SNP Links for Protein (Select 237858660) - SNP

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Links from Protein

Items: 1 to 20 of 378

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Select item 14884036031.

rs1488403603 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:158562945 (GRCh38)
1:158532735 (GRCh37)
Canonical SPDI:: NC_000001.11:158562944:G:T
Gene:: OR6P1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.158562945G>T, NC_000001.10:g.158532735G>T, NM_001160325.2:c.660C>A, NM_001160325.1:c.660C>A

Select item 14856731422.

rs1485673142 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:158562659 (GRCh38)
1:158532449 (GRCh37)
Canonical SPDI:: NC_000001.11:158562658:G:A
Gene:: OR6P1 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.158562659G>A, NC_000001.10:g.158532449G>A, NM_001160325.2:c.946C>T, NM_001160325.1:c.946C>T, NP_001153797.1:p.Gln316Ter

Select item 14851676183.

rs1485167618 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:158562673 (GRCh38)
1:158532463 (GRCh37)
Canonical SPDI:: NC_000001.11:158562672:T:C
Gene:: OR6P1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.158562673T>C, NC_000001.10:g.158532463T>C, NM_001160325.2:c.932A>G, NM_001160325.1:c.932A>G, NP_001153797.1:p.Tyr311Cys

Select item 14848912264.

rs1484891226 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:158563524 (GRCh38)
1:158533314 (GRCh37)
Canonical SPDI:: NC_000001.11:158563523:G:C
Gene:: OR6P1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.158563524G>C, NC_000001.10:g.158533314G>C, NM_001160325.2:c.81C>G, NM_001160325.1:c.81C>G

Select item 14848076255.

rs1484807625 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:158562735 (GRCh38)
1:158532525 (GRCh37)
Canonical SPDI:: NC_000001.11:158562734:G:A
Gene:: OR6P1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.158562735G>A, NC_000001.10:g.158532525G>A, NM_001160325.2:c.870C>T, NM_001160325.1:c.870C>T

Select item 14829589476.

rs1482958947 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 1:158562840 (GRCh38)
1:158532630 (GRCh37)
Canonical SPDI:: NC_000001.11:158562839:A:C,NC_000001.11:158562839:A:G,NC_000001.11:158562839:A:T
Gene:: OR6P1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000001.11:g.158562840A>C, NC_000001.11:g.158562840A>G, NC_000001.11:g.158562840A>T, NC_000001.10:g.158532630A>C, NC_000001.10:g.158532630A>G, NC_000001.10:g.158532630A>T, NM_001160325.2:c.765T>G, NM_001160325.2:c.765T>C, NM_001160325.2:c.765T>A, NM_001160325.1:c.765T>G, NM_001160325.1:c.765T>C, NM_001160325.1:c.765T>A

Select item 14812373807.

rs1481237380 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TGGTTG [Show Flanks]
Chromosome:: 1:158562791 (GRCh38)
1:158532582 (GRCh37)
Canonical SPDI:: NC_000001.11:158562791:GTTGTGGTTG:GTTGTGGTTGTGGTTG
Gene:: OR6P1 (Varview)
Functional Consequence:: inframe_insertion,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTTGTGGTTGTGGTTG=0./0 (ALFA)
GTTGTG=0.000007/1 (GnomAD)
GTTGTG=0.000008/2 (TOPMED)
GTTGTG=0.000056/9 (GnomAD_exomes)
HGVS:: NC_000001.11:g.158562796_158562801dup, NC_000001.10:g.158532586_158532591dup, NM_001160325.2:c.808_813dup, NM_001160325.1:c.808_813dup, NP_001153797.1:p.His270_Asn271dup

Select item 14788051058.

rs1478805105 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 1:158562857 (GRCh38)
1:158532647 (GRCh37)
Canonical SPDI:: NC_000001.11:158562856:T:A,NC_000001.11:158562856:T:C
Gene:: OR6P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.158562857T>A, NC_000001.11:g.158562857T>C, NC_000001.10:g.158532647T>A, NC_000001.10:g.158532647T>C, NM_001160325.2:c.748A>T, NM_001160325.2:c.748A>G, NM_001160325.1:c.748A>T, NM_001160325.1:c.748A>G, NP_001153797.1:p.Ile250Phe, NP_001153797.1:p.Ile250Val

Select item 14787525229.

rs1478752522 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:158563532 (GRCh38)
1:158533322 (GRCh37)
Canonical SPDI:: NC_000001.11:158563531:G:C
Gene:: OR6P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.158563532G>C, NC_000001.10:g.158533322G>C, NM_001160325.2:c.73C>G, NM_001160325.1:c.73C>G, NP_001153797.1:p.Leu25Val

Select item 147756031710.

rs1477560317 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:158563214 (GRCh38)
1:158533004 (GRCh37)
Canonical SPDI:: NC_000001.11:158563213:G:A,NC_000001.11:158563213:G:T
Gene:: OR6P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.158563214G>A, NC_000001.11:g.158563214G>T, NC_000001.10:g.158533004G>A, NC_000001.10:g.158533004G>T, NM_001160325.2:c.391C>T, NM_001160325.2:c.391C>A, NM_001160325.1:c.391C>T, NM_001160325.1:c.391C>A, NP_001153797.1:p.Leu131Phe, NP_001153797.1:p.Leu131Ile

Select item 147666500711.

rs1476665007 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:158562831 (GRCh38)
1:158532621 (GRCh37)
Canonical SPDI:: NC_000001.11:158562830:G:T
Gene:: OR6P1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.158562831G>T, NC_000001.10:g.158532621G>T, NM_001160325.2:c.774C>A, NM_001160325.1:c.774C>A

Select item 147484846512.

rs1474848465 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:158562951 (GRCh38)
1:158532741 (GRCh37)
Canonical SPDI:: NC_000001.11:158562950:G:A,NC_000001.11:158562950:G:C
Gene:: OR6P1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
C=0.000026/4 (GnomAD_exomes)
HGVS:: NC_000001.11:g.158562951G>A, NC_000001.11:g.158562951G>C, NC_000001.10:g.158532741G>A, NC_000001.10:g.158532741G>C, NM_001160325.2:c.654C>T, NM_001160325.2:c.654C>G, NM_001160325.1:c.654C>T, NM_001160325.1:c.654C>G, NP_001153797.1:p.Tyr218Ter

Select item 147047638813.

rs1470476388 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:158563314 (GRCh38)
1:158533104 (GRCh37)
Canonical SPDI:: NC_000001.11:158563313:G:T
Gene:: OR6P1 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.158563314G>T, NC_000001.10:g.158533104G>T, NM_001160325.2:c.291C>A, NM_001160325.1:c.291C>A, NP_001153797.1:p.Cys97Ter

Select item 146845338314.

rs1468453383 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:158562962 (GRCh38)
1:158532752 (GRCh37)
Canonical SPDI:: NC_000001.11:158562961:C:G
Gene:: OR6P1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.158562962C>G, NC_000001.10:g.158532752C>G, NM_001160325.2:c.643G>C, NM_001160325.1:c.643G>C, NP_001153797.1:p.Val215Leu

Select item 146839770115.

rs1468397701 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:158563258 (GRCh38)
1:158533048 (GRCh37)
Canonical SPDI:: NC_000001.11:158563257:G:T
Gene:: OR6P1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000169/2 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000023/6 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.158563258G>T, NC_000001.10:g.158533048G>T, NM_001160325.2:c.347C>A, NM_001160325.1:c.347C>A, NP_001153797.1:p.Ala116Glu

Select item 146835134816.

rs1468351348 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:158562850 (GRCh38)
1:158532640 (GRCh37)
Canonical SPDI:: NC_000001.11:158562849:T:G
Gene:: OR6P1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000006/1 (GnomAD_exomes)
G=0.001638/3 (Korea1K)
HGVS:: NC_000001.11:g.158562850T>G, NC_000001.10:g.158532640T>G, NM_001160325.2:c.755A>C, NM_001160325.1:c.755A>C, NP_001153797.1:p.Tyr252Ser

Select item 146666352017.

rs1466663520 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:158563069 (GRCh38)
1:158532859 (GRCh37)
Canonical SPDI:: NC_000001.11:158563068:C:T
Gene:: OR6P1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000056/2 (ALFA)
T=0.000006/1 (GnomAD_exomes)
T=0.000021/3 (GnomAD)
T=0.00003/8 (TOPMED)
HGVS:: NC_000001.11:g.158563069C>T, NC_000001.10:g.158532859C>T, NM_001160325.2:c.536G>A, NM_001160325.1:c.536G>A, NP_001153797.1:p.Cys179Tyr

Select item 146610214918.

rs1466102149 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:158562862 (GRCh38)
1:158532652 (GRCh37)
Canonical SPDI:: NC_000001.11:158562861:A:G
Gene:: OR6P1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000028/1 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000013/2 (GnomAD_exomes)
G=0.000021/3 (GnomAD)
HGVS:: NC_000001.11:g.158562862A>G, NC_000001.10:g.158532652A>G, NM_001160325.2:c.743T>C, NM_001160325.1:c.743T>C, NP_001153797.1:p.Val248Ala

Select item 146307682719.

rs1463076827 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:158563306 (GRCh38)
1:158533096 (GRCh37)
Canonical SPDI:: NC_000001.11:158563305:T:G
Gene:: OR6P1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.158563306T>G, NC_000001.10:g.158533096T>G, NM_001160325.2:c.299A>C, NM_001160325.1:c.299A>C, NP_001153797.1:p.Gln100Pro

Select item 146085271320.

rs1460852713 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:158562909 (GRCh38)
1:158532699 (GRCh37)
Canonical SPDI:: NC_000001.11:158562908:C:T
Gene:: OR6P1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.158562909C>T, NC_000001.10:g.158532699C>T, NM_001160325.2:c.696G>A, NM_001160325.1:c.696G>A