SNP Links for Gene (Select 345051) - SNP

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Items: 1 to 20 of 4413

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Select item 14909171641.

rs1490917164 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:146223366 (GRCh38)
4:147144518 (GRCh37)
Canonical SPDI:: NC_000004.12:146223365:C:G
Gene:: REELD1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.146223366C>G, NC_000004.11:g.147144518C>G, NG_083499.1:g.1383C>G

Select item 14908132442.

rs1490813244 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:146228376 (GRCh38)
4:147149528 (GRCh37)
Canonical SPDI:: NC_000004.12:146228375:C:T
Gene:: REELD1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.146228376C>T, NC_000004.11:g.147149528C>T, NM_001354631.1:c.762C>T, NM_001371071.1:c.762C>T

Select item 14905727743.

rs1490572774 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:146214281 (GRCh38)
4:147135433 (GRCh37)
Canonical SPDI:: NC_000004.12:146214280:T:A
Gene:: REELD1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.146214281T>A, NC_000004.11:g.147135433T>A

Select item 14905381094.

rs1490538109 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 4:146215289 (GRCh38)
4:147136441 (GRCh37)
Canonical SPDI:: NC_000004.12:146215288:G:A,NC_000004.12:146215288:G:C
Gene:: REELD1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
A=0.000071/2 (TOMMO)
HGVS:: NC_000004.12:g.146215289G>A, NC_000004.12:g.146215289G>C, NC_000004.11:g.147136441G>A, NC_000004.11:g.147136441G>C

Select item 14904523015.

rs1490452301 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:146221928 (GRCh38)
4:147143080 (GRCh37)
Canonical SPDI:: NC_000004.12:146221927:C:A
Gene:: REELD1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000004.12:g.146221928C>A, NC_000004.11:g.147143080C>A

Select item 14903032806.

rs1490303280 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:146230683 (GRCh38)
4:147151835 (GRCh37)
Canonical SPDI:: NC_000004.12:146230682:T:C
Gene:: REELD1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.146230683T>C, NC_000004.11:g.147151835T>C, NM_001354631.1:c.*170T>C, NM_001371071.1:c.*170T>C

Select item 14902777067.

rs1490277706 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:146230061 (GRCh38)
4:147151213 (GRCh37)
Canonical SPDI:: NC_000004.12:146230060:G:A
Gene:: REELD1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.146230061G>A, NC_000004.11:g.147151213G>A, NM_001354631.1:c.1129G>A, NM_001371071.1:c.1129G>A, NP_001341560.1:p.Gly377Arg, NP_001358000.1:p.Gly377Arg

Select item 14900273458.

rs1490027345 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:146229887 (GRCh38)
4:147151039 (GRCh37)
Canonical SPDI:: NC_000004.12:146229886:T:C
Gene:: REELD1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.146229887T>C, NC_000004.11:g.147151039T>C

Select item 14899598089.

rs1489959808 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AT [Show Flanks]
Chromosome:: 4:146221520 (GRCh38)
4:147142673 (GRCh37)
Canonical SPDI:: NC_000004.12:146221520:ATAT:ATATAT
Gene:: REELD1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: ATATAT=0./0 (ALFA)
AT=0.000026/7 (TOPMED)
HGVS:: NC_000004.12:g.146221521AT[3], NC_000004.11:g.147142673AT[3]

Select item 148980135310.

rs1489801353 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:146231446 (GRCh38)
4:147152598 (GRCh37)
Canonical SPDI:: NC_000004.12:146231445:A:T
Gene:: REELD1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.146231446A>T, NC_000004.11:g.147152598A>T, NM_001354631.1:c.*933A>T, NM_001371071.1:c.*933A>T

Select item 148960166911.

rs1489601669 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTATAACAA>- [Show Flanks]
Chromosome:: 4:146227169 (GRCh38)
4:147148321 (GRCh37)
Canonical SPDI:: NC_000004.12:146227163:AACAACTATAACAA:AACAA
Gene:: REELD1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000004.12:g.146227169_146227177del, NC_000004.11:g.147148321_147148329del

Select item 148956815812.

rs1489568158 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:146224404 (GRCh38)
4:147145556 (GRCh37)
Canonical SPDI:: NC_000004.12:146224403:A:C
Gene:: REELD1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.146224404A>C, NC_000004.11:g.147145556A>C

Select item 148938292913.

rs1489382929 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:146217665 (GRCh38)
4:147138817 (GRCh37)
Canonical SPDI:: NC_000004.12:146217664:A:G
Gene:: REELD1 (Varview)
Functional Consequence:: intron_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_000004.12:g.146217665A>G, NC_000004.11:g.147138817A>G

Select item 148926134014.

rs1489261340 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:146216933 (GRCh38)
4:147138085 (GRCh37)
Canonical SPDI:: NC_000004.12:146216932:A:T
Gene:: REELD1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
HGVS:: NC_000004.12:g.146216933A>T, NC_000004.11:g.147138085A>T

Select item 148924867315.

rs1489248673 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:146219995 (GRCh38)
4:147141147 (GRCh37)
Canonical SPDI:: NC_000004.12:146219994:G:A
Gene:: REELD1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000004.12:g.146219995G>A, NC_000004.11:g.147141147G>A

Select item 148912955116.

rs1489129551 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 4:146231143 (GRCh38)
4:147152295 (GRCh37)
Canonical SPDI:: NC_000004.12:146231142:G:A,NC_000004.12:146231142:G:T
Gene:: REELD1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.00004/1 (TOMMO)
A=0.00034/1 (KOREAN)
HGVS:: NC_000004.12:g.146231143G>A, NC_000004.12:g.146231143G>T, NC_000004.11:g.147152295G>A, NC_000004.11:g.147152295G>T, NM_001354631.1:c.*630G>A, NM_001354631.1:c.*630G>T, NM_001371071.1:c.*630G>A, NM_001371071.1:c.*630G>T

Select item 148912660917.

rs1489126609 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:146224928 (GRCh38)
4:147146080 (GRCh37)
Canonical SPDI:: NC_000004.12:146224927:C:A
Gene:: REELD1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000004.12:g.146224928C>A, NC_000004.11:g.147146080C>A

Select item 148895638618.

rs1488956386 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:146213231 (GRCh38)
4:147134383 (GRCh37)
Canonical SPDI:: NC_000004.12:146213230:C:T
Gene:: REELD1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.146213231C>T, NC_000004.11:g.147134383C>T

Select item 148892360319.

rs1488923603 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 4:146228031 (GRCh38)
4:147149183 (GRCh37)
Canonical SPDI:: NC_000004.12:146228030:G:A,NC_000004.12:146228030:G:T
Gene:: REELD1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000004.12:g.146228031G>A, NC_000004.12:g.146228031G>T, NC_000004.11:g.147149183G>A, NC_000004.11:g.147149183G>T

Select item 148858563220.

rs1488585632 [Homo sapiens]

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

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