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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.

rs1482674282

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr10:48454159 (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 / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.000004 (1/251338, GnomAD_exome)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ARHGAP22 : 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 251338 G=0.999996 T=0.000004
gnomAD - Exomes European Sub 135310 G=1.000000 T=0.000000
gnomAD - Exomes Asian Sub 49008 G=0.99998 T=0.00002
gnomAD - Exomes American Sub 34576 G=1.00000 T=0.00000
gnomAD - Exomes African Sub 16240 G=1.00000 T=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10070 G=1.00000 T=0.00000
gnomAD - Exomes Other Sub 6134 G=1.0000 T=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 10 NC_000010.11:g.48454159G>A
GRCh38.p14 chr 10 NC_000010.11:g.48454159G>T
GRCh37.p13 chr 10 NC_000010.10:g.49662202G>A
GRCh37.p13 chr 10 NC_000010.10:g.49662202G>T
ARHGAP22 RefSeqGene NG_053158.1:g.207107C>T
ARHGAP22 RefSeqGene NG_053158.1:g.207107C>A
Gene: ARHGAP22, Rho GTPase activating protein 22 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ARHGAP22 transcript variant 8 NM_001347736.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 9 NM_001347737.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant 1 NM_001256024.2:c.843C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 1 NP_001242953.1:p.Gly281= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 1 NM_001256024.2:c.843C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 1 NP_001242953.1:p.Gly281= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 10 NM_001347738.2:c.813C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 2 NP_001334667.1:p.Gly271= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 10 NM_001347738.2:c.813C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 2 NP_001334667.1:p.Gly271= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 2 NM_001256025.3:c.813C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 2 NP_001242954.1:p.Gly271= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 2 NM_001256025.3:c.813C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 2 NP_001242954.1:p.Gly271= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 4 NM_001256026.2:c.525C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 4 NP_001242955.1:p.Gly175= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 4 NM_001256026.2:c.525C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 4 NP_001242955.1:p.Gly175= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 3 NM_021226.4:c.795C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 3 NP_067049.2:p.Gly265= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 3 NM_021226.4:c.795C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 3 NP_067049.2:p.Gly265= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 7 NM_001347735.2:c.666C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 7 NP_001334664.1:p.Gly222= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 7 NM_001347735.2:c.666C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform 7 NP_001334664.1:p.Gly222= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant 13 NR_144644.2:n.943C>T N/A Non Coding Transcript Variant
ARHGAP22 transcript variant 13 NR_144644.2:n.943C>A N/A Non Coding Transcript Variant
ARHGAP22 transcript variant 12 NR_144643.2:n.1072C>T N/A Non Coding Transcript Variant
ARHGAP22 transcript variant 12 NR_144643.2:n.1072C>A N/A Non Coding Transcript Variant
ARHGAP22 transcript variant 15 NR_144646.2:n.864C>T N/A Non Coding Transcript Variant
