SNP Links for Protein (Select 95091988) - SNP

Links from Protein

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Select item 14902022721.

rs1490202272 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:11254662 (GRCh38)
X:11272782 (GRCh37)
Canonical SPDI:: NC_000023.11:11254661:T:G
Gene:: ARHGAP6 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.11254662T>G, NC_000023.10:g.11272782T>G, NG_012494.2:g.416040A>C, NM_013427.3:c.634A>C, NM_013427.2:c.634A>C, NM_013423.3:c.25A>C, NM_013423.2:c.25A>C, NM_006125.3:c.634A>C, NM_006125.2:c.634A>C, NR_109776.2:n.1822A>C, NR_109776.1:n.1603A>C, NM_001287242.2:c.94A>C, NM_001287242.1:c.94A>C, NM_001174.3:c.730A>C, NM_001174.2:c.100A>C, NM_013422.2:c.730A>C, NM_013422.1:c.25A>C, NM_001174.1:c.100A>C

Select item 14887235302.

rs1488723530 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:11188824 (GRCh38)
X:11206944 (GRCh37)
Canonical SPDI:: NC_000023.11:11188823:G:C
Gene:: ARHGAP6 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.11188824G>C, NC_000023.10:g.11206944G>C, NG_012494.2:g.481878C>G, NM_013427.3:c.981C>G, NM_013427.2:c.981C>G, NM_013423.3:c.372C>G, NM_013423.2:c.372C>G, NM_006125.3:c.981C>G, NM_006125.2:c.981C>G, NR_109776.2:n.2169C>G, NR_109776.1:n.1950C>G, NM_001287242.2:c.441C>G, NM_001287242.1:c.441C>G, NM_001174.3:c.1077C>G, NM_001174.2:c.447C>G, NM_013422.2:c.1077C>G, NM_013422.1:c.372C>G, NM_001174.1:c.447C>G

Select item 14886461613.

rs1488646161 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:11169529 (GRCh38)
X:11187649 (GRCh37)
Canonical SPDI:: NC_000023.11:11169528:A:C
Gene:: ARHGAP6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.11169529A>C, NC_000023.10:g.11187649A>C, NG_012494.2:g.501173T>G, NM_013427.3:c.1785T>G, NM_013427.2:c.1785T>G, NM_013423.3:c.1176T>G, NM_013423.2:c.1176T>G, NM_006125.3:c.1785T>G, NM_006125.2:c.1785T>G, NR_109776.2:n.2973T>G, NR_109776.1:n.2754T>G, NM_001287242.2:c.1245T>G, NM_001287242.1:c.1245T>G, NM_001174.3:c.1881T>G, NM_001174.2:c.1251T>G, NM_013422.2:c.1881T>G, NM_013422.1:c.1176T>G, NM_001174.1:c.1251T>G, NP_038286.2:p.Ile595Met, NP_038267.1:p.Ile392Met, NP_006116.2:p.Ile595Met, NP_001274171.1:p.Ile415Met

Select item 14878958624.

rs1487895862 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: X:11664613 (GRCh38)
X:11682733 (GRCh37)
Canonical SPDI:: NC_000023.11:11664612:G:A,NC_000023.11:11664612:G:T
Gene:: ARHGAP6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
HGVS:: NC_000023.11:g.11664613G>A, NC_000023.11:g.11664613G>T, NC_000023.10:g.11682733G>A, NC_000023.10:g.11682733G>T, NG_012494.2:g.6089C>T, NG_012494.2:g.6089C>A, NM_013427.3:c.216C>T, NM_013427.3:c.216C>A, NM_013427.2:c.216C>T, NM_013427.2:c.216C>A, NM_006125.3:c.216C>T, NM_006125.3:c.216C>A, NM_006125.2:c.216C>T, NM_006125.2:c.216C>A, NR_109776.2:n.1308C>T, NR_109776.2:n.1308C>A, NR_109776.1:n.1089C>T, NR_109776.1:n.1089C>A, NM_001174.3:c.216C>T, NM_001174.3:c.216C>A, NM_001174.2:c.-415C>T, NM_001174.2:c.-415C>A, NM_013422.2:c.216C>T, NM_013422.2:c.216C>A

Select item 14858859295.

