SNP Links for Protein (Select 52317111) - SNP

Links from Protein

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Select item 14908934211.

rs1490893421 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:59364547 (GRCh38)
11:59132020 (GRCh37)
Canonical SPDI:: NC_000011.10:59364546:C:A,NC_000011.10:59364546:C:T
Gene:: OR5AN1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.59364547C>A, NC_000011.10:g.59364547C>T, NC_000011.9:g.59132020C>A, NC_000011.9:g.59132020C>T, NM_001004729.2:c.89C>A, NM_001004729.2:c.89C>T, NM_001004729.1:c.89C>A, NM_001004729.1:c.89C>T, NP_001004729.1:p.Thr30Asn, NP_001004729.1:p.Thr30Ile

Select item 14892858432.

rs1489285843 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:59364536 (GRCh38)
11:59132009 (GRCh37)
Canonical SPDI:: NC_000011.10:59364535:A:C
Gene:: OR5AN1 (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=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.59364536A>C, NC_000011.9:g.59132009A>C, NM_001004729.2:c.78A>C, NM_001004729.1:c.78A>C, NP_001004729.1:p.Lys26Asn

Select item 14883308963.

rs1488330896 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:59364684 (GRCh38)
11:59132157 (GRCh37)
Canonical SPDI:: NC_000011.10:59364683:A:G
Gene:: OR5AN1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.59364684A>G, NC_000011.9:g.59132157A>G, NM_001004729.2:c.226A>G, NM_001004729.1:c.226A>G, NP_001004729.1:p.Ser76Gly

Select item 14858121864.

rs1485812186 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 11:59364644 (GRCh38)
11:59132117 (GRCh37)
Canonical SPDI:: NC_000011.10:59364643:C:
Gene:: OR5AN1 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.59364644del, NC_000011.9:g.59132117del, NM_001004729.2:c.186del, NM_001004729.1:c.186del, NP_001004729.1:p.Phe63fs

Select item 14708045885.

rs1470804588 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:59365008 (GRCh38)
11:59132481 (GRCh37)
Canonical SPDI:: NC_000011.10:59365007:C:A,NC_000011.10:59365007:C:T
Gene:: OR5AN1 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
T=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000011.10:g.59365008C>A, NC_000011.10:g.59365008C>T, NC_000011.9:g.59132481C>A, NC_000011.9:g.59132481C>T, NM_001004729.2:c.550C>A, NM_001004729.2:c.550C>T, NM_001004729.1:c.550C>A, NM_001004729.1:c.550C>T, NP_001004729.1:p.Gln184Lys, NP_001004729.1:p.Gln184Ter

Select item 14691359676.

rs1469135967 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:59364754 (GRCh38)
11:59132227 (GRCh37)
Canonical SPDI:: NC_000011.10:59364753:T:A
Gene:: OR5AN1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.59364754T>A, NC_000011.9:g.59132227T>A, NM_001004729.2:c.296T>A, NM_001004729.1:c.296T>A, NP_001004729.1:p.Ile99Asn

Select item 14690859097.

rs1469085909 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:59365364 (GRCh38)
11:59132837 (GRCh37)
Canonical SPDI:: NC_000011.10:59365363:A:G
Gene:: OR5AN1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.59365364A>G, NC_000011.9:g.59132837A>G, NM_001004729.2:c.906A>G, NM_001004729.1:c.906A>G

Select item 14665793658.

rs1466579365 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:59364752 (GRCh38)
11:59132225 (GRCh37)
Canonical SPDI:: NC_000011.10:59364751:T:C
Gene:: OR5AN1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.59364752T>C, NC_000011.9:g.59132225T>C, NM_001004729.2:c.294T>C, NM_001004729.1:c.294T>C

Select item 14661030409.

rs1466103040 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTGT [Show Flanks]
Chromosome:: 11:59364993 (GRCh38)
11:59132467 (GRCh37)
Canonical SPDI:: NC_000011.10:59364993:TCTGT:TCTGTCTGT
Gene:: OR5AN1 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_indel,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: TCTGTCTGT=0./0 (ALFA)
TCTG=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.59364995_59364998dup, NC_000011.9:g.59132468_59132471dup, NM_001004729.2:c.537_540dup, NM_001004729.1:c.537_540dup, NP_001004729.1:p.Asp181delinsLeuTer

Select item 146477892110.

