SNP Links for Protein (Select 52218830) - SNP

Links from Protein

Items: 1 to 20 of 415

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Select item 14892070881.

rs1489207088 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:124038775 (GRCh38)
11:123909482 (GRCh37)
Canonical SPDI:: NC_000011.10:124038774:A:G
Gene:: OR10G7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.124038775A>G, NC_000011.9:g.123909482A>G, NM_001004463.2:c.227T>C, NM_001004463.1:c.227T>C, NP_001004463.1:p.Val76Ala

Select item 14890303742.

rs1489030374 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:124038581 (GRCh38)
11:123909288 (GRCh37)
Canonical SPDI:: NC_000011.10:124038580:C:A
Gene:: OR10G7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.124038581C>A, NC_000011.9:g.123909288C>A, NM_001004463.2:c.421G>T, NM_001004463.1:c.421G>T, NP_001004463.1:p.Ala141Ser

Select item 14874276203.

rs1487427620 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:124038177 (GRCh38)
11:123908884 (GRCh37)
Canonical SPDI:: NC_000011.10:124038176:G:A
Gene:: OR10G7 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.124038177G>A, NC_000011.9:g.123908884G>A, NM_001004463.2:c.825C>T, NM_001004463.1:c.825C>T

Select item 14847015254.

rs1484701525 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 11:124038522 (GRCh38)
11:123909229 (GRCh37)
Canonical SPDI:: NC_000011.10:124038521:T:C,NC_000011.10:124038521:T:G
Gene:: OR10G7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.124038522T>C, NC_000011.10:g.124038522T>G, NC_000011.9:g.123909229T>C, NC_000011.9:g.123909229T>G, NM_001004463.2:c.480A>G, NM_001004463.2:c.480A>C, NM_001004463.1:c.480A>G, NM_001004463.1:c.480A>C, NP_001004463.1:p.Ile160Met

Select item 14836789135.

rs1483678913 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:124038636 (GRCh38)
11:123909343 (GRCh37)
Canonical SPDI:: NC_000011.10:124038635:G:A
Gene:: OR10G7 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.124038636G>A, NC_000011.9:g.123909343G>A, NM_001004463.2:c.366C>T, NM_001004463.1:c.366C>T

Select item 14802292596.

rs1480229259 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:124038641 (GRCh38)
11:123909348 (GRCh37)
Canonical SPDI:: NC_000011.10:124038640:G:A
Gene:: OR10G7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
A=0.000012/3 (GnomAD_exomes)
A=0.000142/2 (TOMMO)
HGVS:: NC_000011.10:g.124038641G>A, NC_000011.9:g.123909348G>A, NM_001004463.2:c.361C>T, NM_001004463.1:c.361C>T, NP_001004463.1:p.Arg121Cys

Select item 14788263187.

rs1478826318 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:124038228 (GRCh38)
11:123908935 (GRCh37)
Canonical SPDI:: NC_000011.10:124038227:G:A
Gene:: OR10G7 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000011.10:g.124038228G>A, NC_000011.9:g.123908935G>A, NM_001004463.2:c.774C>T, NM_001004463.1:c.774C>T

Select item 14713555108.

rs1471355510 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:124038377 (GRCh38)
11:123909084 (GRCh37)
Canonical SPDI:: NC_000011.10:124038376:A:G
Gene:: OR10G7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.124038377A>G, NC_000011.9:g.123909084A>G, NM_001004463.2:c.625T>C, NM_001004463.1:c.625T>C, NP_001004463.1:p.Cys209Arg

Select item 14694388319.

rs1469438831 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:124038290 (GRCh38)
11:123908997 (GRCh37)
Canonical SPDI:: NC_000011.10:124038289:G:C
Gene:: OR10G7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000011.10:g.124038290G>C, NC_000011.9:g.123908997G>C, NM_001004463.2:c.712C>G, NM_001004463.1:c.712C>G, NP_001004463.1:p.Gln238Glu

Select item 146891137810.

rs1468911378 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:124038833 (GRCh38)
11:123909540 (GRCh37)
Canonical SPDI:: NC_000011.10:124038832:T:G
Gene:: OR10G7 (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=0.000004/1 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.124038833T>G, NC_000011.9:g.123909540T>G, NM_001004463.2:c.169A>C, NM_001004463.1:c.169A>C, NP_001004463.1:p.Met57Leu

Select item 146644281011.

rs1466442810 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:124038186 (GRCh38)
11:123908893 (GRCh37)
Canonical SPDI:: NC_000011.10:124038185:G:A
Gene:: OR10G7 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.124038186G>A, NC_000011.9:g.123908893G>A, NM_001004463.2:c.816C>T, NM_001004463.1:c.816C>T