rs1485885929 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:11143960 (GRCh38)
X:11162080 (GRCh37)
Canonical SPDI:: NC_000023.11:11143959:G:C
Gene:: ARHGAP6 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.11143960G>C, NC_000023.10:g.11162080G>C, NG_012494.2:g.526742C>G, NM_006125.3:c.2196C>G, NM_006125.2:c.2196C>G, NM_013422.2:c.2292C>G, NM_013422.1:c.1587C>G, NM_001174.1:c.*309C>G, NP_006116.2:p.Ser732Arg

Select item 14845363016.

rs1484536301 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:11143899 (GRCh38)
X:11162019 (GRCh37)
Canonical SPDI:: NC_000023.11:11143898:G:A
Gene:: ARHGAP6 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.11143899G>A, NC_000023.10:g.11162019G>A, NG_012494.2:g.526803C>T, NM_006125.3:c.2257C>T, NM_006125.2:c.2257C>T, NM_013422.2:c.2353C>T, NM_013422.1:c.1648C>T, NM_001174.1:c.*370C>T, NP_006116.2:p.Arg753Trp

Select item 14824721587.

rs1482472158 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:11664793 (GRCh38)
X:11682913 (GRCh37)
Canonical SPDI:: NC_000023.11:11664792:G:A
Gene:: ARHGAP6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
HGVS:: NC_000023.11:g.11664793G>A, NC_000023.10:g.11682913G>A, NG_012494.2:g.5909C>T, NM_013427.3:c.36C>T, NM_013427.2:c.36C>T, NM_006125.3:c.36C>T, NM_006125.2:c.36C>T, NR_109776.2:n.1128C>T, NR_109776.1:n.909C>T, NM_001174.3:c.36C>T, NM_001174.2:c.-595C>T, NM_013422.2:c.36C>T

Select item 14820199498.

rs1482019949 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:11188958 (GRCh38)
X:11207078 (GRCh37)
Canonical SPDI:: NC_000023.11:11188957:G:A
Gene:: ARHGAP6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.11188958G>A, NC_000023.10:g.11207078G>A, NG_012494.2:g.481744C>T, NM_013427.3:c.847C>T, NM_013427.2:c.847C>T, NM_013423.3:c.238C>T, NM_013423.2:c.238C>T, NM_006125.3:c.847C>T, NM_006125.2:c.847C>T, NR_109776.2:n.2035C>T, NR_109776.1:n.1816C>T, NM_001287242.2:c.307C>T, NM_001287242.1:c.307C>T, NM_001174.3:c.943C>T, NM_001174.2:c.313C>T, NM_013422.2:c.943C>T, NM_013422.1:c.238C>T, NM_001174.1:c.313C>T, NP_038286.2:p.Pro283Ser, NP_038267.1:p.Pro80Ser, NP_006116.2:p.Pro283Ser, NP_001274171.1:p.Pro103Ser

Select item 14820080849.

rs1482008084 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:11664549 (GRCh38)
X:11682669 (GRCh37)
Canonical SPDI:: NC_000023.11:11664548:G:A
Gene:: ARHGAP6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
HGVS:: NC_000023.11:g.11664549G>A, NC_000023.10:g.11682669G>A, NG_012494.2:g.6153C>T, NM_013427.3:c.280C>T, NM_013427.2:c.280C>T, NM_006125.3:c.280C>T, NM_006125.2:c.280C>T, NR_109776.2:n.1372C>T, NR_109776.1:n.1153C>T, NM_001174.3:c.280C>T, NM_001174.2:c.-351C>T, NM_013422.2:c.280C>T, NP_038286.2:p.Pro94Ser, NP_006116.2:p.Pro94Ser

Select item 148069619610.

rs1480696196 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:11186408 (GRCh38)
X:11204528 (GRCh37)
Canonical SPDI:: NC_000023.11:11186407:G:T
Gene:: ARHGAP6 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
HGVS:: NC_000023.11:g.11186408G>T, NC_000023.10:g.11204528G>T, NG_012494.2:g.484294C>A, NM_013427.3:c.1101C>A, NM_013427.2:c.1101C>A, NM_013423.3:c.492C>A, NM_013423.2:c.492C>A, NM_006125.3:c.1101C>A, NM_006125.2:c.1101C>A, NR_109776.2:n.2289C>A, NR_109776.1:n.2070C>A, NM_001287242.2:c.561C>A, NM_001287242.1:c.561C>A, NM_001174.3:c.1197C>A, NM_001174.2:c.567C>A, NM_013422.2:c.1197C>A, NM_013422.1:c.492C>A, NM_001174.1:c.567C>A

Select item 148025371911.

