SNP Links for Protein (Select 53828666) - SNP

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Links from Protein

Items: 1 to 20 of 353

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Select item 14885820081.

rs1488582008 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 12:55637193 (GRCh38)
12:56030977 (GRCh37)
Canonical SPDI:: NC_000012.12:55637192:A:T
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55637193A>T, NC_000012.11:g.56030977A>T, NM_206899.1:c.302A>T, NP_996782.1:p.Gln101Leu

Select item 14755433382.

rs1475543338 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:55637687 (GRCh38)
12:56031471 (GRCh37)
Canonical SPDI:: NC_000012.12:55637686:G:A
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55637687G>A, NC_000012.11:g.56031471G>A, NM_206899.1:c.796G>A, NP_996782.1:p.Gly266Ser

Select item 14754808443.

rs1475480844 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 12:55637292 (GRCh38)
12:56031076 (GRCh37)
Canonical SPDI:: NC_000012.12:55637291:C:G
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000042/11 (TOPMED)
G=0.000078/11 (GnomAD)
HGVS:: NC_000012.12:g.55637292C>G, NC_000012.11:g.56031076C>G, NM_206899.1:c.401C>G, NP_996782.1:p.Ser134Cys

Select item 14747947904.

rs1474794790 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:55637768 (GRCh38)
12:56031552 (GRCh37)
Canonical SPDI:: NC_000012.12:55637767:C:T
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55637768C>T, NC_000012.11:g.56031552C>T, NM_206899.1:c.877C>T, NP_996782.1:p.Leu293Phe

Select item 14745148965.

rs1474514896 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:55637629 (GRCh38)
12:56031413 (GRCh37)
Canonical SPDI:: NC_000012.12:55637628:G:A
Gene:: OR10P1 (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_000012.12:g.55637629G>A, NC_000012.11:g.56031413G>A, NM_206899.1:c.738G>A

Select item 14724650816.

rs1472465081 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:55637084 (GRCh38)
12:56030868 (GRCh37)
Canonical SPDI:: NC_000012.12:55637083:C:T
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.55637084C>T, NC_000012.11:g.56030868C>T, NM_206899.1:c.193C>T, NP_996782.1:p.Gln65Ter

Select item 14685379267.

rs1468537926 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:55637197 (GRCh38)
12:56030981 (GRCh37)
Canonical SPDI:: NC_000012.12:55637196:G:A
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.55637197G>A, NC_000012.11:g.56030981G>A, NM_206899.1:c.306G>A, NP_996782.1:p.Met102Ile

Select item 14656847878.

rs1465684787 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:55637625 (GRCh38)
12:56031409 (GRCh37)
Canonical SPDI:: NC_000012.12:55637624:A:G
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55637625A>G, NC_000012.11:g.56031409A>G, NM_206899.1:c.734A>G, NP_996782.1:p.His245Arg

Select item 14627128969.

rs1462712896 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 12:55637557 (GRCh38)
12:56031341 (GRCh37)
Canonical SPDI:: NC_000012.12:55637556:C:A
Gene:: OR10P1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55637557C>A, NC_000012.11:g.56031341C>A, NM_206899.1:c.666C>A

Select item 145839275710.

rs1458392757 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:55636973 (GRCh38)
12:56030757 (GRCh37)
Canonical SPDI:: NC_000012.12:55636972:T:C
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55636973T>C, NC_000012.11:g.56030757T>C, NM_206899.1:c.82T>C, NP_996782.1:p.Phe28Leu

Select item 145374402011.

rs1453744020 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:55637619 (GRCh38)
12:56031403 (GRCh37)
Canonical SPDI:: NC_000012.12:55637618:C:T
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.55637619C>T, NC_000012.11:g.56031403C>T, NM_206899.1:c.728C>T, NP_996782.1:p.Ser243Phe

Select item 145122730212.

rs1451227302 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:55637125 (GRCh38)
12:56030909 (GRCh37)
Canonical SPDI:: NC_000012.12:55637124:G:A
Gene:: OR10P1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.55637125G>A, NC_000012.11:g.56030909G>A, NM_206899.1:c.234G>A

Select item 144694578213.

rs1446945782 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:55637577 (GRCh38)
12:56031361 (GRCh37)
Canonical SPDI:: NC_000012.12:55637576:T:C
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55637577T>C, NC_000012.11:g.56031361T>C, NM_206899.1:c.686T>C, NP_996782.1:p.Met229Thr

Select item 144601400814.

rs1446014008 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:55637200 (GRCh38)
12:56030984 (GRCh37)
Canonical SPDI:: NC_000012.12:55637199:C:T
Gene:: OR10P1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.55637200C>T, NC_000012.11:g.56030984C>T, NM_206899.1:c.309C>T

Select item 144350790015.

rs1443507900 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 12:55637450 (GRCh38)
12:56031234 (GRCh37)
Canonical SPDI:: NC_000012.12:55637449:A:C
Gene:: OR10P1 (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=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.55637450A>C, NC_000012.11:g.56031234A>C, NM_206899.1:c.559A>C

Select item 144238269916.

rs1442382699 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:55637500 (GRCh38)
12:56031284 (GRCh37)
Canonical SPDI:: NC_000012.12:55637499:C:T
Gene:: OR10P1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55637500C>T, NC_000012.11:g.56031284C>T, NM_206899.1:c.609C>T

Select item 144214166517.

rs1442141665 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CT [Show Flanks]
Chromosome:: 12:55637636 (GRCh38)
12:56031421 (GRCh37)
Canonical SPDI:: NC_000012.12:55637636:TCTCTCTCT:TCTCTCTCTCT
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: TC=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55637638CT[5], NC_000012.11:g.56031422CT[5], NM_206899.1:c.753_754dup, NP_996782.1:p.Phe252fs

Select item 144090602218.

rs1440906022 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:55637013 (GRCh38)
12:56030797 (GRCh37)
Canonical SPDI:: NC_000012.12:55637012:G:A
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55637013G>A, NC_000012.11:g.56030797G>A, NM_206899.1:c.122G>A, NP_996782.1:p.Gly41Asp

Select item 144038926919.

rs1440389269 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:55636909 (GRCh38)
12:56030693 (GRCh37)
Canonical SPDI:: NC_000012.12:55636908:T:C
Gene:: OR10P1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000012.12:g.55636909T>C, NC_000012.11:g.56030693T>C, NM_206899.1:c.18T>C

Select item 143840616520.

rs1438406165 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:55636938 (GRCh38)
12:56030722 (GRCh37)
Canonical SPDI:: NC_000012.12:55636937:G:A
Gene:: OR10P1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
A=0.000035/1 (TOMMO)
HGVS:: NC_000012.12:g.55636938G>A, NC_000012.11:g.56030722G>A, NM_206899.1:c.47G>A, NP_996782.1:p.Gly16Glu

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