rs1464778921 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:59365266 (GRCh38)
11:59132739 (GRCh37)
Canonical SPDI:: NC_000011.10:59365265:A:G
Gene:: OR5AN1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.59365266A>G, NC_000011.9:g.59132739A>G, NM_001004729.2:c.808A>G, NM_001004729.1:c.808A>G, NP_001004729.1:p.Ser270Gly

Select item 145881828811.

rs1458818288 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:59364782 (GRCh38)
11:59132255 (GRCh37)
Canonical SPDI:: NC_000011.10:59364781:G:A
Gene:: OR5AN1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000026/7 (TOPMED)
A=0.000029/4 (GnomAD)
HGVS:: NC_000011.10:g.59364782G>A, NC_000011.9:g.59132255G>A, NM_001004729.2:c.324G>A, NM_001004729.1:c.324G>A, NP_001004729.1:p.Met108Ile

Select item 145490357912.

rs1454903579 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:59364958 (GRCh38)
11:59132431 (GRCh37)
Canonical SPDI:: NC_000011.10:59364957:T:C
Gene:: OR5AN1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.59364958T>C, NC_000011.9:g.59132431T>C, NM_001004729.2:c.500T>C, NM_001004729.1:c.500T>C, NP_001004729.1:p.Leu167Pro

Select item 145360667213.

rs1453606672 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:59365311 (GRCh38)
11:59132784 (GRCh37)
Canonical SPDI:: NC_000011.10:59365310:A:G,NC_000011.10:59365310:A:T
Gene:: OR5AN1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.59365311A>G, NC_000011.10:g.59365311A>T, NC_000011.9:g.59132784A>G, NC_000011.9:g.59132784A>T, NM_001004729.2:c.853A>G, NM_001004729.2:c.853A>T, NM_001004729.1:c.853A>G, NM_001004729.1:c.853A>T, NP_001004729.1:p.Met285Val, NP_001004729.1:p.Met285Leu

Select item 144481278414.

rs1444812784 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:59365272 (GRCh38)
11:59132745 (GRCh37)
Canonical SPDI:: NC_000011.10:59365271:G:C
Gene:: OR5AN1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.59365272G>C, NC_000011.9:g.59132745G>C, NM_001004729.2:c.814G>C, NM_001004729.1:c.814G>C, NP_001004729.1:p.Asp272His

Select item 144122401615.

rs1441224016 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:59365371 (GRCh38)
11:59132844 (GRCh37)
Canonical SPDI:: NC_000011.10:59365370:T:C
Gene:: OR5AN1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.59365371T>C, NC_000011.9:g.59132844T>C, NM_001004729.2:c.913T>C, NM_001004729.1:c.913T>C

Select item 144016472016.

rs1440164720 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:59364820 (GRCh38)
11:59132293 (GRCh37)
Canonical SPDI:: NC_000011.10:59364819:A:G
Gene:: OR5AN1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.59364820A>G, NC_000011.9:g.59132293A>G, NM_001004729.2:c.362A>G, NM_001004729.1:c.362A>G, NP_001004729.1:p.Tyr121Cys

Select item 143953376117.

rs1439533761 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:59365299 (GRCh38)
11:59132772 (GRCh37)
Canonical SPDI:: NC_000011.10:59365298:G:A
Gene:: OR5AN1 (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_000011.10:g.59365299G>A, NC_000011.9:g.59132772G>A, NM_001004729.2:c.841G>A, NM_001004729.1:c.841G>A, NP_001004729.1:p.Val281Met

Select item 143853093118.

rs1438530931 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:59365069 (GRCh38)
11:59132542 (GRCh37)
Canonical SPDI:: NC_000011.10:59365068:C:T
Gene:: OR5AN1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.59365069C>T, NC_000011.9:g.59132542C>T, NM_001004729.2:c.611C>T, NM_001004729.1:c.611C>T, NP_001004729.1:p.Thr204Ile

Select item 143765385719.

rs1437653857 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:59364837 (GRCh38)
11:59132310 (GRCh37)
Canonical SPDI:: NC_000011.10:59364836:A:G
Gene:: OR5AN1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.59364837A>G, NC_000011.9:g.59132310A>G, NM_001004729.2:c.379A>G, NM_001004729.1:c.379A>G, NP_001004729.1:p.Ile127Val

Select item 143568987120.

rs1435689871 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:59364839 (GRCh38)
11:59132312 (GRCh37)
Canonical SPDI:: NC_000011.10:59364838:T:C
Gene:: OR5AN1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.59364839T>C, NC_000011.9:g.59132312T>C, NM_001004729.2:c.381T>C, NM_001004729.1:c.381T>C

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Items: 1 to 20 of 365

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