SNP Links for Protein (Select 530421724) - SNP

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Links from Protein

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Select item 14845499271.

rs1484549927 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:71616985 (GRCh38)
X:70836835 (GRCh37)
Canonical SPDI:: NC_000023.11:71616984:C:T
Gene:: CXCR3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.71616985C>T, NC_000023.10:g.70836835C>T, NG_029076.1:g.6533G>A, NM_001142797.2:c.628G>A, NM_001142797.1:c.628G>A, NM_001504.2:c.487G>A, NM_001504.1:c.487G>A, XM_005262256.4:c.517G>A, XM_005262256.3:c.517G>A, XM_005262256.2:c.517G>A, XM_005262256.1:c.517G>A, XM_005262257.4:c.517G>A, XM_005262257.3:c.517G>A, XM_005262257.2:c.517G>A, XM_005262257.1:c.517G>A, XM_017029435.2:c.628G>A, XM_017029435.1:c.628G>A, XM_017029436.2:c.487G>A, XM_017029436.1:c.487G>A, XM_047442010.1:c.628G>A, NP_001136269.1:p.Gly210Arg, NP_001495.1:p.Gly163Arg, XP_005262313.1:p.Gly173Arg, XP_005262314.1:p.Gly173Arg, XP_016884924.1:p.Gly210Arg, XP_016884925.1:p.Gly163Arg, XP_047297966.1:p.Gly210Arg

Select item 14828832232.

rs1482883223 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:71617391 (GRCh38)
X:70837241 (GRCh37)
Canonical SPDI:: NC_000023.11:71617390:A:G
Gene:: CXCR3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.71617391A>G, NC_000023.10:g.70837241A>G, NG_029076.1:g.6127T>C, NM_001142797.2:c.222T>C, NM_001142797.1:c.222T>C, NM_001504.2:c.81T>C, NM_001504.1:c.81T>C, XM_005262256.4:c.111T>C, XM_005262256.3:c.111T>C, XM_005262256.2:c.111T>C, XM_005262256.1:c.111T>C, XM_005262257.4:c.111T>C, XM_005262257.3:c.111T>C, XM_005262257.2:c.111T>C, XM_005262257.1:c.111T>C, XM_017029435.2:c.222T>C, XM_017029435.1:c.222T>C, XM_017029436.2:c.81T>C, XM_017029436.1:c.81T>C, XM_047442010.1:c.222T>C

Select item 14825007233.

rs1482500723 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:71616873 (GRCh38)
X:70836723 (GRCh37)
Canonical SPDI:: NC_000023.11:71616872:G:T
Gene:: CXCR3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.71616873G>T, NC_000023.10:g.70836723G>T, NG_029076.1:g.6645C>A, NM_001142797.2:c.740C>A, NM_001142797.1:c.740C>A, NM_001504.2:c.599C>A, NM_001504.1:c.599C>A, XM_005262256.4:c.629C>A, XM_005262256.3:c.629C>A, XM_005262256.2:c.629C>A, XM_005262256.1:c.629C>A, XM_005262257.4:c.629C>A, XM_005262257.3:c.629C>A, XM_005262257.2:c.629C>A, XM_005262257.1:c.629C>A, XM_017029435.2:c.740C>A, XM_017029435.1:c.740C>A, XM_017029436.2:c.599C>A, XM_017029436.1:c.599C>A, XM_047442010.1:c.740C>A, NP_001136269.1:p.Ala247Asp, NP_001495.1:p.Ala200Asp, XP_005262313.1:p.Ala210Asp, XP_005262314.1:p.Ala210Asp, XP_016884924.1:p.Ala247Asp, XP_016884925.1:p.Ala200Asp, XP_047297966.1:p.Ala247Asp

Select item 14824438974.

