SNP Links for Gene (Select 100506725) - SNP

Links from Gene

Items: 1 to 20 of 1113

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Select item 14880767151.

rs1488076715 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:35717373 (GRCh38)
7:35756983 (GRCh37)
Canonical SPDI:: NC_000007.14:35717372:C:T
Gene:: LINC03013 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.35717373C>T, NC_000007.13:g.35756983C>T

Select item 14873539872.

rs1487353987 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:35717290 (GRCh38)
7:35756900 (GRCh37)
Canonical SPDI:: NC_000007.14:35717289:A:C
Gene:: LINC03013 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.35717290A>C, NC_000007.13:g.35756900A>C

Select item 14872129603.

rs1487212960 [Homo sapiens]

Variant type:: DELINS
Alleles:: AATA>- [Show Flanks]
Chromosome:: 7:35717680 (GRCh38)
7:35757290 (GRCh37)
Canonical SPDI:: NC_000007.14:35717678:AAATA:A
Gene:: LINC03013 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.35717680_35717683del, NC_000007.13:g.35757290_35757293del

Select item 14871219764.

rs1487121976 [Homo sapiens]

Variant type:: DEL
Alleles:: TGCA>- [Show Flanks]
Chromosome:: 7:35719755 (GRCh38)
7:35759365 (GRCh37)
Canonical SPDI:: NC_000007.14:35719754:TGCA:
Gene:: LINC03013 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency
MAF:: -=0.0001/14 (GnomAD)
HGVS:: NC_000007.14:g.35719755_35719758del, NC_000007.13:g.35759365_35759368del

Select item 14867678655.

rs1486767865 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:35718526 (GRCh38)
7:35758136 (GRCh37)
Canonical SPDI:: NC_000007.14:35718525:A:G
Gene:: LINC03013 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.35718526A>G, NC_000007.13:g.35758136A>G

Select item 14864670956.

rs1486467095 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>-,CACA [Show Flanks]
Chromosome:: 7:35717875 (GRCh38)
7:35757485 (GRCh37)
Canonical SPDI:: NC_000007.14:35717865:ACACACACACA:ACACACACA,NC_000007.14:35717865:ACACACACACA:ACACACACACACA
Gene:: LINC03013 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: ACACACACACACA=0./0 (ALFA)
AC=0.000043/6 (GnomAD)
HGVS:: NC_000007.14:g.35717867CA[4], NC_000007.14:g.35717867CA[6], NC_000007.13:g.35757477CA[4], NC_000007.13:g.35757477CA[6]

Select item 14856865227.

rs1485686522 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:35717161 (GRCh38)
7:35756771 (GRCh37)
Canonical SPDI:: NC_000007.14:35717160:T:C
Gene:: LINC03013 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.35717161T>C, NC_000007.13:g.35756771T>C

Select item 14856769418.

rs1485676941 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 7:35719308 (GRCh38)
7:35758918 (GRCh37)
Canonical SPDI:: NC_000007.14:35719307:T:
Gene:: LINC03013 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.35719308del, NC_000007.13:g.35758918del, NR_108082.1:n.769del, NR_108083.1:n.671del

Select item 14848487279.

rs1484848727 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:35715200 (GRCh38)
7:35754810 (GRCh37)
Canonical SPDI:: NC_000007.14:35715199:A:G
Gene:: LINC03013 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.35715200A>G, NC_000007.13:g.35754810A>G

Select item 148436197710.

rs1484361977 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:35717559 (GRCh38)
7:35757169 (GRCh37)
Canonical SPDI:: NC_000007.14:35717558:C:T
Gene:: LINC03013 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.35717559C>T, NC_000007.13:g.35757169C>T

Select item 148347569711.

rs1483475697 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:35719077 (GRCh38)
7:35758687 (GRCh37)
Canonical SPDI:: NC_000007.14:35719076:G:A
Gene:: LINC03013 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.35719077G>A, NC_000007.13:g.35758687G>A, NR_108082.1:n.538G>A, NR_108083.1:n.440G>A

Select item 148208740812.

rs1482087408 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:35716517 (GRCh38)
7:35756127 (GRCh37)
Canonical SPDI:: NC_000007.14:35716516:A:G
Gene:: LINC03013 (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_000007.14:g.35716517A>G, NC_000007.13:g.35756127A>G, NR_108082.1:n.81A>G, NR_108083.1:n.81A>G

Select item 148170302013.

rs1481703020 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:35717111 (GRCh38)
7:35756721 (GRCh37)
Canonical SPDI:: NC_000007.14:35717110:A:G
Gene:: LINC03013 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.35717111A>G, NC_000007.13:g.35756721A>G, NR_108082.1:n.513A>G

Select item 148159493914.

rs1481594939 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:35719177 (GRCh38)
7:35758787 (GRCh37)
Canonical SPDI:: NC_000007.14:35719176:A:G
Gene:: LINC03013 (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_000007.14:g.35719177A>G, NC_000007.13:g.35758787A>G, NR_108082.1:n.638A>G, NR_108083.1:n.540A>G

Select item 148151958215.

rs1481519582 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:35718147 (GRCh38)
7:35757757 (GRCh37)
Canonical SPDI:: NC_000007.14:35718146:A:C
Gene:: LINC03013 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.35718147A>C, NC_000007.13:g.35757757A>C

Select item 147924103416.

rs1479241034 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:35718066 (GRCh38)
7:35757676 (GRCh37)
Canonical SPDI:: NC_000007.14:35718065:T:A
Gene:: LINC03013 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000015/2 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000007.14:g.35718066T>A, NC_000007.13:g.35757676T>A

Select item 147851213817.

rs1478512138 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:35715541 (GRCh38)
7:35755151 (GRCh37)
Canonical SPDI:: NC_000007.14:35715540:T:A
Gene:: LINC03013 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.35715541T>A, NC_000007.13:g.35755151T>A

Select item 147845902818.

rs1478459028 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:35716831 (GRCh38)
7:35756441 (GRCh37)
Canonical SPDI:: NC_000007.14:35716830:A:G
Gene:: LINC03013 (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_000007.14:g.35716831A>G, NC_000007.13:g.35756441A>G, NR_108082.1:n.395A>G, NR_108083.1:n.395A>G

Select item 147758742619.

rs1477587426 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>T
Chromosome:: no mapping
Canonical SPDI:

Select item 147660272920.

rs1476602729 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:35719520 (GRCh38)
7:35759130 (GRCh37)
Canonical SPDI:: NC_000007.14:35719519:T:C
Gene:: LINC03013 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.35719520T>C, NC_000007.13:g.35759130T>C, NR_108082.1:n.981T>C, NR_108083.1:n.883T>C

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