SNP Links for Nucleotide (Select 563407175) - SNP

Links from Nucleotide

Items: 1 to 20 of 449

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Select item 14908903831.

rs1490890383 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 5:44413145 (GRCh38)
5:44413247 (GRCh37)
Canonical SPDI:: NC_000005.10:44413144:C:A
Gene:: FGF10-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_000005.10:g.44413145C>A, NC_000005.9:g.44413247C>A, NR_108034.1:n.1050C>A

Select item 14887465352.

rs1488746535 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:44413264 (GRCh38)
5:44413366 (GRCh37)
Canonical SPDI:: NC_000005.10:44413263:C:T
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000005.10:g.44413264C>T, NC_000005.9:g.44413366C>T, NR_108034.1:n.1169C>T

Select item 14887068413.

rs1488706841 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 5:44413554 (GRCh38)
5:44413656 (GRCh37)
Canonical SPDI:: NC_000005.10:44413553:G:C
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.44413554G>C, NC_000005.9:g.44413656G>C, NR_108034.1:n.1459G>C

Select item 14816161094.

rs1481616109 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 5:44413242 (GRCh38)
5:44413344 (GRCh37)
Canonical SPDI:: NC_000005.10:44413241:A:T
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000684/2 (KOREAN)
A=0.5/1 (SGDP_PRJ)
HGVS:: NC_000005.10:g.44413242A>T, NC_000005.9:g.44413344A>T, NR_108034.1:n.1147A>T

Select item 14782465795.

rs1478246579 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:44413322 (GRCh38)
5:44413424 (GRCh37)
Canonical SPDI:: NC_000005.10:44413321:G:A
Gene:: FGF10-AS1 (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=0.000014/2 (GnomAD)
A=0.000156/1 (1000Genomes)
A=0.000684/2 (KOREAN)
HGVS:: NC_000005.10:g.44413322G>A, NC_000005.9:g.44413424G>A, NR_108034.1:n.1227G>A

Select item 14746135846.

rs1474613584 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:44395326 (GRCh38)
5:44395428 (GRCh37)
Canonical SPDI:: NC_000005.10:44395325:C:T
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.44395326C>T, NC_000005.9:g.44395428C>T, NR_108034.1:n.272C>T

Select item 14741943587.

rs1474194358 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:44412887 (GRCh38)
5:44412989 (GRCh37)
Canonical SPDI:: NC_000005.10:44412886:G:A
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000005.10:g.44412887G>A, NC_000005.9:g.44412989G>A, NR_108034.1:n.792G>A

Select item 14735791418.

rs1473579141 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:44412973 (GRCh38)
5:44413075 (GRCh37)
Canonical SPDI:: NC_000005.10:44412972:T:C
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.44412973T>C, NC_000005.9:g.44413075T>C, NR_108034.1:n.878T>C

Select item 14690833089.

rs1469083308 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 5:44413802 (GRCh38)
5:44413904 (GRCh37)
Canonical SPDI:: NC_000005.10:44413796:TCTCTCT:TCTCT
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TCTCT=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000005.10:g.44413798CT[2], NC_000005.9:g.44413900CT[2], NR_108034.1:n.1703CT[2]

Select item 146666678610.

rs1466666786 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:44412414 (GRCh38)
5:44412516 (GRCh37)
Canonical SPDI:: NC_000005.10:44412413:T:C
Gene:: FGF10-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_000005.10:g.44412414T>C, NC_000005.9:g.44412516T>C, NR_108034.1:n.319T>C

Select item 146516893911.

rs1465168939 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:44413340 (GRCh38)
5:44413442 (GRCh37)
Canonical SPDI:: NC_000005.10:44413339:A:G
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.44413340A>G, NC_000005.9:g.44413442A>G, NR_108034.1:n.1245A>G

Select item 146351575312.

rs1463515753 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 5:44413189 (GRCh38)
5:44413291 (GRCh37)
Canonical SPDI:: NC_000005.10:44413188:G:A,NC_000005.10:44413188:G:C
Gene:: FGF10-AS1 (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)
C=0.000177/3 (TOMMO)
HGVS:: NC_000005.10:g.44413189G>A, NC_000005.10:g.44413189G>C, NC_000005.9:g.44413291G>A, NC_000005.9:g.44413291G>C, NR_108034.1:n.1094G>A, NR_108034.1:n.1094G>C

Select item 146279232913.

rs1462792329 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:44413443 (GRCh38)
5:44413545 (GRCh37)
Canonical SPDI:: NC_000005.10:44413442:A:G
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.44413443A>G, NC_000005.9:g.44413545A>G, NR_108034.1:n.1348A>G

Select item 146176766614.

rs1461767666 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 5:44412503 (GRCh38)
5:44412605 (GRCh37)
Canonical SPDI:: NC_000005.10:44412502:A:C
Gene:: FGF10-AS1 (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_000005.10:g.44412503A>C, NC_000005.9:g.44412605A>C, NR_108034.1:n.408A>C

Select item 146123275015.

rs1461232750 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:44412988 (GRCh38)
5:44413090 (GRCh37)
Canonical SPDI:: NC_000005.10:44412987:C:T
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
HGVS:: NC_000005.10:g.44412988C>T, NC_000005.9:g.44413090C>T, NR_108034.1:n.893C>T

Select item 145989526116.

rs1459895261 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 5:44413471 (GRCh38)
5:44413573 (GRCh37)
Canonical SPDI:: NC_000005.10:44413470:T:G
Gene:: FGF10-AS1 (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_000005.10:g.44413471T>G, NC_000005.9:g.44413573T>G, NR_108034.1:n.1376T>G

Select item 145976888217.

rs1459768882 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:44413304 (GRCh38)
5:44413406 (GRCh37)
Canonical SPDI:: NC_000005.10:44413303:G:A
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.00018/3 (ALFA)
HGVS:: NC_000005.10:g.44413304G>A, NC_000005.9:g.44413406G>A, NR_108034.1:n.1209G>A

Select item 145431830018.

rs1454318300 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:44388797 (GRCh38)
5:44388899 (GRCh37)
Canonical SPDI:: NC_000005.10:44388796:T:C
Gene:: FGF10 (Varview), FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000005.10:g.44388797T>C, NC_000005.9:g.44388899T>C, NG_011446.1:g.4886A>G, XM_005248264.5:c.-115A>G, XM_005248264.4:c.-115A>G, XM_005248264.3:c.-115A>G, XM_005248264.2:c.-115A>G, XM_005248264.1:c.-115A>G, NM_004465.2:c.-115A>G, NR_108034.1:n.66T>C

Select item 145323129119.

rs1453231291 [Homo sapiens]

Variant type:: DELINS
Alleles:: TCT>- [Show Flanks]
Chromosome:: 5:44413797 (GRCh38)
5:44413899 (GRCh37)
Canonical SPDI:: NC_000005.10:44413793:TCTTCT:TCT
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTTCT=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000015/4 (TOPMED)
HGVS:: NC_000005.10:g.44413794TCT[1], NC_000005.9:g.44413896TCT[1], NR_108034.1:n.1699TCT[1]

Select item 145081165420.

rs1450811654 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:44413438 (GRCh38)
5:44413540 (GRCh37)
Canonical SPDI:: NC_000005.10:44413437:G:A
Gene:: FGF10-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000045/12 (TOPMED)
A=0.001486/25 (TOMMO)
A=0.004791/14 (KOREAN)
HGVS:: NC_000005.10:g.44413438G>A, NC_000005.9:g.44413540G>A, NR_108034.1:n.1343G>A

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