ARHGAP22 transcript variant 15 NR_144646.2:n.864C>A N/A Non Coding Transcript Variant
ARHGAP22 transcript variant 14 NR_144645.2:n.1020C>T N/A Non Coding Transcript Variant
ARHGAP22 transcript variant 14 NR_144645.2:n.1020C>A N/A Non Coding Transcript Variant
ARHGAP22 transcript variant 11 NR_144642.2:n.1020C>T N/A Non Coding Transcript Variant
ARHGAP22 transcript variant 11 NR_144642.2:n.1020C>A N/A Non Coding Transcript Variant
ARHGAP22 transcript variant 6 NR_045675.2:n.1629C>T N/A Non Coding Transcript Variant
ARHGAP22 transcript variant 6 NR_045675.2:n.1629C>A N/A Non Coding Transcript Variant
ARHGAP22 transcript variant X22 XM_024448102.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X24 XM_024448106.2:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X23 XM_047425595.1:c. N/A Genic Downstream Transcript Variant
ARHGAP22 transcript variant X1 XM_011540002.3:c.861C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X1 XP_011538304.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X1 XM_011540002.3:c.861C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X1 XP_011538304.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X2 XM_024448099.2:c.861C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X1 XP_024303867.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X2 XM_024448099.2:c.861C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X1 XP_024303867.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X3 XM_011540003.2:c.861C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X1 XP_011538305.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X3 XM_011540003.2:c.861C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X1 XP_011538305.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X4 XM_047425586.1:c.813C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X2 XP_047281542.1:p.Gly271= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X4 XM_047425586.1:c.813C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X2 XP_047281542.1:p.Gly271= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X5 XM_047425587.1:c.810C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X3 XP_047281543.1:p.Gly270= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X5 XM_047425587.1:c.810C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X3 XP_047281543.1:p.Gly270= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X6 XM_011540005.2:c.573C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X4 XP_011538307.1:p.Gly191= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X6 XM_011540005.2:c.573C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X4 XP_011538307.1:p.Gly191= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X7 XM_011540006.3:c.684C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X5 XP_011538308.1:p.Gly228= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X7 XM_011540006.3:c.684C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X5 XP_011538308.1:p.Gly228= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X8 XM_005270014.4:c.573C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X6 XP_005270071.1:p.Gly191= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X8 XM_005270014.4:c.573C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X6 XP_005270071.1:p.Gly191= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X9 XM_047425588.1:c.555C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X7 XP_047281544.1:p.Gly185= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X9 XM_047425588.1:c.555C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X7 XP_047281544.1:p.Gly185= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X10 XM_047425589.1:c.525C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X8 