SNP Links for Gene (Select 349196) - SNP

Links from Gene

Items: 1 to 20 of 348

<< First< Prev

Page of 18

Next >Last >>

Select item 14901844731.

rs1490184473 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 8:7263491 (GRCh38)
8:7121013 (GRCh37)
Canonical SPDI:: NC_000008.11:7263490:A:C,NC_000008.11:7263490:A:G
Gene:: LINC00965 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00005/1 (GnomAD)
C=0.05727/89 (Korea1K)
C=0.10649/1656 (TOMMO)
C=0.11892/308 (KOREAN)
A=0.26923/7 (SGDP_PRJ)
HGVS:: NC_000008.11:g.7263491A>C, NC_000008.11:g.7263491A>G, NC_000008.10:g.7121013A>C, NC_000008.10:g.7121013A>G, NG_032074.2:g.726A>C, NG_032074.2:g.726A>G, NR_027000.1:n.2T>G, NR_027000.1:n.2T>C

Select item 14873308652.

rs1487330865 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 8:7263755 (GRCh38)
8:7121277 (GRCh37)
Canonical SPDI:: NC_000008.11:7263754:G:C,NC_000008.11:7263754:G:T
Gene:: LINC00965 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000008.11:g.7263755G>C, NC_000008.11:g.7263755G>T, NC_000008.10:g.7121277G>C, NC_000008.10:g.7121277G>T, NG_032074.2:g.990G>C, NG_032074.2:g.990G>T

Select item 14864481643.

rs1486448164 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:7262175 (GRCh38)
8:7119697 (GRCh37)
Canonical SPDI:: NC_000008.11:7262174:T:C
Gene:: LINC00965 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000008.11:g.7262175T>C, NC_000008.10:g.7119697T>C, NR_027000.1:n.1318A>G

Select item 14847741404.

rs1484774140 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:7262458 (GRCh38)
8:7119980 (GRCh37)
Canonical SPDI:: NC_000008.11:7262457:G:C
Gene:: LINC00965 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000008.11:g.7262458G>C, NC_000008.10:g.7119980G>C, NR_027000.1:n.1035C>G

Select item 14838601445.

rs1483860144 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 8:7263568 (GRCh38)
8:7121090 (GRCh37)
Canonical SPDI:: NC_000008.11:7263567:G:A,NC_000008.11:7263567:G:C,NC_000008.11:7263567:G:T
Gene:: LINC00965 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000008.11:g.7263568G>A, NC_000008.11:g.7263568G>C, NC_000008.11:g.7263568G>T, NC_000008.10:g.7121090G>A, NC_000008.10:g.7121090G>C, NC_000008.10:g.7121090G>T, NG_032074.2:g.803G>A, NG_032074.2:g.803G>C, NG_032074.2:g.803G>T

Select item 14834764276.

rs1483476427 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:7263477 (GRCh38)
8:7120999 (GRCh37)
Canonical SPDI:: NC_000008.11:7263476:A:G
Gene:: LINC00965 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.00008/1 (ALFA)
G=0.00031/6 (GnomAD)
G=0.00241/6 (KOREAN)
A=0.25/1 (SGDP_PRJ)
HGVS:: NC_000008.11:g.7263477A>G, NC_000008.10:g.7120999A>G, NG_032074.2:g.712A>G, NR_027000.1:n.16T>C

Select item 14834112647.

rs1483411264 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 8:7263756 (GRCh38)
8:7121278 (GRCh37)
Canonical SPDI:: NC_000008.11:7263755:G:A,NC_000008.11:7263755:G:T
Gene:: LINC00965 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.00682/95 (TOMMO)
A=0.02491/40 (Korea1K)
A=0.10517/285 (KOREAN)
G=0.46154/24 (SGDP_PRJ)
HGVS:: NC_000008.11:g.7263756G>A, NC_000008.11:g.7263756G>T, NC_000008.10:g.7121278G>A, NC_000008.10:g.7121278G>T, NG_032074.2:g.991G>A, NG_032074.2:g.991G>T

Select item 14816540708.

rs1481654070 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:7262927 (GRCh38)
8:7120449 (GRCh37)
Canonical SPDI:: NC_000008.11:7262926:G:A
Gene:: LINC00965 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000008.11:g.7262927G>A, NC_000008.10:g.7120449G>A, NG_032074.2:g.162G>A, NR_027000.1:n.566C>T

Select item 14809451319.

rs1480945131 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 8:7263660 (GRCh38)
8:7121182 (GRCh37)
Canonical SPDI:: NC_000008.11:7263659:C:A,NC_000008.11:7263659:C:G
Gene:: LINC00965 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
A=0.00007/1 (GnomAD)
HGVS:: NC_000008.11:g.7263660C>A, NC_000008.11:g.7263660C>G, NC_000008.10:g.7121182C>A, NC_000008.10:g.7121182C>G, NG_032074.2:g.895C>A, NG_032074.2:g.895C>G

Select item 148008030310.

rs1480080303 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 8:7263851 (GRCh38)
8:7121373 (GRCh37)
Canonical SPDI:: NC_000008.11:7263850:C:G,NC_000008.11:7263850:C:T
Gene:: LINC00965 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.00093/10 (TOMMO)
HGVS:: NC_000008.11:g.7263851C>G, NC_000008.11:g.7263851C>T, NC_000008.10:g.7121373C>G, NC_000008.10:g.7121373C>T, NG_032074.2:g.1086C>G, NG_032074.2:g.1086C>T