rs1482443897 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:71617019 (GRCh38)
X:70836869 (GRCh37)
Canonical SPDI:: NC_000023.11:71617018:C:T
Gene:: CXCR3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.71617019C>T, NC_000023.10:g.70836869C>T, NG_029076.1:g.6499G>A, NM_001142797.2:c.594G>A, NM_001142797.1:c.594G>A, NM_001504.2:c.453G>A, NM_001504.1:c.453G>A, XM_005262256.4:c.483G>A, XM_005262256.3:c.483G>A, XM_005262256.2:c.483G>A, XM_005262256.1:c.483G>A, XM_005262257.4:c.483G>A, XM_005262257.3:c.483G>A, XM_005262257.2:c.483G>A, XM_005262257.1:c.483G>A, XM_017029435.2:c.594G>A, XM_017029435.1:c.594G>A, XM_017029436.2:c.453G>A, XM_017029436.1:c.453G>A, XM_047442010.1:c.594G>A

Select item 14795710785.

rs1479571078 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:71618341 (GRCh38)
X:70838191 (GRCh37)
Canonical SPDI:: NC_000023.11:71618340:G:A
Gene:: CXCR3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.71618341G>A, NC_000023.10:g.70838191G>A, NG_029076.1:g.5177C>T, XM_005262256.4:c.32C>T, XM_005262256.3:c.32C>T, XM_005262256.2:c.32C>T, XM_005262256.1:c.32C>T, XM_005262257.4:c.32C>T, XM_005262257.3:c.32C>T, XM_005262257.2:c.32C>T, XM_005262257.1:c.32C>T, XM_017029435.2:c.-102C>T, XM_017029435.1:c.-102C>T, XP_005262313.1:p.Pro11Leu, XP_005262314.1:p.Pro11Leu

Select item 14716209206.

rs1471620920 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:71617420 (GRCh38)
X:70837270 (GRCh37)
Canonical SPDI:: NC_000023.11:71617419:C:T
Gene:: CXCR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000017/3 (GnomAD_exomes)
T=0.000019/2 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000023.11:g.71617420C>T, NC_000023.10:g.70837270C>T, NG_029076.1:g.6098G>A, NM_001142797.2:c.193G>A, NM_001142797.1:c.193G>A, NM_001504.2:c.52G>A, NM_001504.1:c.52G>A, XM_005262256.4:c.82G>A, XM_005262256.3:c.82G>A, XM_005262256.2:c.82G>A, XM_005262256.1:c.82G>A, XM_005262257.4:c.82G>A, XM_005262257.3:c.82G>A, XM_005262257.2:c.82G>A, XM_005262257.1:c.82G>A, XM_017029435.2:c.193G>A, XM_017029435.1:c.193G>A, XM_017029436.2:c.52G>A, XM_017029436.1:c.52G>A, XM_047442010.1:c.193G>A, NP_001136269.1:p.Ala65Thr, NP_001495.1:p.Ala18Thr, XP_005262313.1:p.Ala28Thr, XP_005262314.1:p.Ala28Thr, XP_016884924.1:p.Ala65Thr, XP_016884925.1:p.Ala18Thr, XP_047297966.1:p.Ala65Thr

Select item 14705873257.

rs1470587325 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:71617300 (GRCh38)
X:70837150 (GRCh37)
Canonical SPDI:: NC_000023.11:71617299:C:T
Gene:: CXCR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.71617300C>T, NC_000023.10:g.70837150C>T, NG_029076.1:g.6218G>A, NM_001142797.2:c.313G>A, NM_001142797.1:c.313G>A, NM_001504.2:c.172G>A, NM_001504.1:c.172G>A, XM_005262256.4:c.202G>A, XM_005262256.3:c.202G>A, XM_005262256.2:c.202G>A, XM_005262256.1:c.202G>A, XM_005262257.4:c.202G>A, XM_005262257.3:c.202G>A, XM_005262257.2:c.202G>A, XM_005262257.1:c.202G>A, XM_017029435.2:c.313G>A, XM_017029435.1:c.313G>A, XM_017029436.2:c.172G>A, XM_017029436.1:c.172G>A, XM_047442010.1:c.313G>A, NP_001136269.1:p.Ala105Thr, NP_001495.1:p.Ala58Thr, XP_005262313.1:p.Ala68Thr, XP_005262314.1:p.Ala68Thr, XP_016884924.1:p.Ala105Thr, XP_016884925.1:p.Ala58Thr, XP_047297966.1:p.Ala105Thr

Select item 14685206988.

rs1468520698 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:71616404 (GRCh38)
X:70836254 (GRCh37)
Canonical SPDI:: NC_000023.11:71616403:G:C
Gene:: CXCR3 (Varview)
Functional Consequence:: synonymous_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.71616404G>C, NC_000023.10:g.70836254G>C, NG_029076.1:g.7114C>G, NM_001142797.2:c.1209C>G, NM_001142797.1:c.1209C>G, NM_001504.2:c.1068C>G, NM_001504.1:c.1068C>G, XM_005262256.4:c.1098C>G, XM_005262256.3:c.1098C>G, XM_005262256.2:c.1098C>G, XM_005262256.1:c.1098C>G, XM_005262257.4:c.761C>G, XM_005262257.3:c.761C>G, XM_005262257.2:c.761C>G, XM_005262257.1:c.761C>G, XM_017029435.2:c.1209C>G, XM_017029435.1:c.1209C>G, XM_017029436.2:c.731C>G, XM_017029436.1:c.731C>G, XM_047442010.1:c.872C>G, XP_005262314.1:p.Pro254Arg, XP_016884925.1:p.Pro244Arg, XP_047297966.1:p.Pro291Arg

Select item 14673412679.

rs1467341267 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:71617071 (GRCh38)
X:70836921 (GRCh37)
Canonical SPDI:: NC_000023.11:71617070:T:C
Gene:: CXCR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.71617071T>C, NC_000023.10:g.70836921T>C, NG_029076.1:g.6447A>G, NM_001142797.2:c.542A>G, NM_001142797.1:c.542A>G, NM_001504.2:c.401A>G, NM_001504.1:c.401A>G, XM_005262256.4:c.431A>G, XM_005262256.3:c.431A>G, XM_005262256.2:c.431A>G, XM_005262256.1:c.431A>G, XM_005262257.4:c.431A>G, XM_005262257.3:c.431A>G, XM_005262257.2:c.431A>G, XM_005262257.1:c.431A>G, XM_017029435.2:c.542A>G, XM_017029435.1:c.542A>G, XM_017029436.2:c.401A>G, XM_017029436.1:c.401A>G, XM_047442010.1:c.542A>G, NP_001136269.1:p.Asn181Ser, NP_001495.1:p.Asn134Ser, XP_005262313.1:p.Asn144Ser, XP_005262314.1:p.Asn144Ser, XP_016884924.1:p.Asn181Ser, XP_016884925.1:p.Asn134Ser, XP_047297966.1:p.Asn181Ser

Select item 144915055910.

rs1449150559 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:71616351 (GRCh38)
X:70836201 (GRCh37)
Canonical SPDI:: NC_000023.11:71616350:C:A
Gene:: CXCR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00001/1 (GnomAD)
A=0.000011/3 (TOPMED)
A=0.000084/11 (GnomAD_exomes)
HGVS:: NC_000023.11:g.71616351C>A, NC_000023.10:g.70836201C>A, NG_029076.1:g.7167G>T, NM_001142797.2:c.*14G>T, NM_001142797.1:c.*14G>T, NM_001504.2:c.*14G>T, NM_001504.1:c.*14G>T, XM_005262256.4:c.*14G>T, XM_005262256.3:c.*14G>T, XM_005262256.2:c.*14G>T, XM_005262256.1:c.*14G>T, XM_005262257.4:c.814G>T, XM_005262257.3:c.814G>T, XM_005262257.2:c.814G>T, XM_005262257.1:c.814G>T, XM_017029435.2:c.*14G>T, XM_017029435.1:c.*14G>T, XM_017029436.2:c.784G>T, XM_017029436.1:c.784G>T, XM_047442010.1:c.925G>T, XP_005262314.1:p.Ala272Ser, XP_016884925.1:p.Ala262Ser, XP_047297966.1:p.Ala309Ser

Select item 144796721511.

rs1447967215 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:71616929 (GRCh38)
X:70836779 (GRCh37)
Canonical SPDI:: NC_000023.11:71616928:A:T
Gene:: CXCR3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000006/1 (GnomAD_exomes)
T=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.71616929A>T, NC_000023.10:g.70836779A>T, NG_029076.1:g.6589T>A, NM_001142797.2:c.684T>A, NM_001142797.1:c.684T>A, NM_001504.2:c.543T>A, NM_001504.1:c.543T>A, XM_005262256.4:c.573T>A, XM_005262256.3:c.573T>A, XM_005262256.2:c.573T>A, XM_005262256.1:c.573T>A, XM_005262257.4:c.573T>A, XM_005262257.3:c.573T>A, XM_005262257.2:c.573T>A, XM_005262257.1:c.573T>A, XM_017029435.2:c.684T>A, XM_017029435.1:c.684T>A, XM_017029436.2:c.543T>A, XM_017029436.1:c.543T>A, XM_047442010.1:c.684T>A

Select item 144687911512.

rs1446879115 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:71617385 (GRCh38)
X:70837235 (GRCh37)
Canonical SPDI:: NC_000023.11:71617384:A:G
Gene:: CXCR3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000023.11:g.71617385A>G, NC_000023.10:g.70837235A>G, NG_029076.1:g.6133T>C, NM_001142797.2:c.228T>C, NM_001142797.1:c.228T>C, NM_001504.2:c.87T>C, NM_001504.1:c.87T>C, XM_005262256.4:c.117T>C, XM_005262256.3:c.117T>C, XM_005262256.2:c.117T>C, XM_005262256.1:c.117T>C, XM_005262257.4:c.117T>C, XM_005262257.3:c.117T>C, XM_005262257.2:c.117T>C, XM_005262257.1:c.117T>C, XM_017029435.2:c.228T>C, XM_017029435.1:c.228T>C, XM_017029436.2:c.87T>C, XM_017029436.1:c.87T>C, XM_047442010.1:c.228T>C

Select item 143860294413.

rs1438602944 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:71616414 (GRCh38)
X:70836264 (GRCh37)
Canonical SPDI:: NC_000023.11:71616413:C:T
Gene:: CXCR3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.71616414C>T, NC_000023.10:g.70836264C>T, NG_029076.1:g.7104G>A, NM_001142797.2:c.1199G>A, NM_001142797.1:c.1199G>A, NM_001504.2:c.1058G>A, NM_001504.1:c.1058G>A, XM_005262256.4:c.1088G>A, XM_005262256.3:c.1088G>A, XM_005262256.2:c.1088G>A, XM_005262256.1:c.1088G>A, XM_005262257.4:c.751G>A, XM_005262257.3:c.751G>A, XM_005262257.2:c.751G>A, XM_005262257.1:c.751G>A, XM_017029435.2:c.1199G>A, XM_017029435.1:c.1199G>A, XM_017029436.2:c.721G>A, XM_017029436.1:c.721G>A, XM_047442010.1:c.862G>A, NP_001136269.1:p.Arg400Gln, NP_001495.1:p.Arg353Gln, XP_005262313.1:p.Arg363Gln, XP_005262314.1:p.Gly251Arg, XP_016884924.1:p.Arg400Gln, XP_016884925.1:p.Gly241Arg, XP_047297966.1:p.Gly288Arg

Select item 143342189814.

rs1433421898 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:71617220 (GRCh38)
X:70837070 (GRCh37)
Canonical SPDI:: NC_000023.11:71617219:G:C
Gene:: CXCR3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000051/1 (ALFA)
C=0.000006/1 (GnomAD_exomes)
C=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.71617220G>C, NC_000023.10:g.70837070G>C, NG_029076.1:g.6298C>G, NM_001142797.2:c.393C>G, NM_001142797.1:c.393C>G, NM_001504.2:c.252C>G, NM_001504.1:c.252C>G, XM_005262256.4:c.282C>G, XM_005262256.3:c.282C>G, XM_005262256.2:c.282C>G, XM_005262256.1:c.282C>G, XM_005262257.4:c.282C>G, XM_005262257.3:c.282C>G, XM_005262257.2:c.282C>G, XM_005262257.1:c.282C>G, XM_017029435.2:c.393C>G, XM_017029435.1:c.393C>G, XM_017029436.2:c.252C>G, XM_017029436.1:c.252C>G, XM_047442010.1:c.393C>G

Select item 143327333515.

rs1433273335 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:71617318 (GRCh38)
X:70837168 (GRCh37)
Canonical SPDI:: NC_000023.11:71617317:C:T
Gene:: CXCR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.71617318C>T, NC_000023.10:g.70837168C>T, NG_029076.1:g.6200G>A, NM_001142797.2:c.295G>A, NM_001142797.1:c.295G>A, NM_001504.2:c.154G>A, NM_001504.1:c.154G>A, XM_005262256.4:c.184G>A, XM_005262256.3:c.184G>A, XM_005262256.2:c.184G>A, XM_005262256.1:c.184G>A, XM_005262257.4:c.184G>A, XM_005262257.3:c.184G>A, XM_005262257.2:c.184G>A, XM_005262257.1:c.184G>A, XM_017029435.2:c.295G>A, XM_017029435.1:c.295G>A, XM_017029436.2:c.154G>A, XM_017029436.1:c.154G>A, XM_047442010.1:c.295G>A, NP_001136269.1:p.Asp99Asn, NP_001495.1:p.Asp52Asn, XP_005262313.1:p.Asp62Asn, XP_005262314.1:p.Asp62Asn, XP_016884924.1:p.Asp99Asn, XP_016884925.1:p.Asp52Asn, XP_047297966.1:p.Asp99Asn

Select item 142535635016.

rs1425356350 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:71618334 (GRCh38)
X:70838184 (GRCh37)
Canonical SPDI:: NC_000023.11:71618333:A:T
Gene:: CXCR3 (Varview)
Functional Consequence:: synonymous_variant,intron_variant,coding_sequence_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.71618334A>T, NC_000023.10:g.70838184A>T, NG_029076.1:g.5184T>A, XM_005262256.4:c.39T>A, XM_005262256.3:c.39T>A, XM_005262256.2:c.39T>A, XM_005262256.1:c.39T>A, XM_005262257.4:c.39T>A, XM_005262257.3:c.39T>A, XM_005262257.2:c.39T>A, XM_005262257.1:c.39T>A, XM_017029435.2:c.-95T>A, XM_017029435.1:c.-95T>A

Select item 142008093617.

rs1420080936 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:71617405 (GRCh38)
X:70837255 (GRCh37)
Canonical SPDI:: NC_000023.11:71617404:A:C
Gene:: CXCR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.71617405A>C, NC_000023.10:g.70837255A>C, NG_029076.1:g.6113T>G, NM_001142797.2:c.208T>G, NM_001142797.1:c.208T>G, NM_001504.2:c.67T>G, NM_001504.1:c.67T>G, XM_005262256.4:c.97T>G, XM_005262256.3:c.97T>G, XM_005262256.2:c.97T>G, XM_005262256.1:c.97T>G, XM_005262257.4:c.97T>G, XM_005262257.3:c.97T>G, XM_005262257.2:c.97T>G, XM_005262257.1:c.97T>G, XM_017029435.2:c.208T>G, XM_017029435.1:c.208T>G, XM_017029436.2:c.67T>G, XM_017029436.1:c.67T>G, XM_047442010.1:c.208T>G, NP_001136269.1:p.Phe70Val, NP_001495.1:p.Phe23Val, XP_005262313.1:p.Phe33Val, XP_005262314.1:p.Phe33Val, XP_016884924.1:p.Phe70Val, XP_016884925.1:p.Phe23Val, XP_047297966.1:p.Phe70Val

