SNP Links for Gene (Select 83593) - SNP

Links from Gene

Items: 1 to 20 of 1000

<< First< Prev

Page of 50

Next >Last >>

Select item 14915583041.

rs1491558304 has merged into rs1413530490 [Homo sapiens]

Variant type:: DELINS
Alleles:: AATATAT>-,AATATATAATATAT [Show Flanks]
Chromosome:: 1:206523452 (GRCh38)
1:206696785 (GRCh37)
Canonical SPDI:: NC_000001.11:206523438:ATATATAATATATAATATAT:ATATATAATATAT,NC_000001.11:206523438:ATATATAATATATAATATAT:ATATATAATATATAATATATAATATAT
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATAATATATAATATATAATATAT=0./0 (ALFA)
ATATATA=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.206523445AATATAT[1], NC_000001.11:g.206523445AATATAT[3], NW_003871057.1:g.514299AATATAT[1], NW_003871057.1:g.514299AATATAT[3], NG_029062.2:g.20900AATATAT[1], NG_029062.2:g.20900AATATAT[3], NC_000001.10:g.206696778AATATAT[1], NC_000001.10:g.206696778AATATAT[3]

Select item 14914799832.

rs1491479983 has merged into rs368124193 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACACACACACACAC>-,AC,ACAC,ACACAC,ACACACAC,ACACACACAC,ACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACAC [Show Flanks]
Chromosome:: 1:206508342 (GRCh38)
1:206681675 (GRCh37)
Canonical SPDI:: NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:206508322:CACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACACAC
Gene:: RASSF5 (Varview), LOC124904493 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACACACACACAC=0./0 (ALFA)
HGVS:: NC_000001.11:g.206508324AC[9], NC_000001.11:g.206508324AC[10], NC_000001.11:g.206508324AC[11], NC_000001.11:g.206508324AC[12], NC_000001.11:g.206508324AC[13], NC_000001.11:g.206508324AC[14], NC_000001.11:g.206508324AC[15], NC_000001.11:g.206508324AC[17], NC_000001.11:g.206508324AC[18], NC_000001.11:g.206508324AC[19], NC_000001.11:g.206508324AC[20], NC_000001.11:g.206508324AC[21], NC_000001.11:g.206508324AC[22], NC_000001.11:g.206508324AC[23], NC_000001.11:g.206508324AC[24], NC_000001.11:g.206508324AC[25], NC_000001.11:g.206508324AC[26], NW_003871057.1:g.499178AC[9], NW_003871057.1:g.499178AC[10], NW_003871057.1:g.499178AC[11], NW_003871057.1:g.499178AC[12], NW_003871057.1:g.499178AC[13], NW_003871057.1:g.499178AC[14], NW_003871057.1:g.499178AC[15], NW_003871057.1:g.499178AC[17], NW_003871057.1:g.499178AC[18], NW_003871057.1:g.499178AC[19], NW_003871057.1:g.499178AC[20], NW_003871057.1:g.499178AC[21], NW_003871057.1:g.499178AC[22], NW_003871057.1:g.499178AC[23], NW_003871057.1:g.499178AC[24], NW_003871057.1:g.499178AC[25], NW_003871057.1:g.499178AC[26], NG_029062.2:g.5779AC[9], NG_029062.2:g.5779AC[10], NG_029062.2:g.5779AC[11], NG_029062.2:g.5779AC[12], NG_029062.2:g.5779AC[13], NG_029062.2:g.5779AC[14], NG_029062.2:g.5779AC[15], NG_029062.2:g.5779AC[17], NG_029062.2:g.5779AC[18], NG_029062.2:g.5779AC[19], NG_029062.2:g.5779AC[20], NG_029062.2:g.5779AC[21], NG_029062.2:g.5779AC[22], NG_029062.2:g.5779AC[23], NG_029062.2:g.5779AC[24], NG_029062.2:g.5779AC[25], NG_029062.2:g.5779AC[26], NC_000001.10:g.206681657AC[9], NC_000001.10:g.206681657AC[10], NC_000001.10:g.206681657AC[11], NC_000001.10:g.206681657AC[12], NC_000001.10:g.206681657AC[13], NC_000001.10:g.206681657AC[14], NC_000001.10:g.206681657AC[15], NC_000001.10:g.206681657AC[17], NC_000001.10:g.206681657AC[18], NC_000001.10:g.206681657AC[19], NC_000001.10:g.206681657AC[20], NC_000001.10:g.206681657AC[21], NC_000001.10:g.206681657AC[22], NC_000001.10:g.206681657AC[23], NC_000001.10:g.206681657AC[24], NC_000001.10:g.206681657AC[25], NC_000001.10:g.206681657AC[26]

