SNP Links for Nucleotide (Select 52627159) - SNP

Links from Nucleotide

Items: 1 to 20 of 385

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Select item 14890559031.

rs1489055903 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:55221480 (GRCh38)
12:55615264 (GRCh37)
Canonical SPDI:: NC_000012.12:55221479:T:C
Gene:: OR10A7 (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)
C=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.55221480T>C, NC_000012.11:g.55615264T>C, NM_001005280.1:c.456T>C

Select item 14886681172.

rs1488668117 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:55221375 (GRCh38)
12:55615159 (GRCh37)
Canonical SPDI:: NC_000012.12:55221374:G:A
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: A=0.0003/1 (KOREAN)
HGVS:: NC_000012.12:g.55221375G>A, NC_000012.11:g.55615159G>A, NM_001005280.1:c.351G>A, NP_001005280.1:p.Met117Ile

Select item 14862555743.

rs1486255574 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 12:55221594 (GRCh38)
12:55615378 (GRCh37)
Canonical SPDI:: NC_000012.12:55221593:G:A,NC_000012.12:55221593:G:C
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000012.12:g.55221594G>A, NC_000012.12:g.55221594G>C, NC_000012.11:g.55615378G>A, NC_000012.11:g.55615378G>C, NM_001005280.1:c.570G>A, NM_001005280.1:c.570G>C

Select item 14832811924.

rs1483281192 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:55221777 (GRCh38)
12:55615561 (GRCh37)
Canonical SPDI:: NC_000012.12:55221776:C:T
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000051/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55221777C>T, NC_000012.11:g.55615561C>T, NM_001005280.1:c.753C>T

Select item 14826326155.

rs1482632615 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:55221254 (GRCh38)
12:55615038 (GRCh37)
Canonical SPDI:: NC_000012.12:55221253:T:C
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55221254T>C, NC_000012.11:g.55615038T>C, NM_001005280.1:c.230T>C, NP_001005280.1:p.Met77Thr

Select item 14801498616.

rs1480149861 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:55221659 (GRCh38)
12:55615443 (GRCh37)
Canonical SPDI:: NC_000012.12:55221658:G:A
Gene:: OR10A7 (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=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.55221659G>A, NC_000012.11:g.55615443G>A, NM_001005280.1:c.635G>A, NP_001005280.1:p.Cys212Tyr

Select item 14795382487.

rs1479538248 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:55221465 (GRCh38)
12:55615249 (GRCh37)
Canonical SPDI:: NC_000012.12:55221464:C:T
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000012.12:g.55221465C>T, NC_000012.11:g.55615249C>T, NM_001005280.1:c.441C>T

Select item 14737861628.

rs1473786162 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:55221523 (GRCh38)
12:55615307 (GRCh37)
Canonical SPDI:: NC_000012.12:55221522:C:T
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
T=0.000022/3 (GnomAD)
HGVS:: NC_000012.12:g.55221523C>T, NC_000012.11:g.55615307C>T, NM_001005280.1:c.499C>T, NP_001005280.1:p.Pro167Ser

Select item 14704144859.

rs1470414485 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:55221128 (GRCh38)
12:55614912 (GRCh37)
Canonical SPDI:: NC_000012.12:55221127:A:G
Gene:: OR10A7 (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=0.000008/2 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000012.12:g.55221128A>G, NC_000012.11:g.55614912A>G, NM_001005280.1:c.104A>G, NP_001005280.1:p.Tyr35Cys

Select item 146930500010.

rs1469305000 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:55221383 (GRCh38)
12:55615167 (GRCh37)
Canonical SPDI:: NC_000012.12:55221382:A:G
Gene:: OR10A7 (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=0.000015/4 (TOPMED)
G=0.000043/6 (GnomAD)
HGVS:: NC_000012.12:g.55221383A>G, NC_000012.11:g.55615167A>G, NM_001005280.1:c.359A>G, NP_001005280.1:p.Tyr120Cys

Select item 146929930711.

