SNP Links for Nucleotide (Select 991820368) - SNP

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Links from Nucleotide

Items: 1 to 20 of 135

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Select item 14601905581.

rs1460190558 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:88077755 (GRCh38)
9:90692670 (GRCh37)
Canonical SPDI:: NC_000009.12:88077754:G:A
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_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_000009.12:g.88077755G>A, NC_000009.11:g.90692670G>A, XM_047424307.1:c.-3069C>T, NR_135137.1:n.146C>T, NR_135138.1:n.146C>T

Select item 14598762222.

rs1459876222 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:88066662 (GRCh38)
9:90681577 (GRCh37)
Canonical SPDI:: NC_000009.12:88066661:T:C
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.88066662T>C, NC_000009.11:g.90681577T>C, XM_047424307.1:c.-2718A>G, NR_135137.1:n.399A>G, NR_135138.1:n.298A>G

Select item 14553695573.

rs1455369557 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:88077848 (GRCh38)
9:90692763 (GRCh37)
Canonical SPDI:: NC_000009.12:88077847:G:A,NC_000009.12:88077847:G:C
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000009.12:g.88077848G>A, NC_000009.12:g.88077848G>C, NC_000009.11:g.90692763G>A, NC_000009.11:g.90692763G>C, XM_047424307.1:c.-3162C>T, XM_047424307.1:c.-3162C>G, NR_135137.1:n.53C>T, NR_135137.1:n.53C>G, NR_135138.1:n.53C>T, NR_135138.1:n.53C>G

Select item 14547614444.

rs1454761444 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:88077420 (GRCh38)
9:90692335 (GRCh37)
Canonical SPDI:: NC_000009.12:88077419:C:G
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,5_prime_UTR_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.88077420C>G, NC_000009.11:g.90692335C>G, XM_047424307.1:c.-2973G>C, NR_135137.1:n.242G>C

Select item 14540483655.

rs1454048365 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:88066731 (GRCh38)
9:90681646 (GRCh37)
Canonical SPDI:: NC_000009.12:88066730:T:C
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000009.12:g.88066731T>C, NC_000009.11:g.90681646T>C, XM_047424307.1:c.-2787A>G, NR_135137.1:n.330A>G, NR_135138.1:n.229A>G

Select item 14448567056.

rs1444856705 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 9:88077471 (GRCh38)
9:90692386 (GRCh37)
Canonical SPDI:: NC_000009.12:88077470:GG:G
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.88077472del, NC_000009.11:g.90692387del, XM_047424307.1:c.-3024del, NR_135137.1:n.191del

Select item 14261465127.

rs1426146512 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:88066562 (GRCh38)
9:90681477 (GRCh37)
Canonical SPDI:: NC_000009.12:88066561:G:C
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_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_000009.12:g.88066562G>C, NC_000009.11:g.90681477G>C, XM_047424307.1:c.-2618C>G, NR_135137.1:n.499C>G, NR_135138.1:n.398C>G

Select item 14177012078.

rs1417701207 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 9:88066546 (GRCh38)
9:90681461 (GRCh37)
Canonical SPDI:: NC_000009.12:88066545:T:G
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.88066546T>G, NC_000009.11:g.90681461T>G, XM_047424307.1:c.-2602A>C, NR_135137.1:n.515A>C, NR_135138.1:n.414A>C

Select item 14145900409.

rs1414590040 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:88066564 (GRCh38)
9:90681479 (GRCh37)
Canonical SPDI:: NC_000009.12:88066563:G:A
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000035/1 (TOMMO)
HGVS:: NC_000009.12:g.88066564G>A, NC_000009.11:g.90681479G>A, XM_047424307.1:c.-2620C>T, NR_135137.1:n.497C>T, NR_135138.1:n.396C>T

Select item 140944596710.

rs1409445967 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:88066617 (GRCh38)
9:90681532 (GRCh37)
Canonical SPDI:: NC_000009.12:88066616:T:C
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.88066617T>C, NC_000009.11:g.90681532T>C, XM_047424307.1:c.-2673A>G, NR_135137.1:n.444A>G, NR_135138.1:n.343A>G

