SNP Links for Nucleotide (Select 582968252) - SNP

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Select item 14904919971.

rs1490491997 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:46109982 (GRCh38)
22:46505862 (GRCh37)
Canonical SPDI:: NC_000022.11:46109981:G:A
Gene:: MIRLET7BHG (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.46109982G>A, NC_000022.10:g.46505862G>A, NR_027033.2:n.771G>A, NR_027033.1:n.771G>A, XM_047441695.1:c.*5393G>A, XM_047441697.1:c.*5393G>A, XM_047441696.1:c.*5393G>A, XM_047441694.1:c.*5393G>A, NR_110479.1:n.620G>A, NM_207477.1:c.455G>A

Select item 14893172322.

rs1489317232 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:46112710 (GRCh38)
22:46508590 (GRCh37)
Canonical SPDI:: NC_000022.11:46112709:C:T
Gene:: MIRLET7BHG (Varview), MIRLET7A3 (Varview), MIRLET7B (Varview), MIR4763 (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000022.11:g.46112710C>T, NC_000022.10:g.46508590C>T, NR_027033.2:n.3499C>T, NR_027033.1:n.3499C>T, XM_047441695.1:c.*8121C>T, XM_047441697.1:c.*8121C>T, XM_047441696.1:c.*8121C>T, XM_047441694.1:c.*8121C>T, NR_110479.1:n.3348C>T

Select item 14891671993.

rs1489167199 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:46110429 (GRCh38)
22:46506309 (GRCh37)
Canonical SPDI:: NC_000022.11:46110428:A:G
Gene:: MIRLET7BHG (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000022.11:g.46110429A>G, NC_000022.10:g.46506309A>G, NR_027033.2:n.1218A>G, NR_027033.1:n.1218A>G, XM_047441695.1:c.*5840A>G, XM_047441697.1:c.*5840A>G, XM_047441696.1:c.*5840A>G, XM_047441694.1:c.*5840A>G, NR_110479.1:n.1067A>G, NM_207477.1:c.*419A>G

Select item 14887983144.

rs1488798314 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 22:46109760 (GRCh38)
22:46505640 (GRCh37)
Canonical SPDI:: NC_000022.11:46109759:G:A,NC_000022.11:46109759:G:T
Gene:: MIRLET7BHG (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,3_prime_UTR_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_000022.11:g.46109760G>A, NC_000022.11:g.46109760G>T, NC_000022.10:g.46505640G>A, NC_000022.10:g.46505640G>T, NR_027033.2:n.549G>A, NR_027033.2:n.549G>T, NR_027033.1:n.549G>A, NR_027033.1:n.549G>T, XM_047441695.1:c.*5171G>A, XM_047441695.1:c.*5171G>T, XM_047441697.1:c.*5171G>A, XM_047441697.1:c.*5171G>T, XM_047441696.1:c.*5171G>A, XM_047441696.1:c.*5171G>T, XM_047441694.1:c.*5171G>A, XM_047441694.1:c.*5171G>T

Select item 14880061115.

rs1488006111 has merged into rs59737741 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GAGT [Show Flanks]
Chromosome:: 22:46110615 (GRCh38)
22:46506496 (GRCh37)
Canonical SPDI:: NC_000022.11:46110615:T:TGAGT
Gene:: MIRLET7BHG (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by cluster
MAF:: TGAG=0.00303/425 (GnomAD)
TGAG=0.003279/21 (1000Genomes)
HGVS:: NC_000022.11:g.46110616_46110617insGAGT, NC_000022.10:g.46506496_46506497insGAGT, NR_027033.2:n.1405_1406insGAGT, NR_027033.1:n.1405_1406insGAGT, XM_047441695.1:c.*6027_*6028insGAGT, XM_047441697.1:c.*6027_*6028insGAGT, XM_047441696.1:c.*6027_*6028insGAGT, XM_047441694.1:c.*6027_*6028insGAGT, NR_110479.1:n.1254_1255insGAGT, NM_207477.1:c.*606_*607insGAGT

Select item 14869316666.

