SNP Links for Nucleotide (Select 587651966) - SNP

Links from Nucleotide

Items: 1 to 20 of 387

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Select item 14900647491.

rs1490064749 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 19:23057037 (GRCh38)
19:23239839 (GRCh37)
Canonical SPDI:: NC_000019.10:23057036:G:
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.23057037del, NC_000019.9:g.23239839del, NR_110745.1:n.889del

Select item 14890473442.

rs1489047344 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 19:23058471 (GRCh38)
19:23241273 (GRCh37)
Canonical SPDI:: NC_000019.10:23058470:A:G,NC_000019.10:23058470:A:T
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000142/2 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000015/4 (TOPMED)
T=0.000156/1 (1000Genomes)
HGVS:: NC_000019.10:g.23058471A>G, NC_000019.10:g.23058471A>T, NC_000019.9:g.23241273A>G, NC_000019.9:g.23241273A>T, NR_110745.1:n.699T>C, NR_110745.1:n.699T>A

Select item 14866680853.

rs1486668085 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:23057127 (GRCh38)
19:23239929 (GRCh37)
Canonical SPDI:: NC_000019.10:23057126:G:A
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000066/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000223/1 (Estonian)
HGVS:: NC_000019.10:g.23057127G>A, NC_000019.9:g.23239929G>A, NR_110745.1:n.799C>T

Select item 14839870084.

rs1483987008 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 19:23055028 (GRCh38)
19:23237830 (GRCh37)
Canonical SPDI:: NC_000019.10:23055027:G:
Gene:: LINC01858 (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_000019.10:g.23055028del, NC_000019.9:g.23237830del, NR_110745.1:n.1633del

Select item 14834316085.

rs1483431608 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:23060881 (GRCh38)
19:23243683 (GRCh37)
Canonical SPDI:: NC_000019.10:23060880:G:T
Gene:: LINC01858 (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=0.000015/4 (TOPMED)
HGVS:: NC_000019.10:g.23060881G>T, NC_000019.9:g.23243683G>T, NR_110745.1:n.211C>A

Select item 14831942636.

rs1483194263 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:23054944 (GRCh38)
19:23237746 (GRCh37)
Canonical SPDI:: NC_000019.10:23054943:T:C
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.23054944T>C, NC_000019.9:g.23237746T>C, NR_110745.1:n.1717A>G

Select item 14823822037.

rs1482382203 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:23060695 (GRCh38)
19:23243497 (GRCh37)
Canonical SPDI:: NC_000019.10:23060694:T:G
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000026/7 (TOPMED)
G=0.000043/6 (GnomAD)
HGVS:: NC_000019.10:g.23060695T>G, NC_000019.9:g.23243497T>G, NR_110745.1:n.397A>C

Select item 14806671198.

rs1480667119 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:23057177 (GRCh38)
19:23239979 (GRCh37)
Canonical SPDI:: NC_000019.10:23057176:T:G
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.23057177T>G, NC_000019.9:g.23239979T>G, NR_110745.1:n.749A>C

Select item 14799182469.

rs1479918246 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:23057124 (GRCh38)
19:23239926 (GRCh37)
Canonical SPDI:: NC_000019.10:23057123:T:C
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000248/4 (TOMMO)
C=0.000546/1 (Korea1K)
HGVS:: NC_000019.10:g.23057124T>C, NC_000019.9:g.23239926T>C, NR_110745.1:n.802A>G

Select item 147638284310.

rs1476382843 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 19:23060758 (GRCh38)
19:23243560 (GRCh37)
Canonical SPDI:: NC_000019.10:23060757:G:A,NC_000019.10:23060757:G:C
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.23060758G>A, NC_000019.10:g.23060758G>C, NC_000019.9:g.23243560G>A, NC_000019.9:g.23243560G>C, NR_110745.1:n.334C>T, NR_110745.1:n.334C>G

Select item 147623463211.

rs1476234632 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:23061186 (GRCh38)
19:23243988 (GRCh37)
Canonical SPDI:: NC_000019.10:23061185:C:G
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000019.10:g.23061186C>G, NC_000019.9:g.23243988C>G, NR_110745.1:n.80G>C

Select item 147571012012.

rs1475710120 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:23055054 (GRCh38)
19:23237856 (GRCh37)
Canonical SPDI:: NC_000019.10:23055053:T:C
Gene:: LINC01858 (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=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.23055054T>C, NC_000019.9:g.23237856T>C, NR_110745.1:n.1607A>G

Select item 147457006513.

rs1474570065 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:23055294 (GRCh38)
19:23238096 (GRCh37)
Canonical SPDI:: NC_000019.10:23055293:T:C
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.23055294T>C, NC_000019.9:g.23238096T>C, NR_110745.1:n.1367A>G

Select item 146880875414.

rs1468808754 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:23055620 (GRCh38)
19:23238422 (GRCh37)
Canonical SPDI:: NC_000019.10:23055619:A:G
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.23055620A>G, NC_000019.9:g.23238422A>G, NR_110745.1:n.1192T>C

Select item 146817930315.

rs1468179303 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:23060788 (GRCh38)
19:23243590 (GRCh37)
Canonical SPDI:: NC_000019.10:23060787:C:T
Gene:: LINC01858 (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=0.000212/4 (TOMMO)
HGVS:: NC_000019.10:g.23060788C>T, NC_000019.9:g.23243590C>T, NR_110745.1:n.304G>A

Select item 146422434516.

rs1464224345 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:23060804 (GRCh38)
19:23243606 (GRCh37)
Canonical SPDI:: NC_000019.10:23060803:C:A
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000019.10:g.23060804C>A, NC_000019.9:g.23243606C>A, NR_110745.1:n.288G>T

Select item 145869687717.

rs1458696877 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:23055164 (GRCh38)
19:23237966 (GRCh37)
Canonical SPDI:: NC_000019.10:23055163:G:C
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000023/6 (TOPMED)
HGVS:: NC_000019.10:g.23055164G>C, NC_000019.9:g.23237966G>C, NR_110745.1:n.1497C>G

Select item 145709922418.

rs1457099224 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:23055060 (GRCh38)
19:23237862 (GRCh37)
Canonical SPDI:: NC_000019.10:23055059:G:T
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.23055060G>T, NC_000019.9:g.23237862G>T, NR_110745.1:n.1601C>A

Select item 145671610219.

rs1456716102 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 19:23058549 (GRCh38)
19:23241351 (GRCh37)
Canonical SPDI:: NC_000019.10:23058548:C:G,NC_000019.10:23058548:C:T
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.23058549C>G, NC_000019.10:g.23058549C>T, NC_000019.9:g.23241351C>G, NC_000019.9:g.23241351C>T, NR_110745.1:n.621G>C, NR_110745.1:n.621G>A

Select item 145649780620.

rs1456497806 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:23056356 (GRCh38)
19:23239158 (GRCh37)
Canonical SPDI:: NC_000019.10:23056355:A:G
Gene:: LINC01858 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000021/3 (GnomAD)
HGVS:: NC_000019.10:g.23056356A>G, NC_000019.9:g.23239158A>G, NR_110745.1:n.968T>C

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