Select item 148003401411.

rs1480034014 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:7263389 (GRCh38)
8:7120911 (GRCh37)
Canonical SPDI:: NC_000008.11:7263388:A:G
Gene:: LINC00965 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.04864/577 (ALFA)
G=0.00533/5 (Korea1K)
G=0.00616/26 (GnomAD)
G=0.03297/403 (TOMMO)
G=0.04577/91 (KOREAN)
HGVS:: NC_000008.11:g.7263389A>G, NC_000008.10:g.7120911A>G, NG_032074.2:g.624A>G, NR_027000.1:n.104T>C

Select item 147862474212.

rs1478624742 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:7263820 (GRCh38)
8:7121342 (GRCh37)
Canonical SPDI:: NC_000008.11:7263819:G:A
Gene:: LINC00965 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000008.11:g.7263820G>A, NC_000008.10:g.7121342G>A, NG_032074.2:g.1055G>A

Select item 147763180313.

rs1477631803 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>-,GG [Show Flanks]
Chromosome:: 8:7263572 (GRCh38)
8:7121094 (GRCh37)
Canonical SPDI:: NC_000008.11:7263571:GGGGG:GGGG,NC_000008.11:7263571:GGGGG:GGGGGG
Gene:: LINC00965 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGG=0.00008/1 (ALFA)
-=0.00008/2 (TOMMO)
HGVS:: NC_000008.11:g.7263576del, NC_000008.11:g.7263576dup, NC_000008.10:g.7121098del, NC_000008.10:g.7121098dup, NG_032074.2:g.811del, NG_032074.2:g.811dup

Select item 147594595514.

rs1475945955 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 8:7263556 (GRCh38)
8:7121078 (GRCh37)
Canonical SPDI:: NC_000008.11:7263555:T:C,NC_000008.11:7263555:T:G
Gene:: LINC00965 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0./0 (SGDP_PRJ)
G=0.0018/3 (Korea1K)
G=0.00548/84 (TOMMO)
G=0.02381/64 (KOREAN)
HGVS:: NC_000008.11:g.7263556T>C, NC_000008.11:g.7263556T>G, NC_000008.10:g.7121078T>C, NC_000008.10:g.7121078T>G, NG_032074.2:g.791T>C, NG_032074.2:g.791T>G

Select item 147412496915.

rs1474124969 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 8:7263501 (GRCh38)
8:7121023 (GRCh37)
Canonical SPDI:: NC_000008.11:7263500:T:A,NC_000008.11:7263500:T:C
Gene:: LINC00965 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.00003/1 (GnomAD)
HGVS:: NC_000008.11:g.7263501T>A, NC_000008.11:g.7263501T>C, NC_000008.10:g.7121023T>A, NC_000008.10:g.7121023T>C, NG_032074.2:g.736T>A, NG_032074.2:g.736T>C

Select item 147387109416.

rs1473871094 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 8:7262885 (GRCh38)
8:7120407 (GRCh37)
Canonical SPDI:: NC_000008.11:7262884:G:A,NC_000008.11:7262884:G:T
Gene:: LINC00965 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0./0 (SGDP_PRJ)
T=0.00049/4 (TOMMO)
HGVS:: NC_000008.11:g.7262885G>A, NC_000008.11:g.7262885G>T, NC_000008.10:g.7120407G>A, NC_000008.10:g.7120407G>T, NG_032074.2:g.120G>A, NG_032074.2:g.120G>T, NR_027000.1:n.608C>T, NR_027000.1:n.608C>A

Select item 147382517617.

rs1473825176 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 8:7263788 (GRCh38)
8:7121310 (GRCh37)
Canonical SPDI:: NC_000008.11:7263787:GGGGGG:GGGGG
Gene:: LINC00965 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: GGGGG=0./0 (ALFA)
-=0.00005/1 (GnomAD)
HGVS:: NC_000008.11:g.7263793del, NC_000008.10:g.7121315del, NG_032074.2:g.1028del

Select item 147288598218.

rs1472885982 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 8:7263885 (GRCh38)
8:7121407 (GRCh37)
Canonical SPDI:: NC_000008.11:7263884:G:A,NC_000008.11:7263884:G:C
Gene:: LINC00965 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000008.11:g.7263885G>A, NC_000008.11:g.7263885G>C, NC_000008.10:g.7121407G>A, NC_000008.10:g.7121407G>C, NG_032074.2:g.1120G>A, NG_032074.2:g.1120G>C

Select item 147277749319.

rs1472777493 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:7263370 (GRCh38)
8:7120892 (GRCh37)
Canonical SPDI:: NC_000008.11:7263369:A:G
Gene:: LINC00965 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.0011/13 (ALFA)
A=0./0 (SGDP_PRJ)
G=0.00268/29 (TOMMO)
G=0.00581/5 (Korea1K)
G=0.00787/14 (KOREAN)
HGVS:: NC_000008.11:g.7263370A>G, NC_000008.10:g.7120892A>G, NG_032074.2:g.605A>G, NR_027000.1:n.123T>C

Select item 147222752720.

rs1472227527 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:7263453 (GRCh38)
8:7120975 (GRCh37)
Canonical SPDI:: NC_000008.11:7263452:G:C
Gene:: LINC00965 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.00084/10 (ALFA)
HGVS:: NC_000008.11:g.7263453G>C, NC_000008.10:g.7120975G>C, NG_032074.2:g.688G>C, NR_027000.1:n.40C>G

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 348

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity