SNP Links for Nucleotide (Select 323668301) - SNP

Links from Nucleotide

Items: 1 to 20 of 550

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Select item 14908163041.

rs1490816304 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 3:154025802 (GRCh38)
3:153743591 (GRCh37)
Canonical SPDI:: NC_000003.12:154025801:C:A,NC_000003.12:154025801:C:G,NC_000003.12:154025801:C:T
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000003.12:g.154025802C>A, NC_000003.12:g.154025802C>G, NC_000003.12:g.154025802C>T, NC_000003.11:g.153743591C>A, NC_000003.11:g.153743591C>G, NC_000003.11:g.153743591C>T, NR_037901.1:n.1197G>T, NR_037901.1:n.1197G>C, NR_037901.1:n.1197G>A

Select item 14903246892.

rs1490324689 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 3:154026399 (GRCh38)
3:153744188 (GRCh37)
Canonical SPDI:: NC_000003.12:154026397:ACA:A
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000003.12:g.154026399_154026400del, NC_000003.11:g.153744188_153744189del, NR_037901.1:n.600_601del

Select item 14870819473.

rs1487081947 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:154026347 (GRCh38)
3:153744136 (GRCh37)
Canonical SPDI:: NC_000003.12:154026346:A:G
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.0002/1 (ALFA)
G=0.0002/1 (Estonian)
HGVS:: NC_000003.12:g.154026347A>G, NC_000003.11:g.153744136A>G, NR_037901.1:n.652T>C

Select item 14821575394.

rs1482157539 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:154025578 (GRCh38)
3:153743367 (GRCh37)
Canonical SPDI:: NC_000003.12:154025577:T:C
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.154025578T>C, NC_000003.11:g.153743367T>C, NR_037901.1:n.1421A>G

Select item 14817390265.

rs1481739026 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 3:154026529 (GRCh38)
3:153744318 (GRCh37)
Canonical SPDI:: NC_000003.12:154026528:A:C,NC_000003.12:154026528:A:G
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000003.12:g.154026529A>C, NC_000003.12:g.154026529A>G, NC_000003.11:g.153744318A>C, NC_000003.11:g.153744318A>G, NR_037901.1:n.470T>G, NR_037901.1:n.470T>C

Select item 14814004086.

rs1481400408 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:154025958 (GRCh38)
3:153743747 (GRCh37)
Canonical SPDI:: NC_000003.12:154025957:T:C
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.154025958T>C, NC_000003.11:g.153743747T>C, NR_037901.1:n.1041A>G

Select item 14786861537.

rs1478686153 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 3:154025129 (GRCh38)
3:153742918 (GRCh37)
Canonical SPDI:: NC_000003.12:154025128:A:G,NC_000003.12:154025128:A:T
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.001387/21 (ALFA)
G=0.000008/1 (GnomAD)
G=0.000156/1 (1000Genomes)
HGVS:: NC_000003.12:g.154025129A>G, NC_000003.12:g.154025129A>T, NC_000003.11:g.153742918A>G, NC_000003.11:g.153742918A>T, NR_037901.1:n.1870T>C, NR_037901.1:n.1870T>A

Select item 14743998898.

rs1474399889 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:154121101 (GRCh38)
3:153838890 (GRCh37)
Canonical SPDI:: NC_000003.12:154121100:A:G
Gene:: ARHGEF26 (Varview), ARHGEF26-AS1 (Varview)
Functional Consequence:: upstream_transcript_variant,5_prime_UTR_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000003.12:g.154121101A>G, NC_000003.11:g.153838890A>G, NG_030405.1:g.5099A>G, NM_001251962.2:c.-186A>G, NM_001251962.1:c.-186A>G, NT_187533.1:g.164119T>C, XR_001756249.2:n.277T>C, XR_001756249.1:n.228T>C, NR_037901.1:n.110T>C

Select item 14740938009.

rs1474093800 [Homo sapiens]

Variant type:: DELINS
Alleles:: CATTT>- [Show Flanks]
Chromosome:: 3:154024427 (GRCh38)
3:153742216 (GRCh37)
Canonical SPDI:: NC_000003.12:154024424:TTCATTT:TT
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
-=0.00015/21 (GnomAD)
HGVS:: NC_000003.12:g.154024427_154024431del, NC_000003.11:g.153742216_153742220del, NG_010306.1:g.732_736del, NR_037901.1:n.2570_2574del

