SNP Links for Protein (Select 52317162) - SNP

Links from Protein

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Select item 14908485321.

rs1490848532 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:15088090 (GRCh38)
19:15198901 (GRCh37)
Canonical SPDI:: NC_000019.10:15088089:C:A
Gene:: OR1I1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.15088090C>A, NC_000019.9:g.15198901C>A, NM_001004713.2:c.1025C>A, NM_001004713.1:c.1025C>A, NP_001004713.1:p.Pro342His

Select item 14880971562.

rs1488097156 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:15088088 (GRCh38)
19:15198899 (GRCh37)
Canonical SPDI:: NC_000019.10:15088087:C:G
Gene:: OR1I1 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.15088088C>G, NC_000019.9:g.15198899C>G, NM_001004713.2:c.1023C>G, NM_001004713.1:c.1023C>G, NP_001004713.1:p.Tyr341Ter

Select item 14828287583.

rs1482828758 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 19:15087133 (GRCh38)
19:15197944 (GRCh37)
Canonical SPDI:: NC_000019.10:15087132:A:C
Gene:: OR1I1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15087133A>C, NC_000019.9:g.15197944A>C, NM_001004713.2:c.68A>C, NM_001004713.1:c.68A>C, NP_001004713.1:p.His23Pro

Select item 14787603494.

rs1478760349 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:15087491 (GRCh38)
19:15198302 (GRCh37)
Canonical SPDI:: NC_000019.10:15087490:G:A
Gene:: OR1I1 (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=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.15087491G>A, NC_000019.9:g.15198302G>A, NM_001004713.2:c.426G>A, NM_001004713.1:c.426G>A

Select item 14779667685.

rs1477966768 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:15087511 (GRCh38)
19:15198322 (GRCh37)
Canonical SPDI:: NC_000019.10:15087510:G:A
Gene:: OR1I1 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15087511G>A, NC_000019.9:g.15198322G>A, NM_001004713.2:c.446G>A, NM_001004713.1:c.446G>A, NP_001004713.1:p.Trp149Ter

Select item 14772192586.

rs1477219258 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:15087776 (GRCh38)
19:15198587 (GRCh37)
Canonical SPDI:: NC_000019.10:15087775:C:T
Gene:: OR1I1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.15087776C>T, NC_000019.9:g.15198587C>T, NM_001004713.2:c.711C>T, NM_001004713.1:c.711C>T

Select item 14758583397.

rs1475858339 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 19:15087943 (GRCh38)
19:15198754 (GRCh37)
Canonical SPDI:: NC_000019.10:15087942:G:A,NC_000019.10:15087942:G:T
Gene:: OR1I1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000066/1 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000029/4 (GnomAD)
A=0.000035/1 (TOMMO)
A=0.000223/1 (Estonian)
HGVS:: NC_000019.10:g.15087943G>A, NC_000019.10:g.15087943G>T, NC_000019.9:g.15198754G>A, NC_000019.9:g.15198754G>T, NM_001004713.2:c.878G>A, NM_001004713.2:c.878G>T, NM_001004713.1:c.878G>A, NM_001004713.1:c.878G>T, NP_001004713.1:p.Arg293Gln, NP_001004713.1:p.Arg293Leu

Select item 14746873348.

rs1474687334 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:15087912 (GRCh38)
19:15198723 (GRCh37)
Canonical SPDI:: NC_000019.10:15087911:C:T
Gene:: OR1I1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15087912C>T, NC_000019.9:g.15198723C>T, NM_001004713.2:c.847C>T, NM_001004713.1:c.847C>T, NP_001004713.1:p.Pro283Ser

Select item 14714117029.

rs1471411702 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:15087371 (GRCh38)
19:15198182 (GRCh37)
Canonical SPDI:: NC_000019.10:15087370:T:G
Gene:: OR1I1 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15087371T>G, NC_000019.9:g.15198182T>G, NM_001004713.2:c.306T>G, NM_001004713.1:c.306T>G, NP_001004713.1:p.Tyr102Ter

Select item 146626876010.

rs1466268760 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:15087372 (GRCh38)
19:15198183 (GRCh37)
Canonical SPDI:: NC_000019.10:15087371:G:A
Gene:: OR1I1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000019.10:g.15087372G>A, NC_000019.9:g.15198183G>A, NM_001004713.2:c.307G>A, NM_001004713.1:c.307G>A, NP_001004713.1:p.Ala103Thr

Select item 146464274711.

rs1464642747 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:15087070 (GRCh38)
19:15197881 (GRCh37)
Canonical SPDI:: NC_000019.10:15087069:A:G
Gene:: OR1I1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.15087070A>G, NC_000019.9:g.15197881A>G, NM_001004713.2:c.5A>G, NM_001004713.1:c.5A>G, NP_001004713.1:p.Glu2Gly

Select item 145844261212.

rs1458442612 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 19:15087160 (GRCh38)
19:15197971 (GRCh37)
Canonical SPDI:: NC_000019.10:15087159:T:C,NC_000019.10:15087159:T:G
Gene:: OR1I1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000019.10:g.15087160T>C, NC_000019.10:g.15087160T>G, NC_000019.9:g.15197971T>C, NC_000019.9:g.15197971T>G, NM_001004713.2:c.95T>C, NM_001004713.2:c.95T>G, NM_001004713.1:c.95T>C, NM_001004713.1:c.95T>G, NP_001004713.1:p.Leu32Pro, NP_001004713.1:p.Leu32Arg

Select item 145811590413.

rs1458115904 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:15087775 (GRCh38)
19:15198586 (GRCh37)
Canonical SPDI:: NC_000019.10:15087774:C:A
Gene:: OR1I1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.15087775C>A, NC_000019.9:g.15198586C>A, NM_001004713.2:c.710C>A, NM_001004713.1:c.710C>A, NP_001004713.1:p.Ala237Asp

Select item 145801783614.

rs1458017836 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:15087979 (GRCh38)
19:15198790 (GRCh37)
Canonical SPDI:: NC_000019.10:15087978:T:C
Gene:: OR1I1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.15087979T>C, NC_000019.9:g.15198790T>C, NM_001004713.2:c.914T>C, NM_001004713.1:c.914T>C, NP_001004713.1:p.Ile305Thr

Select item 144775685015.

rs1447756850 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:15087408 (GRCh38)
19:15198219 (GRCh37)
Canonical SPDI:: NC_000019.10:15087407:C:T
Gene:: OR1I1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.15087408C>T, NC_000019.9:g.15198219C>T, NM_001004713.2:c.343C>T, NM_001004713.1:c.343C>T

Select item 143533196116.

rs1435331961 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:15087227 (GRCh38)
19:15198038 (GRCh37)
Canonical SPDI:: NC_000019.10:15087226:C:T
Gene:: OR1I1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15087227C>T, NC_000019.9:g.15198038C>T, NM_001004713.2:c.162C>T, NM_001004713.1:c.162C>T

Select item 143448753117.

rs1434487531 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:15088082 (GRCh38)
19:15198893 (GRCh37)
Canonical SPDI:: NC_000019.10:15088081:C:G
Gene:: OR1I1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/3 (GnomAD_exomes)
G=0.000015/4 (TOPMED)
G=0.000029/4 (GnomAD)
HGVS:: NC_000019.10:g.15088082C>G, NC_000019.9:g.15198893C>G, NM_001004713.2:c.1017C>G, NM_001004713.1:c.1017C>G, NP_001004713.1:p.Ile339Met

Select item 143430975718.

rs1434309757 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGCCCCTGCTGAAGCTCTCCGGCTCA>- [Show Flanks]
Chromosome:: 19:15087610 (GRCh38)
19:15198421 (GRCh37)
Canonical SPDI:: NC_000019.10:15087605:CTCATGCCCCTGCTGAAGCTCTCCGGCTCA:CTCA
Gene:: OR1I1 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.15087610_15087635del, NC_000019.9:g.15198421_15198446del, NM_001004713.2:c.545_570del, NM_001004713.1:c.545_570del, NP_001004713.1:p.Met182fs

Select item 143238718219.

rs1432387182 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:15087290 (GRCh38)
19:15198101 (GRCh37)
Canonical SPDI:: NC_000019.10:15087289:C:T
Gene:: OR1I1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.15087290C>T, NC_000019.9:g.15198101C>T, NM_001004713.2:c.225C>T, NM_001004713.1:c.225C>T

Select item 143232114120.

rs1432321141 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:15087237 (GRCh38)
19:15198048 (GRCh37)
Canonical SPDI:: NC_000019.10:15087236:C:A
Gene:: OR1I1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15087237C>A, NC_000019.9:g.15198048C>A, NM_001004713.2:c.172C>A, NM_001004713.1:c.172C>A, NP_001004713.1:p.Pro58Thr

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