Select item 14914322223.

rs1491432222 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 1:206553709 (GRCh38)
1:206727037 (GRCh37)
Canonical SPDI:: NC_000001.11:206553708:AG:
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000043/6 (GnomAD)
-=0.000053/14 (TOPMED)
HGVS:: NC_000001.11:g.206553709_206553710del, NW_003871057.1:g.544563_544564del, NG_029062.2:g.51164_51165del, NC_000001.10:g.206727037_206727038del

Select item 14914043554.

rs1491404355 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 1:206523444 (GRCh38)
1:206696777 (GRCh37)
Canonical SPDI:: NC_000001.11:206523437:TATATATA:TATATA
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATA=0.000184/3 (ALFA)
-=0.000264/28 (GnomAD)
-=0.002018/34 (TOMMO)
HGVS:: NC_000001.11:g.206523438TA[3], NW_003871057.1:g.514292TA[3], NG_029062.2:g.20893TA[3], NC_000001.10:g.206696771TA[3]

Select item 14913613025.

rs1491361302 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 1:206523916 (GRCh38)
1:206697249 (GRCh37)
Canonical SPDI:: NC_000001.11:206523915:AA:
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00001/1 (GnomAD)
HGVS:: NC_000001.11:g.206523916_206523917del, NW_003871057.1:g.514770_514771del, NG_029062.2:g.21371_21372del, NC_000001.10:g.206697249_206697250del

Select item 14912518426.

rs1491251842 has merged into rs1366334270 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>-,TATA [Show Flanks]
Chromosome:: 1:206523924 (GRCh38)
1:206697257 (GRCh37)
Canonical SPDI:: NC_000001.11:206523916:ATATATATA:ATATATA,NC_000001.11:206523916:ATATATATA:ATATATATATA
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: ATATATATATA=0./0 (ALFA)
-=0.00001/1 (GnomAD)
HGVS:: NC_000001.11:g.206523918TA[3], NC_000001.11:g.206523918TA[5], NW_003871057.1:g.514772TA[3], NW_003871057.1:g.514772TA[5], NG_029062.2:g.21373TA[3], NG_029062.2:g.21373TA[5], NC_000001.10:g.206697251TA[3], NC_000001.10:g.206697251TA[5]

Select item 14912217147.

rs1491221714 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TACA [Show Flanks]
Chromosome:: 1:206508323 (GRCh38)
1:206681657 (GRCh37)
Canonical SPDI:: NC_000001.11:206508323:ACA:ACATACA
Gene:: RASSF5 (Varview), LOC124904493 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: ACATACA=0./0 (ALFA)
ACAT=0.00002/1 (GnomAD)
HGVS:: NC_000001.11:g.206508326_206508327insTACA, NW_003871057.1:g.499180_499181insTACA, NG_029062.2:g.5781_5782insTACA, NC_000001.10:g.206681659_206681660insTACA

Select item 14911297598.

rs1491129759 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 1:206553709 (GRCh38)
1:206727038 (GRCh37)
Canonical SPDI:: NC_000001.11:206553709:GGGGG:GGGGGG
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: GGGGGG=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.206553714dup, NW_003871057.1:g.544568dup, NG_029062.2:g.51169dup, NC_000001.10:g.206727042dup

Select item 14910582939.

rs1491058293 has merged into rs201417256 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 1:206555367 (GRCh38)
1:206728695 (GRCh37)
Canonical SPDI:: NC_000001.11:206555365:TGT:T
Gene:: RASSF5 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000162/3 (ALFA)
-=0.000042/11 (TOPMED)
-=0.000076/10 (GnomAD)
-=0.000495/8 (TOMMO)
-=0.000678/3 (Estonian)
HGVS:: NC_000001.11:g.206555367_206555368del, NW_003871057.1:g.546221_546222del, NG_029062.2:g.52822_52823del, NC_000001.10:g.206728695_206728696del

Select item 149096524610.

rs1490965246 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 1:206524052 (GRCh38)
1:206697385 (GRCh37)
Canonical SPDI:: NC_000001.11:206524051:AA:
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00379/45 (ALFA)
HGVS:: NC_000001.11:g.206524052_206524053del, NW_003871057.1:g.514906_514907del, NG_029062.2:g.21507_21508del, NC_000001.10:g.206697385_206697386del

Select item 149093209111.

