SNP Links for Nucleotide (Select 336285246) - SNP

Links from Nucleotide

Items: 1 to 20 of 308

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Select item 14906600201.

rs1490660020 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:32457394 (GRCh38)
7:32497006 (GRCh37)
Canonical SPDI:: NC_000007.14:32457393:T:C
Gene:: LOC100130673 (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_000007.14:g.32457394T>C, NC_000007.13:g.32497006T>C, NR_038454.1:n.1101A>G

Select item 14879273922.

rs1487927392 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:32458188 (GRCh38)
7:32497800 (GRCh37)
Canonical SPDI:: NC_000007.14:32458187:G:A
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000029/4 (GnomAD)
A=0.000038/10 (TOPMED)
HGVS:: NC_000007.14:g.32458188G>A, NC_000007.13:g.32497800G>A, NR_038454.1:n.307C>T

Select item 14820440923.

rs1482044092 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 7:32456914 (GRCh38)
7:32496526 (GRCh37)
Canonical SPDI:: NC_000007.14:32456913:T:C,NC_000007.14:32456913:T:G
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.32456914T>C, NC_000007.14:g.32456914T>G, NC_000007.13:g.32496526T>C, NC_000007.13:g.32496526T>G, NR_038454.1:n.1581A>G, NR_038454.1:n.1581A>C

Select item 14818033964.

rs1481803396 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:32457556 (GRCh38)
7:32497168 (GRCh37)
Canonical SPDI:: NC_000007.14:32457555:G:T
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_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_000007.14:g.32457556G>T, NC_000007.13:g.32497168G>T, NR_038454.1:n.939C>A

Select item 14814547065.

rs1481454706 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:32456903 (GRCh38)
7:32496515 (GRCh37)
Canonical SPDI:: NC_000007.14:32456902:A:C
Gene:: LOC100130673 (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)
HGVS:: NC_000007.14:g.32456903A>C, NC_000007.13:g.32496515A>C, NR_038454.1:n.1592T>G

Select item 14810263646.

rs1481026364 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:32457523 (GRCh38)
7:32497135 (GRCh37)
Canonical SPDI:: NC_000007.14:32457522:A:C
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.32457523A>C, NC_000007.13:g.32497135A>C, NR_038454.1:n.972T>G

Select item 14807136847.

rs1480713684 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:32457687 (GRCh38)
7:32497299 (GRCh37)
Canonical SPDI:: NC_000007.14:32457686:C:T
Gene:: LOC100130673 (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=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.32457687C>T, NC_000007.13:g.32497299C>T, NR_038454.1:n.808G>A

Select item 14774318948.

rs1477431894 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 7:32457987 (GRCh38)
7:32497599 (GRCh37)
Canonical SPDI:: NC_000007.14:32457986:A:
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.32457987del, NC_000007.13:g.32497599del, NR_038454.1:n.508del

Select item 14761995809.

rs1476199580 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:32457275 (GRCh38)
7:32496887 (GRCh37)
Canonical SPDI:: NC_000007.14:32457274:C:T
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.32457275C>T, NC_000007.13:g.32496887C>T, NR_038454.1:n.1220G>A

Select item 147462768810.

rs1474627688 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:32457113 (GRCh38)
7:32496725 (GRCh37)
Canonical SPDI:: NC_000007.14:32457112:C:A
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
A=0.000036/5 (GnomAD)
HGVS:: NC_000007.14:g.32457113C>A, NC_000007.13:g.32496725C>A, NR_038454.1:n.1382G>T

Select item 146955373211.

rs1469553732 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:32457924 (GRCh38)
7:32497536 (GRCh37)
Canonical SPDI:: NC_000007.14:32457923:T:G
Gene:: LOC100130673 (Varview)
Functional Consequence:: 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)
HGVS:: NC_000007.14:g.32457924T>G, NC_000007.13:g.32497536T>G, NR_038454.1:n.571A>C

Select item 146854858912.

rs1468548589 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:32458184 (GRCh38)
7:32497796 (GRCh37)
Canonical SPDI:: NC_000007.14:32458183:C:T
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.32458184C>T, NC_000007.13:g.32497796C>T, NR_038454.1:n.311G>A

Select item 146273708613.

rs1462737086 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:32458050 (GRCh38)
7:32497662 (GRCh37)
Canonical SPDI:: NC_000007.14:32458049:T:C
Gene:: LOC100130673 (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_000007.14:g.32458050T>C, NC_000007.13:g.32497662T>C, NR_038454.1:n.445A>G

Select item 146260410414.

rs1462604104 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:32457753 (GRCh38)
7:32497365 (GRCh37)
Canonical SPDI:: NC_000007.14:32457752:G:A
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.32457753G>A, NC_000007.13:g.32497365G>A, NR_038454.1:n.742C>T

Select item 146150941515.

rs1461509415 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 7:32457064 (GRCh38)
7:32496676 (GRCh37)
Canonical SPDI:: NC_000007.14:32457063:T:C,NC_000007.14:32457063:T:G
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.32457064T>C, NC_000007.14:g.32457064T>G, NC_000007.13:g.32496676T>C, NC_000007.13:g.32496676T>G, NR_038454.1:n.1431A>G, NR_038454.1:n.1431A>C

Select item 146137351616.

rs1461373516 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:32458224 (GRCh38)
7:32497836 (GRCh37)
Canonical SPDI:: NC_000007.14:32458223:C:T
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.32458224C>T, NC_000007.13:g.32497836C>T, NR_038454.1:n.271G>A

Select item 146015779717.

rs1460157797 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 7:32457576 (GRCh38)
7:32497188 (GRCh37)
Canonical SPDI:: NC_000007.14:32457575:G:A,NC_000007.14:32457575:G:T
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.32457576G>A, NC_000007.14:g.32457576G>T, NC_000007.13:g.32497188G>A, NC_000007.13:g.32497188G>T, NR_038454.1:n.919C>T, NR_038454.1:n.919C>A

Select item 145622621918.

rs1456226219 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:32457615 (GRCh38)
7:32497227 (GRCh37)
Canonical SPDI:: NC_000007.14:32457614:T:C
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.32457615T>C, NC_000007.13:g.32497227T>C, NR_038454.1:n.880A>G

Select item 145528209119.

rs1455282091 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:32457707 (GRCh38)
7:32497319 (GRCh37)
Canonical SPDI:: NC_000007.14:32457706:C:A
Gene:: LOC100130673 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.32457707C>A, NC_000007.13:g.32497319C>A, NR_038454.1:n.788G>T

Select item 145483832420.

rs1454838324 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:32458252 (GRCh38)
7:32497864 (GRCh37)
Canonical SPDI:: NC_000007.14:32458251:G:A
Gene:: LOC100130673 (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=0.00046/8 (TOMMO)
HGVS:: NC_000007.14:g.32458252G>A, NC_000007.13:g.32497864G>A, NR_038454.1:n.243C>T

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