XP_047281545.1:p.Gly175= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X10 XM_047425589.1:c.525C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X8 XP_047281545.1:p.Gly175= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X11 XM_047425590.1:c.459C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X9 XP_047281546.1:p.Gly153= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X11 XM_047425590.1:c.459C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X9 XP_047281546.1:p.Gly153= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X12 XM_047425591.1:c.459C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X9 XP_047281547.1:p.Gly153= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X12 XM_047425591.1:c.459C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X9 XP_047281547.1:p.Gly153= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X13 XM_011540011.3:c.396C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X10 XP_011538313.1:p.Gly132= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X13 XM_011540011.3:c.396C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X10 XP_011538313.1:p.Gly132= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X14 XM_017016471.3:c.357C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X11 XP_016871960.1:p.Gly119= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X14 XM_017016471.3:c.357C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X11 XP_016871960.1:p.Gly119= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X15 XM_011540013.4:c.861C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X12 XP_011538315.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X15 XM_011540013.4:c.861C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X12 XP_011538315.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X16 XM_047425592.1:c.861C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X13 XP_047281548.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X16 XM_047425592.1:c.861C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X13 XP_047281548.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X17 XM_024448100.2:c.813C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X14 XP_024303868.1:p.Gly271= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X17 XM_024448100.2:c.813C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X14 XP_024303868.1:p.Gly271= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X18 XM_047425593.1:c.813C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X15 XP_047281549.1:p.Gly271= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X18 XM_047425593.1:c.813C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X15 XP_047281549.1:p.Gly271= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X19 XM_017016476.2:c.795C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X16 XP_016871965.1:p.Gly265= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X19 XM_017016476.2:c.795C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X16 XP_016871965.1:p.Gly265= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X20 XM_011540015.4:c.861C>T G [GGC] > G [GGT] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X17 XP_011538317.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X20 XM_011540015.4:c.861C>A G [GGC] > G [GGA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X17 XP_011538317.1:p.Gly287= G (Gly) > G (Gly) Synonymous Variant
ARHGAP22 transcript variant X21 XM_047425594.1:c.809C>T A [GCA] > V [GTA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X18 XP_047281550.1:p.Ala270Val A (Ala) > V (Val) Missense Variant
ARHGAP22 transcript variant X21 XM_047425594.1:c.809C>A A [GCA] > E [GAA] Coding Sequence Variant
