SNP Links for Nucleotide (Select 1190747728) - SNP

Links from Nucleotide

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Select item 14915035321.

rs1491503532 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 4:6687610 (GRCh38)
4:6689338 (GRCh37)
Canonical SPDI:: NC_000004.12:6687610:GGGGG:GGGGGG
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GGGGGG=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.6687615dup, NC_000004.11:g.6689342dup, NR_147207.1:n.1658dup

Select item 14912165282.

rs1491216528 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 4:6687810 (GRCh38)
4:6689537 (GRCh37)
Canonical SPDI:: NC_000004.12:6687808:TCT:T
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000004.12:g.6687810_6687811del, NC_000004.11:g.6689537_6689538del, NR_147207.1:n.1459_1460del

Select item 14910283753.

rs1491028375 has merged into rs10658019 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:6687802 (GRCh38)
4:6689529 (GRCh37)
Canonical SPDI:: NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:6687791:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000004.12:g.6687802_6687809del, NC_000004.12:g.6687803_6687809del, NC_000004.12:g.6687804_6687809del, NC_000004.12:g.6687805_6687809del, NC_000004.12:g.6687806_6687809del, NC_000004.12:g.6687807_6687809del, NC_000004.12:g.6687808_6687809del, NC_000004.12:g.6687809del, NC_000004.12:g.6687809dup, NC_000004.12:g.6687808_6687809dup, NC_000004.12:g.6687807_6687809dup, NC_000004.12:g.6687792_6687809T[21]ATTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000004.12:g.6687806_6687809dup, NC_000004.12:g.6687792_6687809T[22]CTTTTTTTTTTTTTTTTTTT[1], NC_000004.12:g.6687805_6687809dup, NC_000004.12:g.6687804_6687809dup, NC_000004.12:g.6687792_6687809T[28]CTTT[2]T[19], NC_000004.12:g.6687797_6687809dup, NC_000004.12:g.6687793_6687809dup, NC_000004.12:g.6687809_6687810insTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.6687809_6687810insTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.6687809_6687810insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.6687809_6687810insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.6687809_6687810insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.6687809_6687810insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.6687809_6687810insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.6689529_6689536del, NC_000004.11:g.6689530_6689536del, NC_000004.11:g.6689531_6689536del, NC_000004.11:g.6689532_6689536del, NC_000004.11:g.6689533_6689536del, NC_000004.11:g.6689534_6689536del, NC_000004.11:g.6689535_6689536del, NC_000004.11:g.6689536del, NC_000004.11:g.6689536dup, NC_000004.11:g.6689535_6689536dup, NC_000004.11:g.6689534_6689536dup, NC_000004.11:g.6689519_6689536T[21]ATTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000004.11:g.6689533_6689536dup, NC_000004.11:g.6689519_6689536T[22]CTTTTTTTTTTTTTTTTTTT[1], NC_000004.11:g.6689532_6689536dup, NC_000004.11:g.6689531_6689536dup, NC_000004.11:g.6689519_6689536T[28]CTTT[2]T[19], NC_000004.11:g.6689524_6689536dup, NC_000004.11:g.6689520_6689536dup, NC_000004.11:g.6689536_6689537insTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.6689536_6689537insTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.6689536_6689537insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.6689536_6689537insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.6689536_6689537insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.6689536_6689537insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.6689536_6689537insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NR_147207.1:n.1470_1477del, NR_147207.1:n.1471_1477del, NR_147207.1:n.1472_1477del, NR_147207.1:n.1473_1477del, NR_147207.1:n.1474_1477del, NR_147207.1:n.1475_1477del, NR_147207.1:n.1476_1477del, NR_147207.1:n.1477del, NR_147207.1:n.1477dup, NR_147207.1:n.1476_1477dup, NR_147207.1:n.1475_1477dup, NR_147207.1:n.1460_1477A[24]TAAAAAAAAAAAAAAAAAAAAA[1], NR_147207.1:n.1474_1477dup, NR_147207.1:n.1460_1477A[19]GAAAAAAAAAAAAAAAAAAAAAA[1], NR_147207.1:n.1473_1477dup, NR_147207.1:n.1472_1477dup, NR_147207.1:n.1460_1477A[22]GAAA[2]A[25], NR_147207.1:n.1465_1477dup, NR_147207.1:n.1461_1477dup, NR_147207.1:n.1477_1478insAAAAAAAAAAAAAAAAAAA, NR_147207.1:n.1477_1478insAAAAAAAAAAAAAAAAAAAAA, NR_147207.1:n.1477_1478insAAAAAAAAAAAAAAAAAAAAAAAA, NR_147207.1:n.1477_1478insAAAAAAAAAAAAAAAAAAAAAAAAA, NR_147207.1:n.1477_1478insAAAAAAAAAAAAAAAAAAAAAAAAAA, NR_147207.1:n.1477_1478insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NR_147207.1:n.1477_1478insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14873492144.

rs1487349214 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:6688300 (GRCh38)
4:6690027 (GRCh37)
Canonical SPDI:: NC_000004.12:6688299:G:C
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000004.12:g.6688300G>C, NC_000004.11:g.6690027G>C, NR_147207.1:n.969C>G

Select item 14850043595.

