SNP Links for Nucleotide (Select 337756445) - SNP

Links from Nucleotide

Items: 1 to 20 of 473

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Select item 14904324541.

rs1490432454 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:69068465 (GRCh38)
8:69980700 (GRCh37)
Canonical SPDI:: NC_000008.11:69068464:C:T
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
T=0.000026/7 (TOPMED)
HGVS:: NC_000008.11:g.69068465C>T, NC_000008.10:g.69980700C>T, NR_039986.1:n.278G>A

Select item 14900443492.

rs1490044349 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:69104181 (GRCh38)
8:70016416 (GRCh37)
Canonical SPDI:: NC_000008.11:69104180:G:A
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_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_000008.11:g.69104181G>A, NC_000008.10:g.70016416G>A, NR_039986.1:n.10C>T

Select item 14869467013.

rs1486946701 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:68912022 (GRCh38)
8:69824257 (GRCh37)
Canonical SPDI:: NC_000008.11:68912021:A:G
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000008.11:g.68912022A>G, NC_000008.10:g.69824257A>G, NR_039986.1:n.2148T>C

Select item 14868310154.

rs1486831015 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:68913408 (GRCh38)
8:69825643 (GRCh37)
Canonical SPDI:: NC_000008.11:68913407:G:A
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.0002/1 (ALFA)
A=0.0002/1 (Estonian)
HGVS:: NC_000008.11:g.68913408G>A, NC_000008.10:g.69825643G>A, NR_039986.1:n.762C>T

Select item 14865092995.

rs1486509299 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:68913162 (GRCh38)
8:69825397 (GRCh37)
Canonical SPDI:: NC_000008.11:68913161:G:A
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_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_000008.11:g.68913162G>A, NC_000008.10:g.69825397G>A, NR_039986.1:n.1008C>T

Select item 14855233586.

rs1485523358 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:69068459 (GRCh38)
8:69980694 (GRCh37)
Canonical SPDI:: NC_000008.11:69068458:G:A
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000008.11:g.69068459G>A, NC_000008.10:g.69980694G>A, NR_039986.1:n.284C>T

Select item 14841568657.

rs1484156865 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:68912606 (GRCh38)
8:69824841 (GRCh37)
Canonical SPDI:: NC_000008.11:68912605:A:G
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.68912606A>G, NC_000008.10:g.69824841A>G, NR_039986.1:n.1564T>C

Select item 14836951948.

rs1483695194 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:68911982 (GRCh38)
8:69824217 (GRCh37)
Canonical SPDI:: NC_000008.11:68911981:G:A
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.68911982G>A, NC_000008.10:g.69824217G>A, NR_039986.1:n.2188C>T

Select item 14835661639.

rs1483566163 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:68924398 (GRCh38)
8:69836633 (GRCh37)
Canonical SPDI:: NC_000008.11:68924397:G:A
Gene:: LINC01592 (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_000008.11:g.68924398G>A, NC_000008.10:g.69836633G>A, NR_039986.1:n.618C>T

Select item 148286526710.

rs1482865267 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 8:69104017 (GRCh38)
8:70016252 (GRCh37)
Canonical SPDI:: NC_000008.11:69104015:AGA:A
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.69104017_69104018del, NC_000008.10:g.70016252_70016253del, NR_039986.1:n.174_175del

Select item 148025720511.

rs1480257205 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:68924387 (GRCh38)
8:69836622 (GRCh37)
Canonical SPDI:: NC_000008.11:68924386:C:T
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.00003/8 (TOPMED)
HGVS:: NC_000008.11:g.68924387C>T, NC_000008.10:g.69836622C>T, NR_039986.1:n.629G>A

Select item 147982683312.

rs1479826833 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 8:68954080 (GRCh38)
8:69866315 (GRCh37)
Canonical SPDI:: NC_000008.11:68954078:TAT:T
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.68954080_68954081del, NC_000008.10:g.69866315_69866316del, NR_039986.1:n.498_499del

Select item 147892217313.

rs1478922173 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:68912197 (GRCh38)
8:69824432 (GRCh37)
Canonical SPDI:: NC_000008.11:68912196:A:G
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.68912197A>G, NC_000008.10:g.69824432A>G, NR_039986.1:n.1973T>C

Select item 147767857114.

rs1477678571 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 8:68954106 (GRCh38)
8:69866341 (GRCh37)
Canonical SPDI:: NC_000008.11:68954105:C:A
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.68954106C>A, NC_000008.10:g.69866341C>A, NR_039986.1:n.472G>T

Select item 147476264615.

rs1474762646 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:68912157 (GRCh38)
8:69824392 (GRCh37)
Canonical SPDI:: NC_000008.11:68912156:T:C
Gene:: LINC01592 (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_000008.11:g.68912157T>C, NC_000008.10:g.69824392T>C, NR_039986.1:n.2013A>G

Select item 147460173816.

rs1474601738 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 8:68912321 (GRCh38)
8:69824556 (GRCh37)
Canonical SPDI:: NC_000008.11:68912320:G:C,NC_000008.11:68912320:G:T
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000008.11:g.68912321G>C, NC_000008.11:g.68912321G>T, NC_000008.10:g.69824556G>C, NC_000008.10:g.69824556G>T, NR_039986.1:n.1849C>G, NR_039986.1:n.1849C>A

Select item 147427526217.

rs1474275262 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 8:68911803 (GRCh38)
8:69824038 (GRCh37)
Canonical SPDI:: NC_000008.11:68911802:C:
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.68911803del, NC_000008.10:g.69824038del, NR_039986.1:n.2367del

Select item 147404923518.

rs1474049235 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:68913415 (GRCh38)
8:69825650 (GRCh37)
Canonical SPDI:: NC_000008.11:68913414:G:A
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.0002/1 (ALFA)
A=0.0002/1 (Estonian)
HGVS:: NC_000008.11:g.68913415G>A, NC_000008.10:g.69825650G>A, NR_039986.1:n.755C>T

Select item 147359790219.

rs1473597902 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 8:68912542 (GRCh38)
8:69824777 (GRCh37)
Canonical SPDI:: NC_000008.11:68912541:C:A,NC_000008.11:68912541:C:T
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000021/3 (GnomAD)
HGVS:: NC_000008.11:g.68912542C>A, NC_000008.11:g.68912542C>T, NC_000008.10:g.69824777C>A, NC_000008.10:g.69824777C>T, NR_039986.1:n.1628G>T, NR_039986.1:n.1628G>A

Select item 147355726020.

rs1473557260 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:69068332 (GRCh38)
8:69980567 (GRCh37)
Canonical SPDI:: NC_000008.11:69068331:G:A
Gene:: LINC01592 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000093/13 (GnomAD)
A=0.000094/25 (TOPMED)
HGVS:: NC_000008.11:g.69068332G>A, NC_000008.10:g.69980567G>A, NR_039986.1:n.411C>T

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