rs1486931666 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 22:46112590 (GRCh38)
22:46508470 (GRCh37)
Canonical SPDI:: NC_000022.11:46112589:G:A,NC_000022.11:46112589:G:T
Gene:: MIRLET7BHG (Varview), MIRLET7A3 (Varview), MIRLET7B (Varview), MIR4763 (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000022.11:g.46112590G>A, NC_000022.11:g.46112590G>T, NC_000022.10:g.46508470G>A, NC_000022.10:g.46508470G>T, NR_027033.2:n.3379G>A, NR_027033.2:n.3379G>T, NR_027033.1:n.3379G>A, NR_027033.1:n.3379G>T, XM_047441695.1:c.*8001G>A, XM_047441695.1:c.*8001G>T, XM_047441697.1:c.*8001G>A, XM_047441697.1:c.*8001G>T, XM_047441696.1:c.*8001G>A, XM_047441696.1:c.*8001G>T, XM_047441694.1:c.*8001G>A, XM_047441694.1:c.*8001G>T, NR_110479.1:n.3228G>A, NR_110479.1:n.3228G>T

Select item 14847814567.

rs1484781456 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 22:46112055 (GRCh38)
22:46507936 (GRCh37)
Canonical SPDI:: NC_000022.11:46112055::C
Gene:: MIRLET7BHG (Varview), MIRLET7A3 (Varview), MIRLET7B (Varview), MIR4763 (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000061/1 (ALFA)
C=0.000207/29 (GnomAD)
C=0.000223/1 (Estonian)
HGVS:: NC_000022.11:g.46112055_46112056insC, NC_000022.10:g.46507935_46507936insC, NR_027033.2:n.2844_2845insC, NR_027033.1:n.2844_2845insC, XM_047441695.1:c.*7466_*7467insC, XM_047441697.1:c.*7466_*7467insC, XM_047441696.1:c.*7466_*7467insC, XM_047441694.1:c.*7466_*7467insC, NR_110479.1:n.2693_2694insC

Select item 14841326378.

rs1484132637 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 22:46110414 (GRCh38)
22:46506294 (GRCh37)
Canonical SPDI:: NC_000022.11:46110413:C:G
Gene:: MIRLET7BHG (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000224/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000022.11:g.46110414C>G, NC_000022.10:g.46506294C>G, NR_027033.2:n.1203C>G, NR_027033.1:n.1203C>G, XM_047441695.1:c.*5825C>G, XM_047441697.1:c.*5825C>G, XM_047441696.1:c.*5825C>G, XM_047441694.1:c.*5825C>G, NR_110479.1:n.1052C>G, NM_207477.1:c.*404C>G

Select item 14840633129.

rs1484063312 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:46110699 (GRCh38)
22:46506579 (GRCh37)
Canonical SPDI:: NC_000022.11:46110698:C:T
Gene:: MIRLET7BHG (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_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_000022.11:g.46110699C>T, NC_000022.10:g.46506579C>T, NR_027033.2:n.1488C>T, NR_027033.1:n.1488C>T, XM_047441695.1:c.*6110C>T, XM_047441697.1:c.*6110C>T, XM_047441696.1:c.*6110C>T, XM_047441694.1:c.*6110C>T, NR_110479.1:n.1337C>T, NM_207477.1:c.*689C>T

Select item 148392427210.

rs1483924272 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 22:46098545 (GRCh38)
22:46494425 (GRCh37)
Canonical SPDI:: NC_000022.11:46098544:G:C
Gene:: MIRLET7BHG (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.46098545G>C, NC_000022.10:g.46494425G>C, NR_027033.2:n.301G>C, NR_027033.1:n.301G>C, XM_047441695.1:c.-4935G>C, XM_047441697.1:c.-4935G>C, XM_047441696.1:c.-4935G>C, XM_047441694.1:c.-4935G>C, NR_110479.1:n.301G>C, NM_207477.1:c.136G>C

Select item 148333739611.