Select item 146476001612.

rs1464760016 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:124038073 (GRCh38)
11:123908780 (GRCh37)
Canonical SPDI:: NC_000011.10:124038072:C:G,NC_000011.10:124038072:C:T
Gene:: OR10G7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.124038073C>G, NC_000011.10:g.124038073C>T, NC_000011.9:g.123908780C>G, NC_000011.9:g.123908780C>T, NM_001004463.2:c.929G>C, NM_001004463.2:c.929G>A, NM_001004463.1:c.929G>C, NM_001004463.1:c.929G>A, NP_001004463.1:p.Gly310Ala, NP_001004463.1:p.Gly310Asp

Select item 146140329813.

rs1461403298 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:124038274 (GRCh38)
11:123908981 (GRCh37)
Canonical SPDI:: NC_000011.10:124038273:T:C
Gene:: OR10G7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.124038274T>C, NC_000011.9:g.123908981T>C, NM_001004463.2:c.728A>G, NM_001004463.1:c.728A>G, NP_001004463.1:p.His243Arg

Select item 145694096514.

rs1456940965 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:124038692 (GRCh38)
11:123909399 (GRCh37)
Canonical SPDI:: NC_000011.10:124038691:G:A
Gene:: OR10G7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.124038692G>A, NC_000011.9:g.123909399G>A, NM_001004463.2:c.310C>T, NM_001004463.1:c.310C>T, NP_001004463.1:p.His104Tyr

Select item 145357376215.

rs1453573762 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:124038744 (GRCh38)
11:123909451 (GRCh37)
Canonical SPDI:: NC_000011.10:124038743:T:G
Gene:: OR10G7 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.124038744T>G, NC_000011.9:g.123909451T>G, NM_001004463.2:c.258A>C, NM_001004463.1:c.258A>C

Select item 145284425316.

rs1452844253 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:124038656 (GRCh38)
11:123909363 (GRCh37)
Canonical SPDI:: NC_000011.10:124038655:C:T
Gene:: OR10G7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.124038656C>T, NC_000011.9:g.123909363C>T, NM_001004463.2:c.346G>A, NM_001004463.1:c.346G>A, NP_001004463.1:p.Val116Ile

Select item 144962954217.

rs1449629542 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:124038128 (GRCh38)
11:123908835 (GRCh37)
Canonical SPDI:: NC_000011.10:124038127:T:A
Gene:: OR10G7 (Varview)
Functional Consequence:: stop_gained,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_000011.10:g.124038128T>A, NC_000011.9:g.123908835T>A, NM_001004463.2:c.874A>T, NM_001004463.1:c.874A>T, NP_001004463.1:p.Lys292Ter

Select item 144934475718.

rs1449344757 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:124038932 (GRCh38)
11:123909639 (GRCh37)
Canonical SPDI:: NC_000011.10:124038931:G:A,NC_000011.10:124038931:G:C
Gene:: OR10G7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.124038932G>A, NC_000011.10:g.124038932G>C, NC_000011.9:g.123909639G>A, NC_000011.9:g.123909639G>C, NM_001004463.2:c.70C>T, NM_001004463.2:c.70C>G, NM_001004463.1:c.70C>T, NM_001004463.1:c.70C>G, NP_001004463.1:p.Pro24Ser, NP_001004463.1:p.Pro24Ala

Select item 144843196519.

rs1448431965 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:124038848 (GRCh38)
11:123909555 (GRCh37)
Canonical SPDI:: NC_000011.10:124038847:G:A,NC_000011.10:124038847:G:T
Gene:: OR10G7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.124038848G>A, NC_000011.10:g.124038848G>T, NC_000011.9:g.123909555G>A, NC_000011.9:g.123909555G>T, NM_001004463.2:c.154C>T, NM_001004463.2:c.154C>A, NM_001004463.1:c.154C>T, NM_001004463.1:c.154C>A, NP_001004463.1:p.His52Tyr, NP_001004463.1:p.His52Asn

Select item 144823798120.

rs1448237981 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:124038113 (GRCh38)
11:123908820 (GRCh37)
Canonical SPDI:: NC_000011.10:124038112:C:A
Gene:: OR10G7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.124038113C>A, NC_000011.9:g.123908820C>A, NM_001004463.2:c.889G>T, NM_001004463.1:c.889G>T, NP_001004463.1:p.Ala297Ser

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Items: 1 to 20 of 415

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