Select item 147140947410.

rs1471409474 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:154025409 (GRCh38)
3:153743198 (GRCh37)
Canonical SPDI:: NC_000003.12:154025408:A:G
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.154025409A>G, NC_000003.11:g.153743198A>G, NR_037901.1:n.1590T>C

Select item 147104632111.

rs1471046321 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:154024799 (GRCh38)
3:153742588 (GRCh37)
Canonical SPDI:: NC_000003.12:154024798:T:C
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000003.12:g.154024799T>C, NC_000003.11:g.153742588T>C, NR_037901.1:n.2200A>G

Select item 146994917012.

rs1469949170 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:154025272 (GRCh38)
3:153743061 (GRCh37)
Canonical SPDI:: NC_000003.12:154025271:G:T
Gene:: ARHGEF26-AS1 (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=0.000023/6 (TOPMED)
HGVS:: NC_000003.12:g.154025272G>T, NC_000003.11:g.153743061G>T, NR_037901.1:n.1727C>A

Select item 146983757013.

rs1469837570 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:154108754 (GRCh38)
3:153826543 (GRCh37)
Canonical SPDI:: NC_000003.12:154108753:G:A
Gene:: ARHGEF26-AS1 (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=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.154108754G>A, NC_000003.11:g.153826543G>A, NR_037901.1:n.171C>T

Select item 146839148714.

rs1468391487 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTTT>- [Show Flanks]
Chromosome:: 3:154025112 (GRCh38)
3:153742901 (GRCh37)
Canonical SPDI:: NC_000003.12:154025104:TTTCTTTCTTT:TTTCTTT
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTCTTT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000024/2 (GnomAD)
HGVS:: NC_000003.12:g.154025108CTTT[1], NC_000003.11:g.153742897CTTT[1], NR_037901.1:n.1887GAAA[1]

Select item 146718308015.

rs1467183080 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:154024910 (GRCh38)
3:153742699 (GRCh37)
Canonical SPDI:: NC_000003.12:154024909:T:C
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000447/2 (ALFA)
C=0.000035/1 (TOMMO)
C=0.000043/6 (GnomAD)
C=0.000446/2 (Estonian)
C=0.000546/1 (Korea1K)
HGVS:: NC_000003.12:g.154024910T>C, NC_000003.11:g.153742699T>C, NR_037901.1:n.2089A>G

Select item 146671769516.

rs1466717695 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:154024878 (GRCh38)
3:153742667 (GRCh37)
Canonical SPDI:: NC_000003.12:154024877:G:A
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000026/7 (TOPMED)
A=0.000036/5 (GnomAD)
HGVS:: NC_000003.12:g.154024878G>A, NC_000003.11:g.153742667G>A, NR_037901.1:n.2121C>T

Select item 146465140617.

rs1464651406 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:154024554 (GRCh38)
3:153742343 (GRCh37)
Canonical SPDI:: NC_000003.12:154024553:C:T
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.154024554C>T, NC_000003.11:g.153742343C>T, NR_037901.1:n.2445G>A

Select item 146429556818.

rs1464295568 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 3:154025448 (GRCh38)
3:153743237 (GRCh37)
Canonical SPDI:: NC_000003.12:154025447:A:T
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.154025448A>T, NC_000003.11:g.153743237A>T, NR_037901.1:n.1551T>A

Select item 146326006019.

rs1463260060 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:154025146 (GRCh38)
3:153742935 (GRCh37)
Canonical SPDI:: NC_000003.12:154025145:C:T
Gene:: ARHGEF26-AS1 (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_000003.12:g.154025146C>T, NC_000003.11:g.153742935C>T, NR_037901.1:n.1853G>A

Select item 146314414220.

rs1463144142 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 3:154026483 (GRCh38)
3:153744272 (GRCh37)
Canonical SPDI:: NC_000003.12:154026482:TTT:TT
Gene:: ARHGEF26-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
-=0.000015/4 (TOPMED)
HGVS:: NC_000003.12:g.154026485del, NC_000003.11:g.153744274del, NR_037901.1:n.516del

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