rs1490932091 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 1:206540256 (GRCh38)
1:206713586 (GRCh37)
Canonical SPDI:: NC_000001.11:206540256:AAAA:AAAAA
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAA=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.206540260dup, NW_003871057.1:g.531114dup, NG_029062.2:g.37715dup, NC_000001.10:g.206713589dup

Select item 149090294012.

rs1490902940 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:206556243 (GRCh38)
1:206729571 (GRCh37)
Canonical SPDI:: NC_000001.11:206556242:C:T
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.206556243C>T, NW_003871057.1:g.547097C>T, NG_029062.2:g.53698C>T, NC_000001.10:g.206729571C>T

Select item 149087297513.

rs1490872975 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:206557282 (GRCh38)
1:206730610 (GRCh37)
Canonical SPDI:: NC_000001.11:206557281:G:A
Gene:: RASSF5 (Varview), LOC124904494 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,5_prime_UTR_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.206557282G>A, NW_003871057.1:g.548136G>A, NG_029062.2:g.54737G>A, NM_182665.4:c.-292G>A, NM_182665.3:c.-292G>A, NM_182665.2:c.-292G>A, NC_000001.10:g.206730610G>A

Select item 149080589114.

rs1490805891 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:206548157 (GRCh38)
1:206721485 (GRCh37)
Canonical SPDI:: NC_000001.11:206548156:C:A,NC_000001.11:206548156:C:T
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_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_000001.11:g.206548157C>A, NC_000001.11:g.206548157C>T, NW_003871057.1:g.539011C>A, NW_003871057.1:g.539011C>T, NG_029062.2:g.45612C>A, NG_029062.2:g.45612C>T, NC_000001.10:g.206721485C>A, NC_000001.10:g.206721485C>T

Select item 149079374015.

rs1490793740 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:206564895 (GRCh38)
1:206738223 (GRCh37)
Canonical SPDI:: NC_000001.11:206564894:T:C
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.206564895T>C, NW_003871057.1:g.555749T>C, NG_029062.2:g.62350T>C, NC_000001.10:g.206738223T>C

Select item 149074914416.

rs1490749144 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:206508870 (GRCh38)
1:206682203 (GRCh37)
Canonical SPDI:: NC_000001.11:206508869:G:T
Gene:: RASSF5 (Varview), LOC124904493 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.206508870G>T, NW_003871057.1:g.499724G>T, NG_029062.2:g.6325G>T, NC_000001.10:g.206682203G>T

Select item 149070385517.

rs1490703855 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:206523697 (GRCh38)
1:206697030 (GRCh37)
Canonical SPDI:: NC_000001.11:206523696:A:T
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00001/1 (GnomAD)
A=0.5/1 (SGDP_PRJ)
HGVS:: NC_000001.11:g.206523697A>T, NW_003871057.1:g.514551A>T, NG_029062.2:g.21152A>T, NC_000001.10:g.206697030A>T

Select item 149069363418.

rs1490693634 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:206582465 (GRCh38)
1:206755797 (GRCh37)
Canonical SPDI:: NC_000001.11:206582464:G:A,NC_000001.11:206582464:G:T
Gene:: EIF2D (Varview), RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000036/5 (GnomAD)
HGVS:: NC_000001.11:g.206582465G>A, NC_000001.11:g.206582465G>T, NW_003871057.1:g.573319G>A, NW_003871057.1:g.573319G>T, NG_029062.2:g.79920G>A, NG_029062.2:g.79920G>T, NC_000001.10:g.206755797G>A, NC_000001.10:g.206755797G>T

Select item 149069082319.

rs1490690823 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:206523715 (GRCh38)
1:206697048 (GRCh37)
Canonical SPDI:: NC_000001.11:206523714:C:A,NC_000001.11:206523714:C:T
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.206523715C>A, NC_000001.11:g.206523715C>T, NW_003871057.1:g.514569C>A, NW_003871057.1:g.514569C>T, NG_029062.2:g.21170C>A, NG_029062.2:g.21170C>T, NC_000001.10:g.206697048C>A, NC_000001.10:g.206697048C>T

Select item 149064316720.

rs1490643167 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:206548685 (GRCh38)
1:206722013 (GRCh37)
Canonical SPDI:: NC_000001.11:206548684:C:G
Gene:: RASSF5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_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_000001.11:g.206548685C>G, NW_003871057.1:g.539539C>G, NG_029062.2:g.46140C>G, NC_000001.10:g.206722013C>G

<< First< Prev

Page of 50

Next >Last >>

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 1000

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity