SNP Links for Protein (Select 30425400) - SNP

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Links from Protein

Items: 1 to 20 of 235

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Select item 14881185601.

rs1488118560 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:130384802 (GRCh38)
X:129518776 (GRCh37)
Canonical SPDI:: NC_000023.11:130384801:G:A
Gene:: GPR119 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00001/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.130384802G>A, NC_000023.10:g.129518776G>A, NG_016404.1:g.5736C>T, NM_178471.2:c.646C>T, NM_178471.3:c.646C>T, NP_848566.1:p.Arg216Trp

Select item 14789473402.

rs1478947340 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:130384558 (GRCh38)
X:129518532 (GRCh37)
Canonical SPDI:: NC_000023.11:130384557:A:C
Gene:: GPR119 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130384558A>C, NC_000023.10:g.129518532A>C, NG_016404.1:g.5980T>G, NM_178471.2:c.890T>G, NM_178471.3:c.890T>G, NP_848566.1:p.Val297Gly

Select item 14742296913.

rs1474229691 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:130384912 (GRCh38)
X:129518886 (GRCh37)
Canonical SPDI:: NC_000023.11:130384911:A:G
Gene:: GPR119 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.130384912A>G, NC_000023.10:g.129518886A>G, NG_016404.1:g.5626T>C, NM_178471.2:c.536T>C, NM_178471.3:c.536T>C, NP_848566.1:p.Leu179Pro

Select item 14673026674.

rs1467302667 [Homo sapiens]

Variant type:: INS
Alleles:: ->CT [Show Flanks]
Chromosome:: X:130384829 (GRCh38)
X:129518804 (GRCh37)
Canonical SPDI:: NC_000023.11:130384829::CT
Gene:: GPR119 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: CT=0.00001/1 (GnomAD)
CT=0.000011/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130384829_130384830insCT, NC_000023.10:g.129518803_129518804insCT, NG_016404.1:g.5708_5709insAG, NM_178471.2:c.618_619insAG, NM_178471.3:c.618_619insAG, NP_848566.1:p.Ala207fs

Select item 14645342425.

rs1464534242 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:130385366 (GRCh38)
X:129519340 (GRCh37)
Canonical SPDI:: NC_000023.11:130385365:C:T
Gene:: GPR119 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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.130385366C>T, NC_000023.10:g.129519340C>T, NG_016404.1:g.5172G>A, NM_178471.2:c.82G>A, NM_178471.3:c.82G>A, NP_848566.1:p.Ala28Thr

Select item 14521845486.

rs1452184548 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:130385152 (GRCh38)
X:129519126 (GRCh37)
Canonical SPDI:: NC_000023.11:130385151:A:G
Gene:: GPR119 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.130385152A>G, NC_000023.10:g.129519126A>G, NG_016404.1:g.5386T>C, NM_178471.2:c.296T>C, NM_178471.3:c.296T>C, NP_848566.1:p.Ile99Thr

Select item 14375737757.

rs1437573775 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:130384551 (GRCh38)
X:129518525 (GRCh37)
Canonical SPDI:: NC_000023.11:130384550:C:G
Gene:: GPR119 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.130384551C>G, NC_000023.10:g.129518525C>G, NG_016404.1:g.5987G>C, NM_178471.2:c.897G>C, NM_178471.3:c.897G>C, NP_848566.1:p.Lys299Asn

Select item 14332278638.

rs1433227863 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: X:130384823 (GRCh38)
X:129518797 (GRCh37)
Canonical SPDI:: NC_000023.11:130384822:CC:C
Gene:: GPR119 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: -=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130384824del, NC_000023.10:g.129518798del, NG_016404.1:g.5715del, NM_178471.2:c.625del, NM_178471.3:c.625del, NP_848566.1:p.Ala209fs

Select item 14324042529.

rs1432404252 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:130384720 (GRCh38)
X:129518694 (GRCh37)
Canonical SPDI:: NC_000023.11:130384719:A:T
Gene:: GPR119 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000111/1 (ALFA)
T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130384720A>T, NC_000023.10:g.129518694A>T, NG_016404.1:g.5818T>A, NM_178471.2:c.728T>A, NM_178471.3:c.728T>A, NP_848566.1:p.Ile243Asn

Select item 142633121910.

rs1426331219 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:130384920 (GRCh38)
X:129518894 (GRCh37)
Canonical SPDI:: NC_000023.11:130384919:T:A
Gene:: GPR119 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000005/1 (GnomAD_exomes)
A=0.000019/2 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000023.11:g.130384920T>A, NC_000023.10:g.129518894T>A, NG_016404.1:g.5618A>T, NM_178471.2:c.528A>T, NM_178471.3:c.528A>T

Select item 141587276111.

rs1415872761 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:130385200 (GRCh38)
X:129519174 (GRCh37)
Canonical SPDI:: NC_000023.11:130385199:G:T
Gene:: GPR119 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000142/2 (ALFA)
T=0.000005/1 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.130385200G>T, NC_000023.10:g.129519174G>T, NG_016404.1:g.5338C>A, NM_178471.2:c.248C>A, NM_178471.3:c.248C>A, NP_848566.1:p.Ala83Glu

Select item 141207640412.

rs1412076404 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:130384997 (GRCh38)
X:129518971 (GRCh37)
Canonical SPDI:: NC_000023.11:130384996:A:G
Gene:: GPR119 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.130384997A>G, NC_000023.10:g.129518971A>G, NG_016404.1:g.5541T>C, NM_178471.2:c.451T>C, NM_178471.3:c.451T>C, NP_848566.1:p.Tyr151His

Select item 138318623613.

rs1383186236 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:130384584 (GRCh38)
X:129518558 (GRCh37)
Canonical SPDI:: NC_000023.11:130384583:C:T
Gene:: GPR119 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130384584C>T, NC_000023.10:g.129518558C>T, NG_016404.1:g.5954G>A, NM_178471.2:c.864G>A, NM_178471.3:c.864G>A

Select item 138249053614.

rs1382490536 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:130384820 (GRCh38)
X:129518794 (GRCh37)
Canonical SPDI:: NC_000023.11:130384819:C:A,NC_000023.11:130384819:C:T
Gene:: GPR119 (Varview)
Functional Consequence:: missense_variant,stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130384820C>A, NC_000023.11:g.130384820C>T, NC_000023.10:g.129518794C>A, NC_000023.10:g.129518794C>T, NG_016404.1:g.5718G>T, NG_016404.1:g.5718G>A, NM_178471.2:c.628G>T, NM_178471.2:c.628G>A, NM_178471.3:c.628G>T, NM_178471.3:c.628G>A, NP_848566.1:p.Gly210Ter, NP_848566.1:p.Gly210Arg

Select item 137822398815.

rs1378223988 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:130384543 (GRCh38)
X:129518517 (GRCh37)
Canonical SPDI:: NC_000023.11:130384542:G:T
Gene:: GPR119 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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.130384543G>T, NC_000023.10:g.129518517G>T, NG_016404.1:g.5995C>A, NM_178471.2:c.905C>A, NM_178471.3:c.905C>A, NP_848566.1:p.Thr302Asn

Select item 137781619116.

rs1377816191 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:130385136 (GRCh38)
X:129519110 (GRCh37)
Canonical SPDI:: NC_000023.11:130385135:G:A
Gene:: GPR119 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.130385136G>A, NC_000023.10:g.129519110G>A, NG_016404.1:g.5402C>T, NM_178471.2:c.312C>T, NM_178471.3:c.312C>T

Select item 137564201217.

rs1375642012 [Homo sapiens]

Variant type:: INS
Alleles:: ->TT,TTCC [Show Flanks]
Chromosome:: X:130384828 (GRCh38)
X:129518803 (GRCh37)
Canonical SPDI:: NC_000023.11:130384828::TT,NC_000023.11:130384828::TTCC
Gene:: GPR119 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTCC=0./0 (ALFA)
TT=0.000005/1 (GnomAD_exomes)
TT=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.130384828_130384829insTT, NC_000023.11:g.130384828_130384829insTTCC, NC_000023.10:g.129518802_129518803insTT, NC_000023.10:g.129518802_129518803insTTCC, NG_016404.1:g.5709_5710insAA, NG_016404.1:g.5709_5710insGGAA, NM_178471.2:c.619_620insAA, NM_178471.2:c.619_620insGGAA, NM_178471.3:c.619_620insAA, NM_178471.3:c.619_620insGGAA, NP_848566.1:p.Ala207fs, NP_848566.1:p.Ala207fs

Select item 137386432618.

rs1373864326 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:130385354 (GRCh38)
X:129519328 (GRCh37)
Canonical SPDI:: NC_000023.11:130385353:A:G
Gene:: GPR119 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130385354A>G, NC_000023.10:g.129519328A>G, NG_016404.1:g.5184T>C, NM_178471.2:c.94T>C, NM_178471.3:c.94T>C

Select item 137194830019.

rs1371948300 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: X:130384944 (GRCh38)
X:129518918 (GRCh37)
Canonical SPDI:: NC_000023.11:130384943:G:A,NC_000023.11:130384943:G:C
Gene:: GPR119 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
A=0.000005/1 (GnomAD_exomes)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.130384944G>A, NC_000023.11:g.130384944G>C, NC_000023.10:g.129518918G>A, NC_000023.10:g.129518918G>C, NG_016404.1:g.5594C>T, NG_016404.1:g.5594C>G, NM_178471.2:c.504C>T, NM_178471.2:c.504C>G, NM_178471.3:c.504C>T, NM_178471.3:c.504C>G

Select item 136946647120.

rs1369466471 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:130384989 (GRCh38)
X:129518963 (GRCh37)
Canonical SPDI:: NC_000023.11:130384988:C:G
Gene:: GPR119 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000005/1 (GnomAD_exomes)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.130384989C>G, NC_000023.10:g.129518963C>G, NG_016404.1:g.5549G>C, NM_178471.2:c.459G>C, NM_178471.3:c.459G>C

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