rs1483337396 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGGGGC>- [Show Flanks]
Chromosome:: 22:46113628 (GRCh38)
22:46509508 (GRCh37)
Canonical SPDI:: NC_000022.11:46113624:GGCAGGGGC:GGC
Gene:: MIRLET7BHG (Varview), MIRLET7B (Varview), MIR4763 (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGC=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000011/3 (TOPMED)
HGVS:: NC_000022.11:g.46113628_46113633del, NC_000022.10:g.46509508_46509513del, NR_027033.2:n.4417_4422del, NR_027033.1:n.4417_4422del, XM_047441695.1:c.*9039_*9044del, XM_047441697.1:c.*9039_*9044del, XM_047441696.1:c.*9039_*9044del, XM_047441694.1:c.*9039_*9044del, NR_110479.1:n.4266_4271del, NR_039920.1:n.63_68del

Select item 148083863212.

rs1480838632 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 22:46111705 (GRCh38)
22:46507585 (GRCh37)
Canonical SPDI:: NC_000022.11:46111704:G:A,NC_000022.11:46111704:G:T
Gene:: MIRLET7BHG (Varview), MIRLET7A3 (Varview), MIRLET7B (Varview), MIR4763 (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000015/2 (GnomAD)
T=0.001092/2 (Korea1K)
HGVS:: NC_000022.11:g.46111705G>A, NC_000022.11:g.46111705G>T, NC_000022.10:g.46507585G>A, NC_000022.10:g.46507585G>T, NR_027033.2:n.2494G>A, NR_027033.2:n.2494G>T, NR_027033.1:n.2494G>A, NR_027033.1:n.2494G>T, XM_047441695.1:c.*7116G>A, XM_047441695.1:c.*7116G>T, XM_047441697.1:c.*7116G>A, XM_047441697.1:c.*7116G>T, XM_047441696.1:c.*7116G>A, XM_047441696.1:c.*7116G>T, XM_047441694.1:c.*7116G>A, XM_047441694.1:c.*7116G>T, NR_110479.1:n.2343G>A, NR_110479.1:n.2343G>T

Select item 148081505013.

rs1480815050 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 22:46112173 (GRCh38)
22:46508053 (GRCh37)
Canonical SPDI:: NC_000022.11:46112172:G:T
Gene:: MIRLET7BHG (Varview), MIRLET7A3 (Varview), MIRLET7B (Varview), MIR4763 (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000035/1 (TOMMO)
T=0.000342/1 (KOREAN)
T=0.000546/1 (Korea1K)
HGVS:: NC_000022.11:g.46112173G>T, NC_000022.10:g.46508053G>T, NR_027033.2:n.2962G>T, NR_027033.1:n.2962G>T, XM_047441695.1:c.*7584G>T, XM_047441697.1:c.*7584G>T, XM_047441696.1:c.*7584G>T, XM_047441694.1:c.*7584G>T, NR_110479.1:n.2811G>T

Select item 148011791614.

rs1480117916 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 22:46113632 (GRCh38)
22:46509512 (GRCh37)
Canonical SPDI:: NC_000022.11:46113631:G:A,NC_000022.11:46113631:G:T
Gene:: MIRLET7BHG (Varview), MIRLET7B (Varview), MIR4763 (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.46113632G>A, NC_000022.11:g.46113632G>T, NC_000022.10:g.46509512G>A, NC_000022.10:g.46509512G>T, NR_027033.2:n.4421G>A, NR_027033.2:n.4421G>T, NR_027033.1:n.4421G>A, NR_027033.1:n.4421G>T, XM_047441695.1:c.*9043G>A, XM_047441695.1:c.*9043G>T, XM_047441697.1:c.*9043G>A, XM_047441697.1:c.*9043G>T, XM_047441696.1:c.*9043G>A, XM_047441696.1:c.*9043G>T, XM_047441694.1:c.*9043G>A, XM_047441694.1:c.*9043G>T, NR_110479.1:n.4270G>A, NR_110479.1:n.4270G>T, NR_039920.1:n.67G>A, NR_039920.1:n.67G>T

Select item 147993960515.

