SNP Links for Nucleotide (Select 673536545) - SNP

Links from Nucleotide

Items: 1 to 20 of 95

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Select item 14840176061.

rs1484017606 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:64368414 (GRCh38)
8:65280971 (GRCh37)
Canonical SPDI:: NC_000008.11:64368413:G:C
Gene:: LINC01414 (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)
C=0.000035/1 (TOMMO)
HGVS:: NC_000008.11:g.64368414G>C, NC_000008.10:g.65280971G>C, NR_125826.1:n.145C>G

Select item 14732774262.

rs1473277426 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 8:64368490 (GRCh38)
8:65281047 (GRCh37)
Canonical SPDI:: NC_000008.11:64368489:C:A
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000008.11:g.64368490C>A, NC_000008.10:g.65281047C>A, NR_125826.1:n.69G>T

Select item 14728441103.

rs1472844110 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:64368399 (GRCh38)
8:65280956 (GRCh37)
Canonical SPDI:: NC_000008.11:64368398:G:T
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000008.11:g.64368399G>T, NC_000008.10:g.65280956G>T, NR_125826.1:n.160C>A

Select item 14682379544.

rs1468237954 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 8:64368521 (GRCh38)
8:65281078 (GRCh37)
Canonical SPDI:: NC_000008.11:64368520:A:C
Gene:: LINC01414 (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_000008.11:g.64368521A>C, NC_000008.10:g.65281078A>C, NR_125826.1:n.38T>G

Select item 14671500915.

rs1467150091 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 8:64167013 (GRCh38)
8:65079570 (GRCh37)
Canonical SPDI:: NC_000008.11:64167012:C:A,NC_000008.11:64167012:C:G
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000008.11:g.64167013C>A, NC_000008.11:g.64167013C>G, NC_000008.10:g.65079570C>A, NC_000008.10:g.65079570C>G, NR_125826.1:n.233G>T, NR_125826.1:n.233G>C

Select item 14577103666.

rs1457710366 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:64133449 (GRCh38)
8:65046006 (GRCh37)
Canonical SPDI:: NC_000008.11:64133448:T:C
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.64133449T>C, NC_000008.10:g.65046006T>C, NR_125826.1:n.409A>G

Select item 14436011597.

rs1443601159 [Homo sapiens]

Variant type:: DELINS
Alleles:: GG>- [Show Flanks]
Chromosome:: 8:63856950 (GRCh38)
8:64769507 (GRCh37)
Canonical SPDI:: NC_000008.11:63856948:GGG:G
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.63856950_63856951del, NC_000008.10:g.64769507_64769508del, NR_125826.1:n.572_573del

Select item 14345337068.

rs1434533706 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:63856979 (GRCh38)
8:64769536 (GRCh37)
Canonical SPDI:: NC_000008.11:63856978:G:A
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000008.11:g.63856979G>A, NC_000008.10:g.64769536G>A, NR_125826.1:n.543C>T

Select item 14272145079.

rs1427214507 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:64167003 (GRCh38)
8:65079560 (GRCh37)
Canonical SPDI:: NC_000008.11:64167002:T:C
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
T=0./0 (SGDP_PRJ)
C=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.64167003T>C, NC_000008.10:g.65079560T>C, NR_125826.1:n.243A>G

Select item 142471866610.

rs1424718666 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:64167027 (GRCh38)
8:65079584 (GRCh37)
Canonical SPDI:: NC_000008.11:64167026:T:C
Gene:: LINC01414 (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_000008.11:g.64167027T>C, NC_000008.10:g.65079584T>C, NR_125826.1:n.219A>G

Select item 141500004911.

rs1415000049 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:63857105 (GRCh38)
8:64769662 (GRCh37)
Canonical SPDI:: NC_000008.11:63857104:G:T
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000015/4 (TOPMED)
T=0.000685/2 (KOREAN)
HGVS:: NC_000008.11:g.63857105G>T, NC_000008.10:g.64769662G>T, NR_125826.1:n.417C>A

Select item 140857285512.

rs1408572855 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 8:64368394 (GRCh38)
8:65280951 (GRCh37)
Canonical SPDI:: NC_000008.11:64368393:A:T
Gene:: LINC01414 (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_000008.11:g.64368394A>T, NC_000008.10:g.65280951A>T, NR_125826.1:n.165T>A

Select item 140514081813.

rs1405140818 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 8:64166980 (GRCh38)
8:65079537 (GRCh37)
Canonical SPDI:: NC_000008.11:64166979:T:A,NC_000008.11:64166979:T:G
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000008.11:g.64166980T>A, NC_000008.11:g.64166980T>G, NC_000008.10:g.65079537T>A, NC_000008.10:g.65079537T>G, NR_125826.1:n.266A>T, NR_125826.1:n.266A>C

Select item 140106125114.

rs1401061251 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>-,TT [Show Flanks]
Chromosome:: 8:64167019 (GRCh38)
8:65079576 (GRCh37)
Canonical SPDI:: NC_000008.11:64167018:TTTT:TTT,NC_000008.11:64167018:TTTT:TTTTT
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTT=0./0 (ALFA)
-=0.000042/11 (TOPMED)
HGVS:: NC_000008.11:g.64167022del, NC_000008.11:g.64167022dup, NC_000008.10:g.65079579del, NC_000008.10:g.65079579dup, NR_125826.1:n.227del, NR_125826.1:n.227dup

Select item 138893402815.

rs1388934028 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 8:64133488 (GRCh38)
8:65046045 (GRCh37)
Canonical SPDI:: NC_000008.11:64133487:C:G
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.64133488C>G, NC_000008.10:g.65046045C>G, NR_125826.1:n.370G>C

Select item 137169459316.

rs1371694593 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:64368376 (GRCh38)
8:65280933 (GRCh37)
Canonical SPDI:: NC_000008.11:64368375:G:A
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.64368376G>A, NC_000008.10:g.65280933G>A, NR_125826.1:n.183C>T

Select item 136921574117.

rs1369215741 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:64151152 (GRCh38)
8:65063709 (GRCh37)
Canonical SPDI:: NC_000008.11:64151151:T:C
Gene:: LINC01414 (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=0.000015/4 (TOPMED)
HGVS:: NC_000008.11:g.64151152T>C, NC_000008.10:g.65063709T>C, NR_125826.1:n.284A>G

Select item 135652305618.

rs1356523056 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 8:63857067 (GRCh38)
8:64769624 (GRCh37)
Canonical SPDI:: NC_000008.11:63857066:G:A,NC_000008.11:63857066:G:C
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000008.11:g.63857067G>A, NC_000008.11:g.63857067G>C, NC_000008.10:g.64769624G>A, NC_000008.10:g.64769624G>C, NR_125826.1:n.455C>T, NR_125826.1:n.455C>G

Select item 134428619219.

rs1344286192 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:63857086 (GRCh38)
8:64769643 (GRCh37)
Canonical SPDI:: NC_000008.11:63857085:C:T
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.63857086C>T, NC_000008.10:g.64769643C>T, NR_125826.1:n.436G>A

Select item 134326161920.

rs1343261619 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 8:64133463 (GRCh38)
8:65046020 (GRCh37)
Canonical SPDI:: NC_000008.11:64133462:C:A
Gene:: LINC01414 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.64133463C>A, NC_000008.10:g.65046020C>A, NR_125826.1:n.395G>T

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