rho GTPase-activating protein 22 isoform X18 XP_047281550.1:p.Ala270Glu A (Ala) > E (Glu) 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 G= A T
GRCh38.p14 chr 10 NC_000010.11:g.48454159= NC_000010.11:g.48454159G>A NC_000010.11:g.48454159G>T
GRCh37.p13 chr 10 NC_000010.10:g.49662202= NC_000010.10:g.49662202G>A NC_000010.10:g.49662202G>T
ARHGAP22 RefSeqGene NG_053158.1:g.207107= NG_053158.1:g.207107C>T NG_053158.1:g.207107C>A
ARHGAP22 transcript variant 3 NM_021226.4:c.795= NM_021226.4:c.795C>T NM_021226.4:c.795C>A
ARHGAP22 transcript variant 3 NM_021226.3:c.795= NM_021226.3:c.795C>T NM_021226.3:c.795C>A
ARHGAP22 transcript variant 2 NM_001256025.3:c.813= NM_001256025.3:c.813C>T NM_001256025.3:c.813C>A
ARHGAP22 transcript variant 2 NM_001256025.2:c.813= NM_001256025.2:c.813C>T NM_001256025.2:c.813C>A
ARHGAP22 transcript variant 6 NR_045675.2:n.1629= NR_045675.2:n.1629C>T NR_045675.2:n.1629C>A
ARHGAP22 transcript variant 6 NR_045675.1:n.1629= NR_045675.1:n.1629C>T NR_045675.1:n.1629C>A
ARHGAP22 transcript variant 12 NR_144643.2:n.1072= NR_144643.2:n.1072C>T NR_144643.2:n.1072C>A
ARHGAP22 transcript variant 12 NR_144643.1:n.1130= NR_144643.1:n.1130C>T NR_144643.1:n.1130C>A
ARHGAP22 transcript variant 11 NR_144642.2:n.1020= NR_144642.2:n.1020C>T NR_144642.2:n.1020C>A
ARHGAP22 transcript variant 11 NR_144642.1:n.1078= NR_144642.1:n.1078C>T NR_144642.1:n.1078C>A
ARHGAP22 transcript variant 13 NR_144644.2:n.943= NR_144644.2:n.943C>T NR_144644.2:n.943C>A
ARHGAP22 transcript variant 13 NR_144644.1:n.1001= NR_144644.1:n.1001C>T NR_144644.1:n.1001C>A
ARHGAP22 transcript variant 10 NM_001347738.2:c.813= NM_001347738.2:c.813C>T NM_001347738.2:c.813C>A
ARHGAP22 transcript variant 10 NM_001347738.1:c.813= NM_001347738.1:c.813C>T NM_001347738.1:c.813C>A
ARHGAP22 transcript variant 1 NM_001256024.2:c.843= NM_001256024.2:c.843C>T NM_001256024.2:c.843C>A
ARHGAP22 transcript variant 1 NM_001256024.1:c.843= NM_001256024.1:c.843C>T NM_001256024.1:c.843C>A
ARHGAP22 transcript variant 14 NR_144645.2:n.1020= NR_144645.2:n.1020C>T NR_144645.2:n.1020C>A
ARHGAP22 transcript variant 14 NR_144645.1:n.1078= NR_144645.1:n.1078C>T NR_144645.1:n.1078C>A
ARHGAP22 transcript variant 7 NM_001347735.2:c.666= NM_001347735.2:c.666C>T NM_001347735.2:c.666C>A
ARHGAP22 transcript variant 7 NM_001347735.1:c.666= NM_001347735.1:c.666C>T NM_001347735.1:c.666C>A
ARHGAP22 transcript variant 15 NR_144646.2:n.864= NR_144646.2:n.864C>T NR_144646.2:n.864C>A
ARHGAP22 transcript variant 15 NR_144646.1:n.922= NR_144646.1:n.922C>T NR_144646.1:n.922C>A
ARHGAP22 transcript variant 4 NM_001256026.2:c.525= NM_001256026.2:c.525C>T NM_001256026.2:c.525C>A
ARHGAP22 transcript variant 4 NM_001256026.1:c.525= NM_001256026.1:c.525C>T NM_001256026.1:c.525C>A
ARHGAP22 transcript variant X15 XM_011540013.4:c.861= XM_011540013.4:c.861C>T XM_011540013.4:c.861C>A
ARHGAP22 transcript variant X10 XM_011540013.3:c.861= XM_011540013.3:c.861C>T XM_011540013.3:c.861C>A
ARHGAP22 transcript variant X13 XM_011540013.2:c.861= XM_011540013.2:c.861C>T XM_011540013.2:c.861C>A
ARHGAP22 transcript variant X13 XM_011540013.1:c.861= XM_011540013.1:c.861C>T XM_011540013.1:c.861C>A
ARHGAP22 transcript variant X20 XM_011540015.4:c.861= XM_011540015.4:c.861C>T XM_011540015.4:c.861C>A
ARHGAP22 transcript variant X16 XM_011540015.3:c.861= XM_011540015.3:c.861C>T XM_011540015.3:c.861C>A
ARHGAP22 transcript variant X23 XM_011540015.2:c.861= XM_011540015.2:c.861C>T XM_011540015.2:c.861C>A
ARHGAP22 transcript variant X15 XM_011540015.1:c.861= XM_011540015.1:c.861C>T XM_011540015.1:c.861C>A
ARHGAP22 transcript variant X8 XM_005270014.4:c.573= XM_005270014.4:c.573C>T XM_005270014.4:c.573C>A
