SNP Links for Nucleotide (Select 343432582) - SNP

Links from Nucleotide

Items: 1 to 20 of 292

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Select item 14892124151.

rs1489212415 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:17052000 (GRCh38)
11:17073547 (GRCh37)
Canonical SPDI:: NC_000011.10:17051999:C:A
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.17052000C>A, NC_000011.9:g.17073547C>A, NR_045002.1:n.115C>A

Select item 14872723112.

rs1487272311 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:17051916 (GRCh38)
11:17073463 (GRCh37)
Canonical SPDI:: NC_000011.10:17051915:A:G
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.17051916A>G, NC_000011.9:g.17073463A>G, NR_045002.1:n.31A>G

Select item 14867030923.

rs1486703092 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:17052353 (GRCh38)
11:17073900 (GRCh37)
Canonical SPDI:: NC_000011.10:17052352:A:G
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.17052353A>G, NC_000011.9:g.17073900A>G, NR_045002.1:n.468A>G

Select item 14844909374.

rs1484490937 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 11:17052191 (GRCh38)
11:17073738 (GRCh37)
Canonical SPDI:: NC_000011.10:17052190:T:
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
-=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.17052191del, NC_000011.9:g.17073738del, NR_045002.1:n.306del

Select item 14838957985.

rs1483895798 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:17052451 (GRCh38)
11:17073998 (GRCh37)
Canonical SPDI:: NC_000011.10:17052450:T:C
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.0007/6 (ALFA)
HGVS:: NC_000011.10:g.17052451T>C, NC_000011.9:g.17073998T>C, NR_045002.1:n.566T>C

Select item 14836250436.

rs1483625043 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:17052490 (GRCh38)
11:17074037 (GRCh37)
Canonical SPDI:: NC_000011.10:17052489:G:C
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_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.17052490G>C, NC_000011.9:g.17074037G>C, NR_045002.1:n.605G>C

Select item 14831525167.

rs1483152516 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:17052085 (GRCh38)
11:17073632 (GRCh37)
Canonical SPDI:: NC_000011.10:17052084:A:G
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000011.10:g.17052085A>G, NC_000011.9:g.17073632A>G, NR_045002.1:n.200A>G

Select item 14825034228.

rs1482503422 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:17052650 (GRCh38)
11:17074197 (GRCh37)
Canonical SPDI:: NC_000011.10:17052649:T:C
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000312/2 (1000Genomes)
HGVS:: NC_000011.10:g.17052650T>C, NC_000011.9:g.17074197T>C, NR_045002.1:n.765T>C

Select item 14821695749.

rs1482169574 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:17052383 (GRCh38)
11:17073930 (GRCh37)
Canonical SPDI:: NC_000011.10:17052382:G:A
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000011.10:g.17052383G>A, NC_000011.9:g.17073930G>A, NR_045002.1:n.498G>A

Select item 147374696810.

rs1473746968 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:17052426 (GRCh38)
11:17073973 (GRCh37)
Canonical SPDI:: NC_000011.10:17052425:T:C
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_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.17052426T>C, NC_000011.9:g.17073973T>C, NR_045002.1:n.541T>C

Select item 147349342411.

rs1473493424 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:17052342 (GRCh38)
11:17073889 (GRCh37)
Canonical SPDI:: NC_000011.10:17052341:G:A
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000011.10:g.17052342G>A, NC_000011.9:g.17073889G>A, NR_045002.1:n.457G>A

Select item 147332249212.

rs1473322492 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:17051995 (GRCh38)
11:17073542 (GRCh37)
Canonical SPDI:: NC_000011.10:17051994:G:C
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.17051995G>C, NC_000011.9:g.17073542G>C, NR_045002.1:n.110G>C

Select item 147310123013.

rs1473101230 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:17052398 (GRCh38)
11:17073945 (GRCh37)
Canonical SPDI:: NC_000011.10:17052397:C:T
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.17052398C>T, NC_000011.9:g.17073945C>T, NR_045002.1:n.513C>T

Select item 147245297814.

rs1472452978 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 11:17052019 (GRCh38)
11:17073566 (GRCh37)
Canonical SPDI:: NC_000011.10:17052018:CCC:CC
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: -=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.17052021del, NC_000011.9:g.17073568del, NR_045002.1:n.136del

Select item 147064264815.

rs1470642648 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 11:17052632 (GRCh38)
11:17074179 (GRCh37)
Canonical SPDI:: NC_000011.10:17052631:C:A,NC_000011.10:17052631:C:G,NC_000011.10:17052631:C:T
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000011.10:g.17052632C>A, NC_000011.10:g.17052632C>G, NC_000011.10:g.17052632C>T, NC_000011.9:g.17074179C>A, NC_000011.9:g.17074179C>G, NC_000011.9:g.17074179C>T, NR_045002.1:n.747C>A, NR_045002.1:n.747C>G, NR_045002.1:n.747C>T

Select item 146838181016.

rs1468381810 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 11:17052334 (GRCh38)
11:17073881 (GRCh37)
Canonical SPDI:: NC_000011.10:17052333:T:C,NC_000011.10:17052333:T:G
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.17052334T>C, NC_000011.10:g.17052334T>G, NC_000011.9:g.17073881T>C, NC_000011.9:g.17073881T>G, NR_045002.1:n.449T>C, NR_045002.1:n.449T>G

Select item 146538051217.

rs1465380512 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:17052783 (GRCh38)
11:17074330 (GRCh37)
Canonical SPDI:: NC_000011.10:17052782:G:T
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.17052783G>T, NC_000011.9:g.17074330G>T, NR_045002.1:n.898G>T

Select item 146537521718.

rs1465375217 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:17052267 (GRCh38)
11:17073814 (GRCh37)
Canonical SPDI:: NC_000011.10:17052266:C:G,NC_000011.10:17052266:C:T
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.25974/40 (SGDP_PRJ)
HGVS:: NC_000011.10:g.17052267C>G, NC_000011.10:g.17052267C>T, NC_000011.9:g.17073814C>G, NC_000011.9:g.17073814C>T, NR_045002.1:n.382C>G, NR_045002.1:n.382C>T

Select item 146523660819.

rs1465236608 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:17052307 (GRCh38)
11:17073854 (GRCh37)
Canonical SPDI:: NC_000011.10:17052306:A:G
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.17052307A>G, NC_000011.9:g.17073854A>G, NR_045002.1:n.422A>G

Select item 145479303920.

rs1454793039 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:17053028 (GRCh38)
11:17074575 (GRCh37)
Canonical SPDI:: NC_000011.10:17053027:G:A
Gene:: OR7E14P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.17053028G>A, NC_000011.9:g.17074575G>A, NR_045002.1:n.1143G>A

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