rs1480253719 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:11143920 (GRCh38)
X:11162040 (GRCh37)
Canonical SPDI:: NC_000023.11:11143919:C:T
Gene:: ARHGAP6 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000187/2 (ALFA)
T=0.000005/1 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.11143920C>T, NC_000023.10:g.11162040C>T, NG_012494.2:g.526782G>A, NM_006125.3:c.2236G>A, NM_006125.2:c.2236G>A, NM_013422.2:c.2332G>A, NM_013422.1:c.1627G>A, NM_001174.1:c.*349G>A, NP_006116.2:p.Val746Met

Select item 147981672912.

rs1479816729 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:11664555 (GRCh38)
X:11682675 (GRCh37)
Canonical SPDI:: NC_000023.11:11664554:T:G
Gene:: ARHGAP6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
HGVS:: NC_000023.11:g.11664555T>G, NC_000023.10:g.11682675T>G, NG_012494.2:g.6147A>C, NM_013427.3:c.274A>C, NM_013427.2:c.274A>C, NM_006125.3:c.274A>C, NM_006125.2:c.274A>C, NR_109776.2:n.1366A>C, NR_109776.1:n.1147A>C, NM_001174.3:c.274A>C, NM_001174.2:c.-357A>C, NM_013422.2:c.274A>C

Select item 147855516713.

rs1478555167 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:11188731 (GRCh38)
X:11206851 (GRCh37)
Canonical SPDI:: NC_000023.11:11188730:C:T
Gene:: ARHGAP6 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.11188731C>T, NC_000023.10:g.11206851C>T, NG_012494.2:g.481971G>A, NM_013427.3:c.1074G>A, NM_013427.2:c.1074G>A, NM_013423.3:c.465G>A, NM_013423.2:c.465G>A, NM_006125.3:c.1074G>A, NM_006125.2:c.1074G>A, NR_109776.2:n.2262G>A, NR_109776.1:n.2043G>A, NM_001287242.2:c.534G>A, NM_001287242.1:c.534G>A, NM_001174.3:c.1170G>A, NM_001174.2:c.540G>A, NM_013422.2:c.1170G>A, NM_013422.1:c.465G>A, NM_001174.1:c.540G>A

Select item 147767000714.

rs1477670007 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:11178185 (GRCh38)
X:11196305 (GRCh37)
Canonical SPDI:: NC_000023.11:11178184:T:C
Gene:: ARHGAP6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.11178185T>C, NC_000023.10:g.11196305T>C, NG_012494.2:g.492517A>G, NM_013427.3:c.1544A>G, NM_013427.2:c.1544A>G, NM_013423.3:c.935A>G, NM_013423.2:c.935A>G, NM_006125.3:c.1544A>G, NM_006125.2:c.1544A>G, NR_109776.2:n.2732A>G, NR_109776.1:n.2513A>G, NM_001287242.2:c.1004A>G, NM_001287242.1:c.1004A>G, NM_001174.3:c.1640A>G, NM_001174.2:c.1010A>G, NM_013422.2:c.1640A>G, NM_013422.1:c.935A>G, NM_001174.1:c.1010A>G, NP_038286.2:p.Asn515Ser, NP_038267.1:p.Asn312Ser, NP_006116.2:p.Asn515Ser, NP_001274171.1:p.Asn335Ser

Select item 147628926715.

rs1476289267 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:11144133 (GRCh38)
X:11162253 (GRCh37)
Canonical SPDI:: NC_000023.11:11144132:C:T
Gene:: ARHGAP6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00001/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.11144133C>T, NC_000023.10:g.11162253C>T, NG_012494.2:g.526569G>A, NM_013427.3:c.2023G>A, NM_013427.2:c.2023G>A, NM_013423.3:c.1414G>A, NM_013423.2:c.1414G>A, NM_006125.3:c.2023G>A, NM_006125.2:c.2023G>A, NR_109776.2:n.3301G>A, NR_109776.1:n.3082G>A, NM_001287242.2:c.1483G>A, NM_001287242.1:c.1483G>A, NM_001174.3:c.*136G>A, NM_001174.2:c.*136G>A, NM_013422.2:c.2119G>A, NM_013422.1:c.1414G>A, NM_001174.1:c.*136G>A, NP_038286.2:p.Val675Met, NP_038267.1:p.Val472Met, NP_006116.2:p.Val675Met, NP_001274171.1:p.Val495Met

Select item 146214989016.