ARHGAP22 transcript variant X6 XM_005270014.3:c.573= XM_005270014.3:c.573C>T XM_005270014.3:c.573C>A
ARHGAP22 transcript variant X7 XM_005270014.2:c.573= XM_005270014.2:c.573C>T XM_005270014.2:c.573C>A
ARHGAP22 transcript variant X2 XM_005270014.1:c.573= XM_005270014.1:c.573C>T XM_005270014.1:c.573C>A
ARHGAP22 transcript variant X1 XM_011540002.3:c.861= XM_011540002.3:c.861C>T XM_011540002.3:c.861C>A
ARHGAP22 transcript variant X1 XM_011540002.2:c.861= XM_011540002.2:c.861C>T XM_011540002.2:c.861C>A
ARHGAP22 transcript variant X1 XM_011540002.1:c.861= XM_011540002.1:c.861C>T XM_011540002.1:c.861C>A
ARHGAP22 transcript variant X7 XM_011540006.3:c.684= XM_011540006.3:c.684C>T XM_011540006.3:c.684C>A
ARHGAP22 transcript variant X5 XM_011540006.2:c.684= XM_011540006.2:c.684C>T XM_011540006.2:c.684C>A
ARHGAP22 transcript variant X5 XM_011540006.1:c.684= XM_011540006.1:c.684C>T XM_011540006.1:c.684C>A
ARHGAP22 transcript variant X14 XM_017016471.3:c.357= XM_017016471.3:c.357C>T XM_017016471.3:c.357C>A
ARHGAP22 transcript variant X9 XM_017016471.2:c.357= XM_017016471.2:c.357C>T XM_017016471.2:c.357C>A
ARHGAP22 transcript variant X11 XM_017016471.1:c.357= XM_017016471.1:c.357C>T XM_017016471.1:c.357C>A
ARHGAP22 transcript variant X13 XM_011540011.3:c.396= XM_011540011.3:c.396C>T XM_011540011.3:c.396C>A
ARHGAP22 transcript variant X7 XM_011540011.2:c.396= XM_011540011.2:c.396C>T XM_011540011.2:c.396C>A
ARHGAP22 transcript variant X11 XM_011540011.1:c.396= XM_011540011.1:c.396C>T XM_011540011.1:c.396C>A
ARHGAP22 transcript variant X3 XM_011540003.2:c.861= XM_011540003.2:c.861C>T XM_011540003.2:c.861C>A
ARHGAP22 transcript variant X3 XM_011540003.1:c.861= XM_011540003.1:c.861C>T XM_011540003.1:c.861C>A
ARHGAP22 transcript variant X2 XM_024448099.2:c.861= XM_024448099.2:c.861C>T XM_024448099.2:c.861C>A
ARHGAP22 transcript variant X2 XM_024448099.1:c.861= XM_024448099.1:c.861C>T XM_024448099.1:c.861C>A
ARHGAP22 transcript variant X17 XM_024448100.2:c.813= XM_024448100.2:c.813C>T XM_024448100.2:c.813C>A
ARHGAP22 transcript variant X12 XM_024448100.1:c.813= XM_024448100.1:c.813C>T XM_024448100.1:c.813C>A
ARHGAP22 transcript variant X6 XM_011540005.2:c.573= XM_011540005.2:c.573C>T XM_011540005.2:c.573C>A
ARHGAP22 transcript variant X4 XM_011540005.1:c.573= XM_011540005.1:c.573C>T XM_011540005.1:c.573C>A
ARHGAP22 transcript variant X19 XM_017016476.2:c.795= XM_017016476.2:c.795C>T XM_017016476.2:c.795C>A
ARHGAP22 transcript variant X14 XM_017016476.1:c.795= XM_017016476.1:c.795C>T XM_017016476.1:c.795C>A
ARHGAP22 transcript variant X5 XM_047425587.1:c.810= XM_047425587.1:c.810C>T XM_047425587.1:c.810C>A
ARHGAP22 transcript variant X4 XM_047425586.1:c.813= XM_047425586.1:c.813C>T XM_047425586.1:c.813C>A
ARHGAP22 transcript variant X11 XM_047425590.1:c.459= XM_047425590.1:c.459C>T XM_047425590.1:c.459C>A
ARHGAP22 transcript variant X9 XM_047425588.1:c.555= XM_047425588.1:c.555C>T XM_047425588.1:c.555C>A
ARHGAP22 transcript variant X18 XM_047425593.1:c.813= XM_047425593.1:c.813C>T XM_047425593.1:c.813C>A
ARHGAP22 transcript variant X10 XM_047425589.1:c.525= XM_047425589.1:c.525C>T XM_047425589.1:c.525C>A
ARHGAP22 transcript variant 5 NM_001256027.1:c.468= NM_001256027.1:c.468C>T NM_001256027.1:c.468C>A
ARHGAP22 transcript variant X16 XM_047425592.1:c.861= XM_047425592.1:c.861C>T XM_047425592.1:c.861C>A
ARHGAP22 transcript variant X12 XM_047425591.1:c.459= XM_047425591.1:c.459C>T XM_047425591.1:c.459C>A
ARHGAP22 transcript variant X21 XM_047425594.1:c.809= XM_047425594.1:c.809C>T XM_047425594.1:c.809C>A
rho GTPase-activating protein 22 isoform 3 NP_067049.2:p.Gly265= NP_067049.2:p.Gly265= NP_067049.2:p.Gly265=
