trp337Ter
arylsulfatase G isoform X4 XP_047291596.1:p.Trp337= XP_047291596.1:p.Trp337Ter
arylsulfatase G isoform X7 XP_047291601.1:p.Trp337= XP_047291601.1:p.Trp337Ter
arylsulfatase G isoform X5 XP_047291597.1:p.Trp337= XP_047291597.1:p.Trp337Ter
arylsulfatase G isoform X3 XP_047291593.1:p.Trp337= XP_047291593.1:p.Trp337Ter
arylsulfatase G isoform X6 XP_047291598.1:p.Trp337= XP_047291598.1:p.Trp337Ter
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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, 2 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2742955469 Nov 08, 2017 (151)
2 gnomAD - Exomes NC_000017.10 - 66381232 Jul 13, 2019 (153)
3 ALFA NC_000017.11 - 68385091 Apr 27, 2021 (155)
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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
12262681, ss2742955469 NC_000017.10:66381231:G:A NC_000017.11:68385090:G:A (self)
13869138861 NC_000017.11:68385090:G:A NC_000017.11:68385090:G:A (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 rs1451944480

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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