rs1462149890 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:11144078 (GRCh38)
X:11162198 (GRCh37)
Canonical SPDI:: NC_000023.11:11144077:G:A
Gene:: ARHGAP6 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000019/2 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000023.11:g.11144078G>A, NC_000023.10:g.11162198G>A, NG_012494.2:g.526624C>T, NM_013427.3:c.2078C>T, NM_013427.2:c.2078C>T, NM_013423.3:c.1469C>T, NM_013423.2:c.1469C>T, NM_006125.3:c.2078C>T, NM_006125.2:c.2078C>T, NR_109776.2:n.3356C>T, NR_109776.1:n.3137C>T, NM_001287242.2:c.1538C>T, NM_001287242.1:c.1538C>T, NM_001174.3:c.*191C>T, NM_001174.2:c.*191C>T, NM_013422.2:c.2174C>T, NM_013422.1:c.1469C>T, NM_001174.1:c.*191C>T, NP_038286.2:p.Ser693Leu, NP_038267.1:p.Ser490Leu, NP_006116.2:p.Ser693Leu, NP_001274171.1:p.Ser513Leu

Select item 146134859417.

rs1461348594 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:11144152 (GRCh38)
X:11162272 (GRCh37)
Canonical SPDI:: NC_000023.11:11144151:A:G
Gene:: ARHGAP6 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.11144152A>G, NC_000023.10:g.11162272A>G, NG_012494.2:g.526550T>C, NM_013427.3:c.2004T>C, NM_013427.2:c.2004T>C, NM_013423.3:c.1395T>C, NM_013423.2:c.1395T>C, NM_006125.3:c.2004T>C, NM_006125.2:c.2004T>C, NR_109776.2:n.3282T>C, NR_109776.1:n.3063T>C, NM_001287242.2:c.1464T>C, NM_001287242.1:c.1464T>C, NM_001174.3:c.*117T>C, NM_001174.2:c.*117T>C, NM_013422.2:c.2100T>C, NM_013422.1:c.1395T>C, NM_001174.1:c.*117T>C

Select item 145932647718.

rs1459326477 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:11664600 (GRCh38)
X:11682720 (GRCh37)
Canonical SPDI:: NC_000023.11:11664599:G:A
Gene:: ARHGAP6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.11664600G>A, NC_000023.10:g.11682720G>A, NG_012494.2:g.6102C>T, NM_013427.3:c.229C>T, NM_013427.2:c.229C>T, NM_006125.3:c.229C>T, NM_006125.2:c.229C>T, NR_109776.2:n.1321C>T, NR_109776.1:n.1102C>T, NM_001174.3:c.229C>T, NM_001174.2:c.-402C>T, NM_013422.2:c.229C>T, NP_038286.2:p.Pro77Ser, NP_006116.2:p.Pro77Ser

Select item 145804701219.

rs1458047012 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:11186246 (GRCh38)
X:11204366 (GRCh37)
Canonical SPDI:: NC_000023.11:11186245:T:C
Gene:: ARHGAP6 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.11186246T>C, NC_000023.10:g.11204366T>C, NG_012494.2:g.484456A>G, NM_013427.3:c.1263A>G, NM_013427.2:c.1263A>G, NM_013423.3:c.654A>G, NM_013423.2:c.654A>G, NM_006125.3:c.1263A>G, NM_006125.2:c.1263A>G, NR_109776.2:n.2451A>G, NR_109776.1:n.2232A>G, NM_001287242.2:c.723A>G, NM_001287242.1:c.723A>G, NM_001174.3:c.1359A>G, NM_001174.2:c.729A>G, NM_013422.2:c.1359A>G, NM_013422.1:c.654A>G, NM_001174.1:c.729A>G

Select item 145791450520.

rs1457914505 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:11664819 (GRCh38)
X:11682939 (GRCh37)
Canonical SPDI:: NC_000023.11:11664818:G:T
Gene:: ARHGAP6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.11664819G>T, NC_000023.10:g.11682939G>T, NG_012494.2:g.5883C>A, NM_013427.3:c.10C>A, NM_013427.2:c.10C>A, NM_006125.3:c.10C>A, NM_006125.2:c.10C>A, NR_109776.2:n.1102C>A, NR_109776.1:n.883C>A, NM_001174.3:c.10C>A, NM_001174.2:c.-621C>A, NM_013422.2:c.10C>A, NP_038286.2:p.Gln4Lys, NP_006116.2:p.Gln4Lys

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