SNP Links for Protein (Select 52546741) - SNP

Links from Protein

Items: 1 to 20 of 356

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Select item 14796874761.

rs1479687476 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:56542419 (GRCh38)
11:56309895 (GRCh37)
Canonical SPDI:: NC_000011.10:56542418:A:G
Gene:: OR5M11 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.56542419A>G, NC_000011.9:g.56309895A>G, NM_001005245.1:c.839T>C, NP_001005245.1:p.Val280Ala

Select item 14766404652.

rs1476640465 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:56543192 (GRCh38)
11:56310668 (GRCh37)
Canonical SPDI:: NC_000011.10:56543191:T:G
Gene:: OR5M11 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000132/2 (ALFA)
G=0.000029/4 (GnomAD)
G=0.000446/2 (Estonian)
HGVS:: NC_000011.10:g.56543192T>G, NC_000011.9:g.56310668T>G, NM_001005245.1:c.66A>C, NP_001005245.1:p.Glu22Asp

Select item 14591965833.

rs1459196583 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:56542667 (GRCh38)
11:56310143 (GRCh37)
Canonical SPDI:: NC_000011.10:56542666:G:A
Gene:: OR5M11 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.56542667G>A, NC_000011.9:g.56310143G>A, NM_001005245.1:c.591C>T

Select item 14533498904.

rs1453349890 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:56542484 (GRCh38)
11:56309960 (GRCh37)
Canonical SPDI:: NC_000011.10:56542483:A:G
Gene:: OR5M11 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.56542484A>G, NC_000011.9:g.56309960A>G, NM_001005245.1:c.774T>C

Select item 14521857725.

rs1452185772 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:56542974 (GRCh38)
11:56310450 (GRCh37)
Canonical SPDI:: NC_000011.10:56542973:C:A
Gene:: OR5M11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.56542974C>A, NC_000011.9:g.56310450C>A, NM_001005245.1:c.284G>T, NP_001005245.1:p.Gly95Val

Select item 14497562466.

rs1449756246 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:56542598 (GRCh38)
11:56310074 (GRCh37)
Canonical SPDI:: NC_000011.10:56542597:A:T
Gene:: OR5M11 (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_000011.10:g.56542598A>T, NC_000011.9:g.56310074A>T, NM_001005245.1:c.660T>A

Select item 14398098777.

rs1439809877 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:56543204 (GRCh38)
11:56310680 (GRCh37)
Canonical SPDI:: NC_000011.10:56543203:T:G
Gene:: OR5M11 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.56543204T>G, NC_000011.9:g.56310680T>G, NM_001005245.1:c.54A>C

Select item 14353236998.

rs1435323699 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:56542690 (GRCh38)
11:56310166 (GRCh37)
Canonical SPDI:: NC_000011.10:56542689:C:A
Gene:: OR5M11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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.56542690C>A, NC_000011.9:g.56310166C>A, NM_001005245.1:c.568G>T, NP_001005245.1:p.Asp190Tyr

Select item 14252191559.

rs1425219155 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:56542370 (GRCh38)
11:56309846 (GRCh37)
Canonical SPDI:: NC_000011.10:56542369:C:A
Gene:: OR5M11 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.56542370C>A, NC_000011.9:g.56309846C>A, NM_001005245.1:c.888G>T

Select item 142392781110.

rs1423927811 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:56543220 (GRCh38)
11:56310696 (GRCh37)
Canonical SPDI:: NC_000011.10:56543219:A:C
Gene:: OR5M11 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.56543220A>C, NC_000011.9:g.56310696A>C, NM_001005245.1:c.38T>G, NP_001005245.1:p.Ile13Ser

Select item 141850958011.

rs1418509580 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:56542522 (GRCh38)
11:56309998 (GRCh37)
Canonical SPDI:: NC_000011.10:56542521:C:A,NC_000011.10:56542521:C:T
Gene:: OR5M11 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.56542522C>A, NC_000011.10:g.56542522C>T, NC_000011.9:g.56309998C>A, NC_000011.9:g.56309998C>T, NM_001005245.1:c.736G>T, NM_001005245.1:c.736G>A, NP_001005245.1:p.Ala246Ser, NP_001005245.1:p.Ala246Thr

