SNP Links for Nucleotide (Select 565324256) - SNP

Links from Nucleotide

Items: 1 to 20 of 273

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Select item 14879690121.

rs1487969012 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 13:62004456 (GRCh38)
13:62578589 (GRCh37)
Canonical SPDI:: NC_000013.11:62004455:C:A
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000013.11:g.62004456C>A, NC_000013.10:g.62578589C>A, NR_046995.1:n.345G>T

Select item 14846406722.

rs1484640672 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:62029267 (GRCh38)
13:62603400 (GRCh37)
Canonical SPDI:: NC_000013.11:62029266:A:G
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000013.11:g.62029267A>G, NC_000013.10:g.62603400A>G, NR_046995.1:n.282T>C

Select item 14834714823.

rs1483471482 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 13:62003918 (GRCh38)
13:62578051 (GRCh37)
Canonical SPDI:: NC_000013.11:62003917:A:C
Gene:: LINC00358 (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_000013.11:g.62003918A>C, NC_000013.10:g.62578051A>C, NR_046995.1:n.883T>G

Select item 14829656104.

rs1482965610 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 13:62029536 (GRCh38)
13:62603669 (GRCh37)
Canonical SPDI:: NC_000013.11:62029535:T:A
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000013.11:g.62029536T>A, NC_000013.10:g.62603669T>A, NR_046995.1:n.13A>T

Select item 14819546405.

rs1481954640 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 13:62004085 (GRCh38)
13:62578218 (GRCh37)
Canonical SPDI:: NC_000013.11:62004084:G:A,NC_000013.11:62004084:G:T
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.62004085G>A, NC_000013.11:g.62004085G>T, NC_000013.10:g.62578218G>A, NC_000013.10:g.62578218G>T, NR_046995.1:n.716C>T, NR_046995.1:n.716C>A

Select item 14750609916.

rs1475060991 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:62029423 (GRCh38)
13:62603556 (GRCh37)
Canonical SPDI:: NC_000013.11:62029422:C:T
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
HGVS:: NC_000013.11:g.62029423C>T, NC_000013.10:g.62603556C>T, NR_046995.1:n.126G>A

Select item 14728919057.

rs1472891905 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:62003647 (GRCh38)
13:62577780 (GRCh37)
Canonical SPDI:: NC_000013.11:62003646:A:G
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000013.11:g.62003647A>G, NC_000013.10:g.62577780A>G, NR_046995.1:n.1154T>C

Select item 14723813518.

rs1472381351 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 13:62003557 (GRCh38)
13:62577690 (GRCh37)
Canonical SPDI:: NC_000013.11:62003556:TTTT:TTT
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.62003560del, NC_000013.10:g.62577693del, NR_046995.1:n.1244del

Select item 14715430679.

rs1471543067 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:62003955 (GRCh38)
13:62578088 (GRCh37)
Canonical SPDI:: NC_000013.11:62003954:T:C
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.62003955T>C, NC_000013.10:g.62578088T>C, NR_046995.1:n.846A>G

Select item 147152122910.

rs1471521229 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:62004426 (GRCh38)
13:62578559 (GRCh37)
Canonical SPDI:: NC_000013.11:62004425:A:G
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.62004426A>G, NC_000013.10:g.62578559A>G, NR_046995.1:n.375T>C

Select item 147107687511.

rs1471076875 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:62003641 (GRCh38)
13:62577774 (GRCh37)
Canonical SPDI:: NC_000013.11:62003640:G:A
Gene:: LINC00358 (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_000013.11:g.62003641G>A, NC_000013.10:g.62577774G>A, NR_046995.1:n.1160C>T

Select item 147088340512.

rs1470883405 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 13:62004411 (GRCh38)
13:62578544 (GRCh37)
Canonical SPDI:: NC_000013.11:62004410:C:A
Gene:: LINC00358 (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=0.000023/6 (TOPMED)
HGVS:: NC_000013.11:g.62004411C>A, NC_000013.10:g.62578544C>A, NR_046995.1:n.390G>T

Select item 146659178813.

rs1466591788 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 13:62003584 (GRCh38)
13:62577717 (GRCh37)
Canonical SPDI:: NC_000013.11:62003583:T:G
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.62003584T>G, NC_000013.10:g.62577717T>G, NR_046995.1:n.1217A>C

Select item 146402993014.

rs1464029930 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:62003557 (GRCh38)
13:62577690 (GRCh37)
Canonical SPDI:: NC_000013.11:62003556:T:C
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000042/11 (TOPMED)
C=0.00005/7 (GnomAD)
HGVS:: NC_000013.11:g.62003557T>C, NC_000013.10:g.62577690T>C, NR_046995.1:n.1244A>G

Select item 146210346015.

rs1462103460 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 13:62004451 (GRCh38)
13:62578584 (GRCh37)
Canonical SPDI:: NC_000013.11:62004450:A:T
Gene:: LINC00358 (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_000013.11:g.62004451A>T, NC_000013.10:g.62578584A>T, NR_046995.1:n.350T>A

Select item 145983029216.

rs1459830292 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:62004226 (GRCh38)
13:62578359 (GRCh37)
Canonical SPDI:: NC_000013.11:62004225:C:T
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.62004226C>T, NC_000013.10:g.62578359C>T, NR_046995.1:n.575G>A

Select item 145779555717.

rs1457795557 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:62004361 (GRCh38)
13:62578494 (GRCh37)
Canonical SPDI:: NC_000013.11:62004360:G:A
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.62004361G>A, NC_000013.10:g.62578494G>A, NR_046995.1:n.440C>T

Select item 145460881318.

rs1454608813 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:62004116 (GRCh38)
13:62578249 (GRCh37)
Canonical SPDI:: NC_000013.11:62004115:T:C
Gene:: LINC00358 (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_000013.11:g.62004116T>C, NC_000013.10:g.62578249T>C, NR_046995.1:n.685A>G

Select item 145355953919.

rs1453559539 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 13:62004498 (GRCh38)
13:62578631 (GRCh37)
Canonical SPDI:: NC_000013.11:62004497:A:T
Gene:: LINC00358 (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_000013.11:g.62004498A>T, NC_000013.10:g.62578631A>T, NR_046995.1:n.303T>A

Select item 145077136920.

rs1450771369 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 13:62029370 (GRCh38)
13:62603503 (GRCh37)
Canonical SPDI:: NC_000013.11:62029369:C:G
Gene:: LINC00358 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
G=0.000029/4 (GnomAD)
HGVS:: NC_000013.11:g.62029370C>G, NC_000013.10:g.62603503C>G, NR_046995.1:n.179G>C

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Links from Nucleotide

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