rho GTPase-activating protein 22 isoform 2 NP_001242954.1:p.Gly271= NP_001242954.1:p.Gly271= NP_001242954.1:p.Gly271=
rho GTPase-activating protein 22 isoform 2 NP_001334667.1:p.Gly271= NP_001334667.1:p.Gly271= NP_001334667.1:p.Gly271=
rho GTPase-activating protein 22 isoform 1 NP_001242953.1:p.Gly281= NP_001242953.1:p.Gly281= NP_001242953.1:p.Gly281=
rho GTPase-activating protein 22 isoform 7 NP_001334664.1:p.Gly222= NP_001334664.1:p.Gly222= NP_001334664.1:p.Gly222=
rho GTPase-activating protein 22 isoform 4 NP_001242955.1:p.Gly175= NP_001242955.1:p.Gly175= NP_001242955.1:p.Gly175=
rho GTPase-activating protein 22 isoform X12 XP_011538315.1:p.Gly287= XP_011538315.1:p.Gly287= XP_011538315.1:p.Gly287=
rho GTPase-activating protein 22 isoform X17 XP_011538317.1:p.Gly287= XP_011538317.1:p.Gly287= XP_011538317.1:p.Gly287=
rho GTPase-activating protein 22 isoform X6 XP_005270071.1:p.Gly191= XP_005270071.1:p.Gly191= XP_005270071.1:p.Gly191=
rho GTPase-activating protein 22 isoform X1 XP_011538304.1:p.Gly287= XP_011538304.1:p.Gly287= XP_011538304.1:p.Gly287=
rho GTPase-activating protein 22 isoform X5 XP_011538308.1:p.Gly228= XP_011538308.1:p.Gly228= XP_011538308.1:p.Gly228=
rho GTPase-activating protein 22 isoform X11 XP_016871960.1:p.Gly119= XP_016871960.1:p.Gly119= XP_016871960.1:p.Gly119=
rho GTPase-activating protein 22 isoform X10 XP_011538313.1:p.Gly132= XP_011538313.1:p.Gly132= XP_011538313.1:p.Gly132=
rho GTPase-activating protein 22 isoform X1 XP_011538305.1:p.Gly287= XP_011538305.1:p.Gly287= XP_011538305.1:p.Gly287=
rho GTPase-activating protein 22 isoform X1 XP_024303867.1:p.Gly287= XP_024303867.1:p.Gly287= XP_024303867.1:p.Gly287=
rho GTPase-activating protein 22 isoform X14 XP_024303868.1:p.Gly271= XP_024303868.1:p.Gly271= XP_024303868.1:p.Gly271=
rho GTPase-activating protein 22 isoform X4 XP_011538307.1:p.Gly191= XP_011538307.1:p.Gly191= XP_011538307.1:p.Gly191=
rho GTPase-activating protein 22 isoform X16 XP_016871965.1:p.Gly265= XP_016871965.1:p.Gly265= XP_016871965.1:p.Gly265=
rho GTPase-activating protein 22 isoform X3 XP_047281543.1:p.Gly270= XP_047281543.1:p.Gly270= XP_047281543.1:p.Gly270=
rho GTPase-activating protein 22 isoform X2 XP_047281542.1:p.Gly271= XP_047281542.1:p.Gly271= XP_047281542.1:p.Gly271=
rho GTPase-activating protein 22 isoform X9 XP_047281546.1:p.Gly153= XP_047281546.1:p.Gly153= XP_047281546.1:p.Gly153=
rho GTPase-activating protein 22 isoform X7 XP_047281544.1:p.Gly185= XP_047281544.1:p.Gly185= XP_047281544.1:p.Gly185=
rho GTPase-activating protein 22 isoform X15 XP_047281549.1:p.Gly271= XP_047281549.1:p.Gly271= XP_047281549.1:p.Gly271=
rho GTPase-activating protein 22 isoform X8 XP_047281545.1:p.Gly175= XP_047281545.1:p.Gly175= XP_047281545.1:p.Gly175=
rho GTPase-activating protein 22 isoform X13 XP_047281548.1:p.Gly287= XP_047281548.1:p.Gly287= XP_047281548.1:p.Gly287=
rho GTPase-activating protein 22 isoform X9 XP_047281547.1:p.Gly153= XP_047281547.1:p.Gly153= XP_047281547.1:p.Gly153=
rho GTPase-activating protein 22 isoform X18 XP_047281550.1:p.Ala270= XP_047281550.1:p.Ala270Val XP_047281550.1:p.Ala270Glu
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#.

2 SubSNP, 1 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2738233530 Nov 08, 2017 (151)
2 EVA ss5393255653 Oct 16, 2022 (156)
3 gnomAD - Exomes NC_000010.10 - 49662202 Jul 13, 2019 (153)
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
ss5393255653 NC_000010.10:49662201:G:A NC_000010.11:48454158:G:A
7430104, ss2738233530 NC_000010.10:49662201:G:T NC_000010.11:48454158:G:T (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 rs1482674282

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