rs1485004359 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 4:6688066 (GRCh38)
4:6689794 (GRCh37)
Canonical SPDI:: NC_000004.12:6688066:A:AA
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
A=0.000156/1 (1000Genomes)
HGVS:: NC_000004.12:g.6688067dup, NC_000004.11:g.6689794dup, NR_147207.1:n.1202dup

Select item 14844786296.

rs1484478629 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:6688238 (GRCh38)
4:6689965 (GRCh37)
Canonical SPDI:: NC_000004.12:6688237:C:G
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000054/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000223/1 (Estonian)
G=0.000264/37 (GnomAD)
HGVS:: NC_000004.12:g.6688238C>G, NC_000004.11:g.6689965C>G, NR_147207.1:n.1031G>C

Select item 14842100567.

rs1484210056 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:6688696 (GRCh38)
4:6690423 (GRCh37)
Canonical SPDI:: NC_000004.12:6688695:T:C
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.6688696T>C, NC_000004.11:g.6690423T>C, NG_083287.1:g.208T>C, NR_147207.1:n.573A>G

Select item 14827274018.

rs1482727401 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:6688226 (GRCh38)
4:6689953 (GRCh37)
Canonical SPDI:: NC_000004.12:6688225:G:A
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.6688226G>A, NC_000004.11:g.6689953G>A, NR_147207.1:n.1043C>T

Select item 14823816139.

rs1482381613 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:6688607 (GRCh38)
4:6690334 (GRCh37)
Canonical SPDI:: NC_000004.12:6688606:G:A
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000004.12:g.6688607G>A, NC_000004.11:g.6690334G>A, NG_083287.1:g.119G>A, NR_147207.1:n.662C>T

Select item 148227936810.

rs1482279368 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:6689398 (GRCh38)
4:6691125 (GRCh37)
Canonical SPDI:: NC_000004.12:6689397:G:T
Gene:: LINC02481 (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_000004.12:g.6689398G>T, NC_000004.11:g.6691125G>T, NG_083287.1:g.910G>T, NR_147207.1:n.283C>A

Select item 148205213111.

rs1482052131 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 4:6687790 (GRCh38)
4:6689518 (GRCh37)
Canonical SPDI:: NC_000004.12:6687790:G:GG
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
G=0.0007/52 (GnomAD)
HGVS:: NC_000004.12:g.6687791dup, NC_000004.11:g.6689518dup, NR_147207.1:n.1478dup

Select item 148202189612.

rs1482021896 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:6687640 (GRCh38)
4:6689367 (GRCh37)
Canonical SPDI:: NC_000004.12:6687639:G:C
Gene:: LINC02481 (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_000004.12:g.6687640G>C, NC_000004.11:g.6689367G>C, NR_147207.1:n.1629C>G

Select item 148165597813.

rs1481655978 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:6690411 (GRCh38)
4:6692138 (GRCh37)
Canonical SPDI:: NC_000004.12:6690410:A:C
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.6690411A>C, NC_000004.11:g.6692138A>C, NR_147207.1:n.109T>G

Select item 148005889914.

rs1480058899 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:6688464 (GRCh38)
4:6690191 (GRCh37)
Canonical SPDI:: NC_000004.12:6688463:T:C
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.6688464T>C, NC_000004.11:g.6690191T>C, NR_147207.1:n.805A>G

Select item 147938306815.

rs1479383068 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 4:6687795 (GRCh38)
4:6689523 (GRCh37)
Canonical SPDI:: NC_000004.12:6687795::G
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000062/1 (ALFA)
G=0.000023/3 (GnomAD)
HGVS:: NC_000004.12:g.6687795_6687796insG, NC_000004.11:g.6689522_6689523insG, NR_147207.1:n.1473_1474insC

Select item 147848362816.

rs1478483628 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:6687659 (GRCh38)
4:6689386 (GRCh37)
Canonical SPDI:: NC_000004.12:6687658:T:C
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.6687659T>C, NC_000004.11:g.6689386T>C, NR_147207.1:n.1610A>G

Select item 147757718617.

rs1477577186 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 4:6688038 (GRCh38)
4:6689765 (GRCh37)
Canonical SPDI:: NC_000004.12:6688037:CC:C
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000004.12:g.6688039del, NC_000004.11:g.6689766del, NR_147207.1:n.1231del

Select item 147430520218.

rs1474305202 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:6688818 (GRCh38)
4:6690545 (GRCh37)
Canonical SPDI:: NC_000004.12:6688817:T:C
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.6688818T>C, NC_000004.11:g.6690545T>C, NG_083287.1:g.330T>C, NR_147207.1:n.451A>G

Select item 147384650719.

rs1473846507 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:6687921 (GRCh38)
4:6689648 (GRCh37)
Canonical SPDI:: NC_000004.12:6687920:G:C
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.6687921G>C, NC_000004.11:g.6689648G>C, NR_147207.1:n.1348C>G

Select item 147297145220.

rs1472971452 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:6688295 (GRCh38)
4:6690022 (GRCh37)
Canonical SPDI:: NC_000004.12:6688294:C:A,NC_000004.12:6688294:C:T
Gene:: LINC02481 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.6688295C>A, NC_000004.12:g.6688295C>T, NC_000004.11:g.6690022C>A, NC_000004.11:g.6690022C>T, NR_147207.1:n.974G>T, NR_147207.1:n.974G>A

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