rs1479939605 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:46113578 (GRCh38)
22:46509458 (GRCh37)
Canonical SPDI:: NC_000022.11:46113577:G:A
Gene:: MIRLET7BHG (Varview), MIRLET7B (Varview), MIR4763 (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
HGVS:: NC_000022.11:g.46113578G>A, NC_000022.10:g.46509458G>A, NR_027033.2:n.4367G>A, NR_027033.1:n.4367G>A, XM_047441695.1:c.*8989G>A, XM_047441697.1:c.*8989G>A, XM_047441696.1:c.*8989G>A, XM_047441694.1:c.*8989G>A, NR_110479.1:n.4216G>A, NR_039920.1:n.13G>A

Select item 147873262716.

rs1478732627 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:46111274 (GRCh38)
22:46507154 (GRCh37)
Canonical SPDI:: NC_000022.11:46111273:G:A
Gene:: MIRLET7BHG (Varview), MIRLET7A3 (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000022.11:g.46111274G>A, NC_000022.10:g.46507154G>A, NR_027033.2:n.2063G>A, NR_027033.1:n.2063G>A, XM_047441695.1:c.*6685G>A, XM_047441697.1:c.*6685G>A, XM_047441696.1:c.*6685G>A, XM_047441694.1:c.*6685G>A, NR_110479.1:n.1912G>A, NM_207477.1:c.*1264G>A

Select item 147791458817.

rs1477914588 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 22:46112510 (GRCh38)
22:46508390 (GRCh37)
Canonical SPDI:: NC_000022.11:46112509:G:T
Gene:: MIRLET7BHG (Varview), MIRLET7A3 (Varview), MIRLET7B (Varview), MIR4763 (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000022.11:g.46112510G>T, NC_000022.10:g.46508390G>T, NR_027033.2:n.3299G>T, NR_027033.1:n.3299G>T, XM_047441695.1:c.*7921G>T, XM_047441697.1:c.*7921G>T, XM_047441696.1:c.*7921G>T, XM_047441694.1:c.*7921G>T, NR_110479.1:n.3148G>T

Select item 147726024918.

rs1477260249 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 22:46110111 (GRCh38)
22:46505991 (GRCh37)
Canonical SPDI:: NC_000022.11:46110110:T:C
Gene:: MIRLET7BHG (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_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_000022.11:g.46110111T>C, NC_000022.10:g.46505991T>C, NR_027033.2:n.900T>C, NR_027033.1:n.900T>C, XM_047441695.1:c.*5522T>C, XM_047441697.1:c.*5522T>C, XM_047441696.1:c.*5522T>C, XM_047441694.1:c.*5522T>C, NR_110479.1:n.749T>C, NM_207477.1:c.*101T>C

Select item 147719972919.

rs1477199729 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAG>- [Show Flanks]
Chromosome:: 22:46109273 (GRCh38)
22:46505153 (GRCh37)
Canonical SPDI:: NC_000022.11:46109269:AAGAAG:AAG
Gene:: MIRLET7BHG (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: AAGAAG=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000022.11:g.46109270AAG[1], NC_000022.10:g.46505150AAG[1], NR_027033.2:n.376AAG[1], NR_027033.1:n.376AAG[1], XM_047441695.1:c.*4681AAG[1], XM_047441697.1:c.*4681AAG[1], XM_047441696.1:c.*4681AAG[1], XM_047441694.1:c.*4681AAG[1], NR_110479.1:n.318AAG[1], NM_207477.1:c.153AAG[1]

Select item 147546759020.

rs1475467590 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 22:46112462 (GRCh38)
22:46508342 (GRCh37)
Canonical SPDI:: NC_000022.11:46112461:C:
Gene:: MIRLET7BHG (Varview), MIRLET7A3 (Varview), MIRLET7B (Varview), MIR4763 (Varview), LOC124905135 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000071/1 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.46112462del, NC_000022.10:g.46508342del, NR_027033.2:n.3251del, NR_027033.1:n.3251del, XM_047441695.1:c.*7873del, XM_047441697.1:c.*7873del, XM_047441696.1:c.*7873del, XM_047441694.1:c.*7873del, NR_110479.1:n.3100del

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