SNP Links for Protein (Select 53933280) - SNP

Links from Protein

Items: 1 to 20 of 168

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Select item 14885848111.

rs1488584811 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:50033631 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033630:A:G
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000121/17 (GnomAD)
HGVS:: NC_000011.10:g.50033631A>G, NW_003571045.1:g.192522A>G, NW_017363816.1:g.75257A>G, NR_160275.1:n.758A>G, NM_001005513.1:c.758A>G

Select item 14854563382.

rs1485456338 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:50033615 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033614:C:T
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.50033615C>T, NW_003571045.1:g.192506C>T, NW_017363816.1:g.75241C>T, NR_160275.1:n.742C>T, NM_001005513.1:c.742C>T

Select item 14849825743.

rs1484982574 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:50033218 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033217:C:T
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000035/1 (TOMMO)
T=0.000057/8 (GnomAD)
T=0.000068/18 (TOPMED)
HGVS:: NC_000011.10:g.50033218C>T, NW_003571045.1:g.192109C>T, NW_017363816.1:g.74844C>T, NR_160275.1:n.345C>T, NM_001005513.1:c.345C>T

Select item 14849523184.

rs1484952318 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:50033293 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033292:G:A
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_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.50033293G>A, NW_003571045.1:g.192184G>A, NW_017363816.1:g.74919G>A, NR_160275.1:n.420G>A, NM_001005513.1:c.420G>A

Select item 14843148335.

rs1484314833 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:50033700 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033699:T:G
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.006904/97 (ALFA)
G=0.007808/50 (1000Genomes)
G=0.009097/1273 (GnomAD)
G=0.009116/2413 (TOPMED)
HGVS:: NC_000011.10:g.50033700T>G, NW_003571045.1:g.192591T>G, NW_017363816.1:g.75326T>G, NR_160275.1:n.827T>G, NM_001005513.1:c.827T>G

Select item 14797602596.

rs1479760259 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:50033787 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033786:A:T
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
T=0.000468/3 (1000Genomes)
HGVS:: NC_000011.10:g.50033787A>T, NW_003571045.1:g.192678A>T, NW_017363816.1:g.75413A>T, NR_160275.1:n.914A>T, NM_001005513.1:c.914A>T

Select item 14784573017.

rs1478457301 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:50033186 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033185:G:C
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000011.10:g.50033186G>C, NW_003571045.1:g.192077G>C, NW_017363816.1:g.74812G>C, NR_160275.1:n.313G>C, NM_001005513.1:c.313G>C

Select item 14780846838.

rs1478084683 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:50033693 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033692:A:G
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_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.50033693A>G, NW_003571045.1:g.192584A>G, NW_017363816.1:g.75319A>G, NR_160275.1:n.820A>G, NM_001005513.1:c.820A>G

Select item 14765180589.

rs1476518058 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:50033285 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033284:T:C
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.50033285T>C, NW_003571045.1:g.192176T>C, NW_017363816.1:g.74911T>C, NR_160275.1:n.412T>C, NM_001005513.1:c.412T>C

Select item 147609547810.

rs1476095478 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:50032909 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50032908:C:T
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000142/2 (ALFA)
T=0.000026/7 (TOPMED)
T=0.000029/4 (GnomAD)
HGVS:: NC_000011.10:g.50032909C>T, NW_003571045.1:g.191800C>T, NW_017363816.1:g.74535C>T, NR_160275.1:n.36C>T, NM_001005513.1:c.36C>T

Select item 147445812111.

rs1474458121 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:50033407 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033406:T:A,NC_000011.10:50033406:T:C
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.50033407T>A, NC_000011.10:g.50033407T>C, NW_003571045.1:g.192298T>A, NW_003571045.1:g.192298T>C, NW_017363816.1:g.75033T>A, NW_017363816.1:g.75033T>C, NR_160275.1:n.534T>A, NR_160275.1:n.534T>C, NM_001005513.1:c.534T>A, NM_001005513.1:c.534T>C

Select item 147007811912.

rs1470078119 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:50033432 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033431:A:G,NC_000011.10:50033431:A:T
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.00047/3 (1000Genomes)
HGVS:: NC_000011.10:g.50033432A>G, NC_000011.10:g.50033432A>T, NW_003571045.1:g.192323A>G, NW_003571045.1:g.192323A>T, NW_017363816.1:g.75058A>G, NW_017363816.1:g.75058A>T, NR_160275.1:n.559A>G, NR_160275.1:n.559A>T, NM_001005513.1:c.559A>G, NM_001005513.1:c.559A>T

Select item 146908678113.

rs1469086781 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:50033055 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033054:T:A
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.50033055T>A, NW_003571045.1:g.191946T>A, NW_017363816.1:g.74681T>A, NR_160275.1:n.182T>A, NM_001005513.1:c.182T>A

Select item 146817038414.

rs1468170384 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:50032944 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50032943:T:C
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.50032944T>C, NW_003571045.1:g.191835T>C, NW_017363816.1:g.74570T>C, NR_160275.1:n.71T>C, NM_001005513.1:c.71T>C

Select item 146686684915.

rs1466866849 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:50033549 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033548:G:C
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.50033549G>C, NW_003571045.1:g.192440G>C, NW_017363816.1:g.75175G>C, NR_160275.1:n.676G>C, NM_001005513.1:c.676G>C

Select item 146599909916.

rs1465999099 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 11:50033756 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033755:AA:A
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0.000071/1 (ALFA)
-=0.000043/6 (GnomAD)
-=0.000098/26 (TOPMED)
-=0.000546/1 (Korea1K)
HGVS:: NC_000011.10:g.50033757del, NW_003571045.1:g.192648del, NW_017363816.1:g.75383del, NR_160275.1:n.884del, NM_001005513.1:c.884del

Select item 146577739317.

rs1465777393 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:50032893 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50032892:T:C
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000011.10:g.50032893T>C, NW_003571045.1:g.191784T>C, NW_017363816.1:g.74519T>C, NR_160275.1:n.20T>C, NM_001005513.1:c.20T>C

Select item 146112953818.

rs1461129538 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>-,AA [Show Flanks]
Chromosome:: 11:50033741 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033740:AAAAA:AAAA,NC_000011.10:50033740:AAAAA:AAAAAA
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: AAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.50033745del, NC_000011.10:g.50033745dup, NW_003571045.1:g.192636del, NW_003571045.1:g.192636dup, NW_017363816.1:g.75371del, NW_017363816.1:g.75371dup, NR_160275.1:n.872del, NR_160275.1:n.872dup, NM_001005513.1:c.872del, NM_001005513.1:c.872dup

Select item 146020298519.

rs1460202985 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:50033522 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033521:T:C
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000029/4 (GnomAD)
HGVS:: NC_000011.10:g.50033522T>C, NW_003571045.1:g.192413T>C, NW_017363816.1:g.75148T>C, NR_160275.1:n.649T>C, NM_001005513.1:c.649T>C

Select item 145879275220.

rs1458792752 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:50033438 (GRCh38)
11:-1 (GRCh37)
Canonical SPDI:: NC_000011.10:50033437:A:G
Gene:: OR4C45 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.002562/36 (ALFA)
G=0.00189/265 (GnomAD)
G=0.003733/988 (TOPMED)
G=0.007339/47 (1000Genomes)
G=0.016916/478 (TOMMO)
G=0.019651/36 (Korea1K)
HGVS:: NC_000011.10:g.50033438A>G, NW_003571045.1:g.192329A>G, NW_017363816.1:g.75064A>G, NR_160275.1:n.565A>G, NM_001005513.1:c.565A>G

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