SNP Links for Nucleotide (Select 594191230) - SNP

Links from Nucleotide

Items: 1 to 20 of 600

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Select item 14908325461.

rs1490832546 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:76657636 (GRCh38)
16:76691533 (GRCh37)
Canonical SPDI:: NC_000016.10:76657635:G:T
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.76657636G>T, NC_000016.9:g.76691533G>T, NR_110934.1:n.1356G>T

Select item 14873809652.

rs1487380965 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:76657527 (GRCh38)
16:76691424 (GRCh37)
Canonical SPDI:: NC_000016.10:76657526:A:G
Gene:: LINC02125 (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_000016.10:g.76657527A>G, NC_000016.9:g.76691424A>G, NR_110934.1:n.1247A>G

Select item 14873632093.

rs1487363209 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:76658096 (GRCh38)
16:76691993 (GRCh37)
Canonical SPDI:: NC_000016.10:76658095:A:G
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000016.10:g.76658096A>G, NC_000016.9:g.76691993A>G, NR_110934.1:n.1816A>G

Select item 14827464604.

rs1482746460 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:76657723 (GRCh38)
16:76691620 (GRCh37)
Canonical SPDI:: NC_000016.10:76657722:T:C
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.76657723T>C, NC_000016.9:g.76691620T>C, NR_110934.1:n.1443T>C

Select item 14820804065.

rs1482080406 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:76635043 (GRCh38)
16:76668940 (GRCh37)
Canonical SPDI:: NC_000016.10:76635042:T:C
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.76635043T>C, NC_000016.9:g.76668940T>C, NR_110934.1:n.46T>C

Select item 14807238376.

rs1480723837 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 16:76658448 (GRCh38)
16:76692345 (GRCh37)
Canonical SPDI:: NC_000016.10:76658447:A:G,NC_000016.10:76658447:A:T
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000016.10:g.76658448A>G, NC_000016.10:g.76658448A>T, NC_000016.9:g.76692345A>G, NC_000016.9:g.76692345A>T, NR_110934.1:n.2168A>G, NR_110934.1:n.2168A>T

Select item 14806252107.

rs1480625210 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 16:76657713 (GRCh38)
16:76691610 (GRCh37)
Canonical SPDI:: NC_000016.10:76657712:A:C
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000016.10:g.76657713A>C, NC_000016.9:g.76691610A>C, NR_110934.1:n.1433A>C

Select item 14801835728.

rs1480183572 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:76658230 (GRCh38)
16:76692127 (GRCh37)
Canonical SPDI:: NC_000016.10:76658229:A:G
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.76658230A>G, NC_000016.9:g.76692127A>G, NR_110934.1:n.1950A>G

Select item 14771449929.

rs1477144992 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:76656721 (GRCh38)
16:76690618 (GRCh37)
Canonical SPDI:: NC_000016.10:76656720:T:C
Gene:: LINC02125 (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_000016.10:g.76656721T>C, NC_000016.9:g.76690618T>C, NR_110934.1:n.441T>C

Select item 147567733410.

rs1475677334 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:76657807 (GRCh38)
16:76691704 (GRCh37)
Canonical SPDI:: NC_000016.10:76657806:A:G
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.76657807A>G, NC_000016.9:g.76691704A>G, NR_110934.1:n.1527A>G

Select item 147241825711.

rs1472418257 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:76635500 (GRCh38)
16:76669397 (GRCh37)
Canonical SPDI:: NC_000016.10:76635499:A:G
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000031/4 (GnomAD_exomes)
HGVS:: NC_000016.10:g.76635500A>G, NC_000016.9:g.76669397A>G, NR_110934.1:n.156A>G

Select item 147107849312.

rs1471078493 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:76657532 (GRCh38)
16:76691429 (GRCh37)
Canonical SPDI:: NC_000016.10:76657531:G:A
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000132/2 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000446/2 (Estonian)
HGVS:: NC_000016.10:g.76657532G>A, NC_000016.9:g.76691429G>A, NR_110934.1:n.1252G>A

Select item 147083458313.

rs1470834583 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:76657800 (GRCh38)
16:76691697 (GRCh37)
Canonical SPDI:: NC_000016.10:76657799:A:G
Gene:: LINC02125 (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=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.76657800A>G, NC_000016.9:g.76691697A>G, NR_110934.1:n.1520A>G

Select item 147045403614.

rs1470454036 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 16:76635522 (GRCh38)
16:76669419 (GRCh37)
Canonical SPDI:: NC_000016.10:76635521:C:G
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.76635522C>G, NC_000016.9:g.76669419C>G, NR_110934.1:n.178C>G

Select item 147021216615.

rs1470212166 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:76657556 (GRCh38)
16:76691453 (GRCh37)
Canonical SPDI:: NC_000016.10:76657555:A:G
Gene:: LINC02125 (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_000016.10:g.76657556A>G, NC_000016.9:g.76691453A>G, NR_110934.1:n.1276A>G

Select item 146961442816.

rs1469614428 has merged into rs1028974472 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>-,CC [Show Flanks]
Chromosome:: 16:76658146 (GRCh38)
16:76692043 (GRCh37)
Canonical SPDI:: NC_000016.10:76658145:CCCCCC:CCCCC,NC_000016.10:76658145:CCCCCC:CCCCCCC
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCCCCCC=0./0 (ALFA)
HGVS:: NC_000016.10:g.76658151del, NC_000016.10:g.76658151dup, NC_000016.9:g.76692048del, NC_000016.9:g.76692048dup, NR_110934.1:n.1871del, NR_110934.1:n.1871dup

Select item 146811353017.

rs1468113530 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 16:76635073 (GRCh38)
16:76668970 (GRCh37)
Canonical SPDI:: NC_000016.10:76635072:G:A,NC_000016.10:76635072:G:C
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00021/4 (TOMMO)
HGVS:: NC_000016.10:g.76635073G>A, NC_000016.10:g.76635073G>C, NC_000016.9:g.76668970G>A, NC_000016.9:g.76668970G>C, NR_110934.1:n.76G>A, NR_110934.1:n.76G>C

Select item 146772862318.

rs1467728623 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:76656918 (GRCh38)
16:76690815 (GRCh37)
Canonical SPDI:: NC_000016.10:76656917:C:A
Gene:: LINC02125 (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=0.000038/10 (TOPMED)
HGVS:: NC_000016.10:g.76656918C>A, NC_000016.9:g.76690815C>A, NR_110934.1:n.638C>A

Select item 146593331619.

rs1465933316 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 16:76658346 (GRCh38)
16:76692243 (GRCh37)
Canonical SPDI:: NC_000016.10:76658345:T:G
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.03001/356 (ALFA)
G=0.04178/122 (KOREAN)
HGVS:: NC_000016.10:g.76658346T>G, NC_000016.9:g.76692243T>G, NR_110934.1:n.2066T>G

Select item 146470216420.

rs1464702164 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:76657690 (GRCh38)
16:76691587 (GRCh37)
Canonical SPDI:: NC_000016.10:76657689:G:A
Gene:: LINC02125 (Varview)
Functional Consequence:: non_coding_transcript_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_000016.10:g.76657690G>A, NC_000016.9:g.76691587G>A, NR_110934.1:n.1410G>A

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