SNP Links for Gene (Select 101928985) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 20 of 1129

<< First< Prev

Page of 57

Next >Last >>

Select item 14905165591.

rs1490516559 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:115735241 (GRCh38)
11:115605959 (GRCh37)
Canonical SPDI:: NC_000011.10:115735240:G:T
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.115735241G>T, NC_000011.9:g.115605959G>T

Select item 14897539132.

rs1489753913 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:115732733 (GRCh38)
11:115603451 (GRCh37)
Canonical SPDI:: NC_000011.10:115732732:T:A
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.115732733T>A, NC_000011.9:g.115603451T>A, NR_135066.2:n.1667A>T, NR_135066.1:n.1667A>T

Select item 14896794353.

rs1489679435 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:115731648 (GRCh38)
11:115602366 (GRCh37)
Canonical SPDI:: NC_000011.10:115731647:G:T
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: downstream_transcript_variant,intron_variant,500B_downstream_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_000011.10:g.115731648G>T, NC_000011.9:g.115602366G>T

Select item 14896326084.

rs1489632608 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 11:115734167 (GRCh38)
11:115604885 (GRCh37)
Canonical SPDI:: NC_000011.10:115734166:A:C,NC_000011.10:115734166:A:G
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.115734167A>C, NC_000011.10:g.115734167A>G, NC_000011.9:g.115604885A>C, NC_000011.9:g.115604885A>G, NR_135066.2:n.596T>G, NR_135066.2:n.596T>C, NR_135066.1:n.596T>G, NR_135066.1:n.596T>C

Select item 14889330465.

rs1488933046 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:115735962 (GRCh38)
11:115606680 (GRCh37)
Canonical SPDI:: NC_000011.10:115735961:G:A
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000224/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000223/1 (Estonian)
HGVS:: NC_000011.10:g.115735962G>A, NC_000011.9:g.115606680G>A

Select item 14883449816.

rs1488344981 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:115736088 (GRCh38)
11:115606806 (GRCh37)
Canonical SPDI:: NC_000011.10:115736087:G:A
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.115736088G>A, NC_000011.9:g.115606806G>A

Select item 14871909717.

rs1487190971 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:115733128 (GRCh38)
11:115603846 (GRCh37)
Canonical SPDI:: NC_000011.10:115733127:C:G
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000011.10:g.115733128C>G, NC_000011.9:g.115603846C>G, NR_135066.2:n.1272G>C, NR_135066.1:n.1272G>C

Select item 14864014328.

rs1486401432 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:115732670 (GRCh38)
11:115603388 (GRCh37)
Canonical SPDI:: NC_000011.10:115732669:G:A,NC_000011.10:115732669:G:T
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.115732670G>A, NC_000011.10:g.115732670G>T, NC_000011.9:g.115603388G>A, NC_000011.9:g.115603388G>T, NR_135066.2:n.1730C>T, NR_135066.2:n.1730C>A, NR_135066.1:n.1730C>T, NR_135066.1:n.1730C>A

Select item 14848772689.

rs1484877268 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:115734078 (GRCh38)
11:115604796 (GRCh37)
Canonical SPDI:: NC_000011.10:115734077:T:G
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.115734078T>G, NC_000011.9:g.115604796T>G, NR_135066.2:n.685A>C, NR_135066.1:n.685A>C

Select item 148428336110.

rs1484283361 has merged into rs1194497997 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTTTTTT>-,GTTTTTTGTTTTTT [Show Flanks]
Chromosome:: 11:115735326 (GRCh38)
11:115606044 (GRCh37)
Canonical SPDI:: NC_000011.10:115735305:TTTTTTGTTTTTTGTTTTTTGTTTTTT:TTTTTTGTTTTTTGTTTTTT,NC_000011.10:115735305:TTTTTTGTTTTTTGTTTTTTGTTTTTT:TTTTTTGTTTTTTGTTTTTTGTTTTTTGTTTTTT
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTGTTTTTTGTTTTTTGTTTTTTGTTTTTT=0./0 (ALFA)
HGVS:: NC_000011.10:g.115735312GTTTTTT[2], NC_000011.10:g.115735312GTTTTTT[4], NC_000011.9:g.115606030GTTTTTT[2], NC_000011.9:g.115606030GTTTTTT[4]

Select item 148338209711.

rs1483382097 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:115735800 (GRCh38)
11:115606518 (GRCh37)
Canonical SPDI:: NC_000011.10:115735799:A:G
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_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_000011.10:g.115735800A>G, NC_000011.9:g.115606518A>G

Select item 148264787812.

rs1482647878 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:115735676 (GRCh38)
11:115606394 (GRCh37)
Canonical SPDI:: NC_000011.10:115735675:G:T
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000011.10:g.115735676G>T, NC_000011.9:g.115606394G>T

Select item 148125152913.

rs1481251529 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:115735829 (GRCh38)
11:115606547 (GRCh37)
Canonical SPDI:: NC_000011.10:115735828:C:T
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_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_000011.10:g.115735829C>T, NC_000011.9:g.115606547C>T

Select item 148114934114.

rs1481149341 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:115733951 (GRCh38)
11:115604669 (GRCh37)
Canonical SPDI:: NC_000011.10:115733950:G:A
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.115733951G>A, NC_000011.9:g.115604669G>A, NR_135066.2:n.812C>T, NR_135066.1:n.812C>T

Select item 148092262415.

rs1480922624 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:115735012 (GRCh38)
11:115605730 (GRCh37)
Canonical SPDI:: NC_000011.10:115735011:T:A
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000029/4 (GnomAD)
HGVS:: NC_000011.10:g.115735012T>A, NC_000011.9:g.115605730T>A

Select item 148075185516.

rs1480751855 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:115732880 (GRCh38)
11:115603598 (GRCh37)
Canonical SPDI:: NC_000011.10:115732879:A:G
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,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)
G=0.000342/1 (KOREAN)
HGVS:: NC_000011.10:g.115732880A>G, NC_000011.9:g.115603598A>G, NR_135066.2:n.1520T>C, NR_135066.1:n.1520T>C

Select item 148012762817.

rs1480127628 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:115734859 (GRCh38)
11:115605577 (GRCh37)
Canonical SPDI:: NC_000011.10:115734858:G:T
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_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_000011.10:g.115734859G>T, NC_000011.9:g.115605577G>T

Select item 147980924318.

rs1479809243 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 11:115733425 (GRCh38)
11:115604143 (GRCh37)
Canonical SPDI:: NC_000011.10:115733424:A:C,NC_000011.10:115733424:A:T
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.115733425A>C, NC_000011.10:g.115733425A>T, NC_000011.9:g.115604143A>C, NC_000011.9:g.115604143A>T

Select item 147917541319.

rs1479175413 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:115731692 (GRCh38)
11:115602410 (GRCh37)
Canonical SPDI:: NC_000011.10:115731691:T:A
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000224/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000223/1 (Estonian)
HGVS:: NC_000011.10:g.115731692T>A, NC_000011.9:g.115602410T>A

Select item 147840003520.

rs1478400035 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:115734404 (GRCh38)
11:115605122 (GRCh37)
Canonical SPDI:: NC_000011.10:115734403:G:A
Gene:: LOC101928985 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.115734404G>A, NC_000011.9:g.115605122G>A, NR_135066.2:n.359C>T, NR_135066.1:n.359C>T