rs1469299307 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:55221959 (GRCh38)
12:55615743 (GRCh37)
Canonical SPDI:: NC_000012.12:55221958:A:G
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55221959A>G, NC_000012.11:g.55615743A>G, NM_001005280.1:c.935A>G, NP_001005280.1:p.Lys312Arg

Select item 146841937012.

rs1468419370 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:55221782 (GRCh38)
12:55615566 (GRCh37)
Canonical SPDI:: NC_000012.12:55221781:G:A
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000224/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000223/1 (Estonian)
HGVS:: NC_000012.12:g.55221782G>A, NC_000012.11:g.55615566G>A, NM_001005280.1:c.758G>A, NP_001005280.1:p.Gly253Glu

Select item 146672213813.

rs1466722138 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:55221883 (GRCh38)
12:55615667 (GRCh37)
Canonical SPDI:: NC_000012.12:55221882:C:T
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000012.12:g.55221883C>T, NC_000012.11:g.55615667C>T, NM_001005280.1:c.859C>T, NP_001005280.1:p.Pro287Ser

Select item 146662717414.

rs1466627174 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:55221930 (GRCh38)
12:55615714 (GRCh37)
Canonical SPDI:: NC_000012.12:55221929:G:A
Gene:: OR10A7 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55221930G>A, NC_000012.11:g.55615714G>A, NM_001005280.1:c.906G>A

Select item 146582447515.

rs1465824475 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 12:55221374 (GRCh38)
12:55615158 (GRCh37)
Canonical SPDI:: NC_000012.12:55221373:T:A,NC_000012.12:55221373:T:C
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.55221374T>A, NC_000012.12:g.55221374T>C, NC_000012.11:g.55615158T>A, NC_000012.11:g.55615158T>C, NM_001005280.1:c.350T>A, NM_001005280.1:c.350T>C, NP_001005280.1:p.Met117Lys, NP_001005280.1:p.Met117Thr

Select item 146571712616.

rs1465717126 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 12:55221344 (GRCh38)
12:55615128 (GRCh37)
Canonical SPDI:: NC_000012.12:55221343:T:C,NC_000012.12:55221343:T:G
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55221344T>C, NC_000012.12:g.55221344T>G, NC_000012.11:g.55615128T>C, NC_000012.11:g.55615128T>G, NM_001005280.1:c.320T>C, NM_001005280.1:c.320T>G, NP_001005280.1:p.Phe107Ser, NP_001005280.1:p.Phe107Cys

Select item 145814323117.

rs1458143231 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:55221771 (GRCh38)
12:55615555 (GRCh37)
Canonical SPDI:: NC_000012.12:55221770:C:T
Gene:: OR10A7 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000043/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.55221771C>T, NC_000012.11:g.55615555C>T, NM_001005280.1:c.747C>T

Select item 145596801418.

rs1455968014 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 12:55221208 (GRCh38)
12:55614992 (GRCh37)
Canonical SPDI:: NC_000012.12:55221207:TTT:TT
Gene:: OR10A7 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
-=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.55221210del, NC_000012.11:g.55614994del, NM_001005280.1:c.186del, NP_001005280.1:p.Leu63fs

Select item 145589075519.

rs1455890755 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 12:55221746 (GRCh38)
12:55615530 (GRCh37)
Canonical SPDI:: NC_000012.12:55221745:G:A,NC_000012.12:55221745:G:T
Gene:: OR10A7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.55221746G>A, NC_000012.12:g.55221746G>T, NC_000012.11:g.55615530G>A, NC_000012.11:g.55615530G>T, NM_001005280.1:c.722G>A, NM_001005280.1:c.722G>T, NP_001005280.1:p.Cys241Tyr, NP_001005280.1:p.Cys241Phe

Select item 145537870920.

rs1455378709 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:55221046 (GRCh38)
12:55614830 (GRCh37)
Canonical SPDI:: NC_000012.12:55221045:A:G
Gene:: OR10A7 (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=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.55221046A>G, NC_000012.11:g.55614830A>G, NM_001005280.1:c.22A>G, NP_001005280.1:p.Arg8Gly

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Items: 1 to 20 of 385

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