Select item 141943642018.

rs1419436420 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:71616955 (GRCh38)
X:70836805 (GRCh37)
Canonical SPDI:: NC_000023.11:71616954:G:A
Gene:: CXCR3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000026/7 (TOPMED)
A=0.000038/4 (GnomAD)
HGVS:: NC_000023.11:g.71616955G>A, NC_000023.10:g.70836805G>A, NG_029076.1:g.6563C>T, NM_001142797.2:c.658C>T, NM_001142797.1:c.658C>T, NM_001504.2:c.517C>T, NM_001504.1:c.517C>T, XM_005262256.4:c.547C>T, XM_005262256.3:c.547C>T, XM_005262256.2:c.547C>T, XM_005262256.1:c.547C>T, XM_005262257.4:c.547C>T, XM_005262257.3:c.547C>T, XM_005262257.2:c.547C>T, XM_005262257.1:c.547C>T, XM_017029435.2:c.658C>T, XM_017029435.1:c.658C>T, XM_017029436.2:c.517C>T, XM_017029436.1:c.517C>T, XM_047442010.1:c.658C>T

Select item 141696617519.

rs1416966175 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:71617350 (GRCh38)
X:70837200 (GRCh37)
Canonical SPDI:: NC_000023.11:71617349:G:A
Gene:: CXCR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.71617350G>A, NC_000023.10:g.70837200G>A, NG_029076.1:g.6168C>T, NM_001142797.2:c.263C>T, NM_001142797.1:c.263C>T, NM_001504.2:c.122C>T, NM_001504.1:c.122C>T, XM_005262256.4:c.152C>T, XM_005262256.3:c.152C>T, XM_005262256.2:c.152C>T, XM_005262256.1:c.152C>T, XM_005262257.4:c.152C>T, XM_005262257.3:c.152C>T, XM_005262257.2:c.152C>T, XM_005262257.1:c.152C>T, XM_017029435.2:c.263C>T, XM_017029435.1:c.263C>T, XM_017029436.2:c.122C>T, XM_017029436.1:c.122C>T, XM_047442010.1:c.263C>T, NP_001136269.1:p.Pro88Leu, NP_001495.1:p.Pro41Leu, XP_005262313.1:p.Pro51Leu, XP_005262314.1:p.Pro51Leu, XP_016884924.1:p.Pro88Leu, XP_016884925.1:p.Pro41Leu, XP_047297966.1:p.Pro88Leu

Select item 141540998220.

rs1415409982 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:71616417 (GRCh38)
X:70836267 (GRCh37)
Canonical SPDI:: NC_000023.11:71616416:C:T
Gene:: CXCR3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000026/7 (TOPMED)
T=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.71616417C>T, NC_000023.10:g.70836267C>T, NG_029076.1:g.7101G>A, NM_001142797.2:c.1196G>A, NM_001142797.1:c.1196G>A, NM_001504.2:c.1055G>A, NM_001504.1:c.1055G>A, XM_005262256.4:c.1085G>A, XM_005262256.3:c.1085G>A, XM_005262256.2:c.1085G>A, XM_005262256.1:c.1085G>A, XM_005262257.4:c.748G>A, XM_005262257.3:c.748G>A, XM_005262257.2:c.748G>A, XM_005262257.1:c.748G>A, XM_017029435.2:c.1196G>A, XM_017029435.1:c.1196G>A, XM_017029436.2:c.718G>A, XM_017029436.1:c.718G>A, XM_047442010.1:c.859G>A, NP_001136269.1:p.Arg399His, NP_001495.1:p.Arg352His, XP_005262313.1:p.Arg362His, XP_005262314.1:p.Ala250Thr, XP_016884924.1:p.Arg399His, XP_016884925.1:p.Ala240Thr, XP_047297966.1:p.Ala287Thr

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