SNP Links for Nucleotide (Select 565324250) - SNP

Links from Nucleotide

Items: 1 to 20 of 277

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Select item 14779304651.

rs1477930465 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:99805936 (GRCh38)
9:102568218 (GRCh37)
Canonical SPDI:: NC_000009.12:99805935:T:A
Gene:: LOC101928438 (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_000009.12:g.99805936T>A, NC_000009.11:g.102568218T>A, NR_109802.1:n.125A>T

Select item 14769202452.

rs1476920245 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:99586524 (GRCh38)
9:102348806 (GRCh37)
Canonical SPDI:: NC_000009.12:99586523:C:A
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000009.12:g.99586524C>A, NC_000009.11:g.102348806C>A, NR_109802.1:n.806G>T

Select item 14709821933.

rs1470982193 [Homo sapiens]

Variant type:: SNV:
Alleles:: T>C
Chromosome:: no mapping
Canonical SPDI:

Select item 14708499174.

rs1470849917 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:99585793 (GRCh38)
9:102348075 (GRCh37)
Canonical SPDI:: NC_000009.12:99585792:C:A,NC_000009.12:99585792:C:T
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.99585793C>A, NC_000009.12:g.99585793C>T, NC_000009.11:g.102348075C>A, NC_000009.11:g.102348075C>T, NR_109802.1:n.1537G>T, NR_109802.1:n.1537G>A

Select item 14695278235.

rs1469527823 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:99586411 (GRCh38)
9:102348693 (GRCh37)
Canonical SPDI:: NC_000009.12:99586410:C:T
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.99586411C>T, NC_000009.11:g.102348693C>T, NR_109802.1:n.919G>A

Select item 14662361916.

rs1466236191 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:99588449 (GRCh38)
9:102350731 (GRCh37)
Canonical SPDI:: NC_000009.12:99588448:T:A
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000009.12:g.99588449T>A, NC_000009.11:g.102350731T>A, NR_109802.1:n.555A>T

Select item 14644213517.

rs1464421351 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:99586504 (GRCh38)
9:102348786 (GRCh37)
Canonical SPDI:: NC_000009.12:99586503:G:C
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000054/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
C=0.000223/1 (Estonian)
HGVS:: NC_000009.12:g.99586504G>C, NC_000009.11:g.102348786G>C, NR_109802.1:n.826C>G

Select item 14605347698.

rs1460534769 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 9:99586963 (GRCh38)
9:102349245 (GRCh37)
Canonical SPDI:: NC_000009.12:99586962:TTTT:TTT
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTT=0./0 (ALFA)
HGVS:: NC_000009.12:g.99586966del, NC_000009.11:g.102349248del, NR_109802.1:n.601del

Select item 14598270699.

rs1459827069 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:99586263 (GRCh38)
9:102348545 (GRCh37)
Canonical SPDI:: NC_000009.12:99586262:T:C
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000009.12:g.99586263T>C, NC_000009.11:g.102348545T>C, NR_109802.1:n.1067A>G

Select item 145919489610.

rs1459194896 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:99805986 (GRCh38)
9:102568268 (GRCh37)
Canonical SPDI:: NC_000009.12:99805985:T:C
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000036/5 (GnomAD)
C=0.000072/19 (TOPMED)
HGVS:: NC_000009.12:g.99805986T>C, NC_000009.11:g.102568268T>C, NR_109802.1:n.75A>G

Select item 144588622011.

rs1445886220 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:99585979 (GRCh38)
9:102348261 (GRCh37)
Canonical SPDI:: NC_000009.12:99585978:G:A
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.99585979G>A, NC_000009.11:g.102348261G>A, NR_109802.1:n.1351C>T

Select item 144473281512.

rs1444732815 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:99586151 (GRCh38)
9:102348433 (GRCh37)
Canonical SPDI:: NC_000009.12:99586150:G:T
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000034/9 (TOPMED)
HGVS:: NC_000009.12:g.99586151G>T, NC_000009.11:g.102348433G>T, NR_109802.1:n.1179C>A

Select item 144152986913.

rs1441529869 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>T
Chromosome:: no mapping
Canonical SPDI:

Select item 144126946514.

rs1441269465 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:99718273 (GRCh38)
9:102480555 (GRCh37)
Canonical SPDI:: NC_000009.12:99718272:G:T
Gene:: LOC101928438 (Varview), LOC124902234 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.99718273G>T, NC_000009.11:g.102480555G>T, NR_109802.1:n.205C>A

Select item 143847069315.

rs1438470693 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:99586429 (GRCh38)
9:102348711 (GRCh37)
Canonical SPDI:: NC_000009.12:99586428:G:A
Gene:: LOC101928438 (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_000009.12:g.99586429G>A, NC_000009.11:g.102348711G>A, NR_109802.1:n.901C>T

Select item 143784452516.

rs1437844525 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:99588503 (GRCh38)
9:102350785 (GRCh37)
Canonical SPDI:: NC_000009.12:99588502:G:T
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_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_000009.12:g.99588503G>T, NC_000009.11:g.102350785G>T, NR_109802.1:n.501C>A

Select item 143653451517.

rs1436534515 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:99586589 (GRCh38)
9:102348871 (GRCh37)
Canonical SPDI:: NC_000009.12:99586588:T:C
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000224/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000223/1 (Estonian)
HGVS:: NC_000009.12:g.99586589T>C, NC_000009.11:g.102348871T>C, NR_109802.1:n.741A>G

Select item 143478344018.

rs1434783440 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:99819847 (GRCh38)
9:102582129 (GRCh37)
Canonical SPDI:: NC_000009.12:99819846:C:G
Gene:: LOC101928438 (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=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.99819847C>G, NC_000009.11:g.102582129C>G, NG_028910.1:g.2993C>G, NR_109802.1:n.43G>C

Select item 143312448619.

rs1433124486 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:99586190 (GRCh38)
9:102348472 (GRCh37)
Canonical SPDI:: NC_000009.12:99586189:A:T
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.99586190A>T, NC_000009.11:g.102348472A>T, NR_109802.1:n.1140T>A

Select item 142641199520.

rs1426411995 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:99805899 (GRCh38)
9:102568181 (GRCh37)
Canonical SPDI:: NC_000009.12:99805898:A:G
Gene:: LOC101928438 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.99805899A>G, NC_000009.11:g.102568181A>G, NR_109802.1:n.162T>C

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Links from Nucleotide

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