Select item 140835092211.

rs1408350922 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:88077759 (GRCh38)
9:90692674 (GRCh37)
Canonical SPDI:: NC_000009.12:88077758:A:G
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.88077759A>G, NC_000009.11:g.90692674A>G, XM_047424307.1:c.-3073T>C, NR_135137.1:n.142T>C, NR_135138.1:n.142T>C

Select item 140828159912.

rs1408281599 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:88066670 (GRCh38)
9:90681585 (GRCh37)
Canonical SPDI:: NC_000009.12:88066669:G:A
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.88066670G>A, NC_000009.11:g.90681585G>A, XM_047424307.1:c.-2726C>T, NR_135137.1:n.391C>T, NR_135138.1:n.290C>T

Select item 139626847713.

rs1396268477 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:88066586 (GRCh38)
9:90681501 (GRCh37)
Canonical SPDI:: NC_000009.12:88066585:G:A
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000009.12:g.88066586G>A, NC_000009.11:g.90681501G>A, XM_047424307.1:c.-2642C>T, NR_135137.1:n.475C>T, NR_135138.1:n.374C>T

Select item 139218972314.

rs1392189723 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:88066714 (GRCh38)
9:90681629 (GRCh37)
Canonical SPDI:: NC_000009.12:88066713:T:C
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_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_000009.12:g.88066714T>C, NC_000009.11:g.90681629T>C, XM_047424307.1:c.-2770A>G, NR_135137.1:n.347A>G, NR_135138.1:n.246A>G

Select item 138479638715.

rs1384796387 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:88077844 (GRCh38)
9:90692759 (GRCh37)
Canonical SPDI:: NC_000009.12:88077843:G:A
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.88077844G>A, NC_000009.11:g.90692759G>A, XM_047424307.1:c.-3158C>T, NR_135137.1:n.57C>T, NR_135138.1:n.57C>T

Select item 138439072516.

rs1384390725 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:88077897 (GRCh38)
9:90692812 (GRCh37)
Canonical SPDI:: NC_000009.12:88077896:T:C
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_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_000009.12:g.88077897T>C, NC_000009.11:g.90692812T>C, XM_047424307.1:c.-3211A>G, NR_135137.1:n.4A>G, NR_135138.1:n.4A>G

Select item 136988783017.

rs1369887830 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:88066754 (GRCh38)
9:90681669 (GRCh37)
Canonical SPDI:: NC_000009.12:88066753:A:G
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000009.12:g.88066754A>G, NC_000009.11:g.90681669A>G, XM_047424307.1:c.-2810T>C, NR_135137.1:n.307T>C, NR_135138.1:n.206T>C

Select item 136683663018.

rs1366836630 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:88066622 (GRCh38)
9:90681537 (GRCh37)
Canonical SPDI:: NC_000009.12:88066621:C:G
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.88066622C>G, NC_000009.11:g.90681537C>G, XM_047424307.1:c.-2678G>C, NR_135137.1:n.439G>C, NR_135138.1:n.338G>C

Select item 136378068119.

rs1363780681 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:88077733 (GRCh38)
9:90692648 (GRCh37)
Canonical SPDI:: NC_000009.12:88077732:G:A
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000015/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.88077733G>A, NC_000009.11:g.90692648G>A, XM_047424307.1:c.-3047C>T, NR_135137.1:n.168C>T, NR_135138.1:n.168C>T

Select item 136181433620.

rs1361814336 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:88077899 (GRCh38)
9:90692814 (GRCh37)
Canonical SPDI:: NC_000009.12:88077898:C:T
Gene:: LINC03026 (Varview), LOC124902201 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.88077899C>T, NC_000009.11:g.90692814C>T, XM_047424307.1:c.-3213G>A, NR_135137.1:n.2G>A, NR_135138.1:n.2G>A