Select item 141725685412.

rs1417256854 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 11:56543085 (GRCh38)
11:56310561 (GRCh37)
Canonical SPDI:: NC_000011.10:56543084:G:C,NC_000011.10:56543084:G:T
Gene:: OR5M11 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.56543085G>C, NC_000011.10:g.56543085G>T, NC_000011.9:g.56310561G>C, NC_000011.9:g.56310561G>T, NM_001005245.1:c.173C>G, NM_001005245.1:c.173C>A, NP_001005245.1:p.Pro58Arg, NP_001005245.1:p.Pro58His

Select item 141579190113.

rs1415791901 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:56542823 (GRCh38)
11:56310299 (GRCh37)
Canonical SPDI:: NC_000011.10:56542822:T:A,NC_000011.10:56542822:T:C
Gene:: OR5M11 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.56542823T>A, NC_000011.10:g.56542823T>C, NC_000011.9:g.56310299T>A, NC_000011.9:g.56310299T>C, NM_001005245.1:c.435A>T, NM_001005245.1:c.435A>G

Select item 141357100214.

rs1413571002 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:56542804 (GRCh38)
11:56310280 (GRCh37)
Canonical SPDI:: NC_000011.10:56542803:A:C
Gene:: OR5M11 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0.0001/1 (ALFA)
HGVS:: NC_000011.10:g.56542804A>C, NC_000011.9:g.56310280A>C, NM_001005245.1:c.454T>G, NP_001005245.1:p.Phe152Val

Select item 141215318015.

rs1412153180 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:56543197 (GRCh38)
11:56310673 (GRCh37)
Canonical SPDI:: NC_000011.10:56543196:G:A
Gene:: OR5M11 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (GnomAD)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.56543197G>A, NC_000011.9:g.56310673G>A, NM_001005245.1:c.61C>T, NP_001005245.1:p.Pro21Ser

Select item 140787006416.

rs1407870064 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:56542608 (GRCh38)
11:56310084 (GRCh37)
Canonical SPDI:: NC_000011.10:56542607:T:C
Gene:: OR5M11 (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_000011.10:g.56542608T>C, NC_000011.9:g.56310084T>C, NM_001005245.1:c.650A>G, NP_001005245.1:p.Tyr217Cys

Select item 139442572217.

rs1394425722 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:56542989 (GRCh38)
11:56310465 (GRCh37)
Canonical SPDI:: NC_000011.10:56542988:G:A,NC_000011.10:56542988:G:T
Gene:: OR5M11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000224/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
A=0.000223/1 (Estonian)
HGVS:: NC_000011.10:g.56542989G>A, NC_000011.10:g.56542989G>T, NC_000011.9:g.56310465G>A, NC_000011.9:g.56310465G>T, NM_001005245.1:c.269C>T, NM_001005245.1:c.269C>A, NP_001005245.1:p.Thr90Ile, NP_001005245.1:p.Thr90Asn

Select item 139426005618.

rs1394260056 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:56542881 (GRCh38)
11:56310357 (GRCh37)
Canonical SPDI:: NC_000011.10:56542880:T:C
Gene:: OR5M11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000051/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.56542881T>C, NC_000011.9:g.56310357T>C, NM_001005245.1:c.377A>G, NP_001005245.1:p.Tyr126Cys

Select item 139044776719.

rs1390447767 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:56542714 (GRCh38)
11:56310190 (GRCh37)
Canonical SPDI:: NC_000011.10:56542713:G:A
Gene:: OR5M11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000011.10:g.56542714G>A, NC_000011.9:g.56310190G>A, NM_001005245.1:c.544C>T, NP_001005245.1:p.Pro182Ser

Select item 138932849220.

rs1389328492 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:56543161 (GRCh38)
11:56310637 (GRCh37)
Canonical SPDI:: NC_000011.10:56543160:C:T
Gene:: OR5M11 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.56543161C>T, NC_000011.9:g.56310637C>T, NM_001005245.1:c.97G>A, NP_001005245.1:p.Val33Ile

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