SNP Links for Gene (Select 353345) - SNP

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Select item 14914628331.

rs1491462833 has merged into rs1176520782 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 7:37732151 (GRCh38)
7:37771753 (GRCh37)
Canonical SPDI:: NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:37732144:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: GPR141 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000007.14:g.37732151_37732161del, NC_000007.14:g.37732156_37732161del, NC_000007.14:g.37732158_37732161del, NC_000007.14:g.37732159_37732161del, NC_000007.14:g.37732160_37732161del, NC_000007.14:g.37732161del, NC_000007.14:g.37732161dup, NC_000007.14:g.37732160_37732161dup, NC_000007.14:g.37732159_37732161dup, NC_000007.14:g.37732158_37732161dup, NC_000007.14:g.37732157_37732161dup, NC_000007.14:g.37732156_37732161dup, NC_000007.14:g.37732155_37732161dup, NC_000007.14:g.37732154_37732161dup, NC_000007.14:g.37732153_37732161dup, NC_000007.14:g.37732145_37732161dup, NC_000007.14:g.37732161_37732162insTTTTTTTTTTTTTTTTTT, NC_000007.13:g.37771753_37771763del, NC_000007.13:g.37771758_37771763del, NC_000007.13:g.37771760_37771763del, NC_000007.13:g.37771761_37771763del, NC_000007.13:g.37771762_37771763del, NC_000007.13:g.37771763del, NC_000007.13:g.37771763dup, NC_000007.13:g.37771762_37771763dup, NC_000007.13:g.37771761_37771763dup, NC_000007.13:g.37771760_37771763dup, NC_000007.13:g.37771759_37771763dup, NC_000007.13:g.37771758_37771763dup, NC_000007.13:g.37771757_37771763dup, NC_000007.13:g.37771756_37771763dup, NC_000007.13:g.37771755_37771763dup, NC_000007.13:g.37771747_37771763dup, NC_000007.13:g.37771763_37771764insTTTTTTTTTTTTTTTTTT

Select item 14913460902.

rs1491346090 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 7:37733671 (GRCh38)
7:37773274 (GRCh37)
Canonical SPDI:: NC_000007.14:37733671::G
Gene:: GPR141 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000007.14:g.37733671_37733672insG, NC_000007.13:g.37773273_37773274insG

Select item 14913181733.

rs1491318173 has merged into rs146286812 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA [Show Flanks]
Chromosome:: 7:37722734 (GRCh38)
7:37762336 (GRCh37)
Canonical SPDI:: NC_000007.14:37722720:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000007.14:37722720:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000007.14:37722720:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000007.14:37722720:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000007.14:37722720:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000007.14:37722720:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000007.14:37722720:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000007.14:37722720:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37722720:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37722720:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA
Gene:: GPR141 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAA=0./0 (ALFA)
AA=0.379/1898 (1000Genomes)
HGVS:: NC_000007.14:g.37722734_37722738del, NC_000007.14:g.37722735_37722738del, NC_000007.14:g.37722736_37722738del, NC_000007.14:g.37722737_37722738del, NC_000007.14:g.37722738del, NC_000007.14:g.37722738dup, NC_000007.14:g.37722737_37722738dup, NC_000007.14:g.37722736_37722738dup, NC_000007.14:g.37722735_37722738dup, NC_000007.14:g.37722733_37722738dup, NC_000007.13:g.37762336_37762340del, NC_000007.13:g.37762337_37762340del, NC_000007.13:g.37762338_37762340del, NC_000007.13:g.37762339_37762340del, NC_000007.13:g.37762340del, NC_000007.13:g.37762340dup, NC_000007.13:g.37762339_37762340dup, NC_000007.13:g.37762338_37762340dup, NC_000007.13:g.37762337_37762340dup, NC_000007.13:g.37762335_37762340dup

Select item 14912488444.

rs1491248844 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 7:37733671 (GRCh38)
7:37773273 (GRCh37)
Canonical SPDI:: NC_000007.14:37733670:CA:
Gene:: GPR141 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00034/4 (ALFA)
HGVS:: NC_000007.14:g.37733671_37733672del, NC_000007.13:g.37773273_37773274del

Select item 14912270385.

rs1491227038 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->CA
Chromosome:: no mapping
Canonical SPDI:

Select item 14912205156.

rs1491220515 [Homo sapiens]

Variant type:: DEL
Alleles:: CC>- [Show Flanks]
Chromosome:: 7:37691287 (GRCh38)
7:37730889 (GRCh37)
Canonical SPDI:: NC_000007.14:37691286:CC:
Gene:: GPR141 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00248/183 (GnomAD)
-=0.00662/101 (TOMMO)
HGVS:: NC_000007.14:g.37691287_37691288del, NC_000007.13:g.37730889_37730890del

Select item 14910936657.

rs1491093665 has merged into rs66783277 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 7:37708322 (GRCh38)
7:37747924 (GRCh37)
Canonical SPDI:: NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:37708310:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: GPR141 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000007.14:g.37708322_37708335del, NC_000007.14:g.37708323_37708335del, NC_000007.14:g.37708324_37708335del, NC_000007.14:g.37708325_37708335del, NC_000007.14:g.37708326_37708335del, NC_000007.14:g.37708327_37708335del, NC_000007.14:g.37708328_37708335del, NC_000007.14:g.37708329_37708335del, NC_000007.14:g.37708330_37708335del, NC_000007.14:g.37708331_37708335del, NC_000007.14:g.37708332_37708335del, NC_000007.14:g.37708333_37708335del, NC_000007.14:g.37708334_37708335del, NC_000007.14:g.37708335del, NC_000007.14:g.37708335dup, NC_000007.14:g.37708334_37708335dup, NC_000007.14:g.37708333_37708335dup, NC_000007.14:g.37708332_37708335dup, NC_000007.14:g.37708331_37708335dup, NC_000007.14:g.37708330_37708335dup, NC_000007.14:g.37708327_37708335dup, NC_000007.14:g.37708326_37708335dup, NC_000007.14:g.37708325_37708335dup, NC_000007.14:g.37708324_37708335dup, NC_000007.14:g.37708323_37708335dup, NC_000007.14:g.37708322_37708335dup, NC_000007.14:g.37708321_37708335dup, NC_000007.14:g.37708320_37708335dup, NC_000007.14:g.37708319_37708335dup, NC_000007.14:g.37708318_37708335dup, NC_000007.14:g.37708315_37708335dup, NC_000007.14:g.37708335_37708336insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.13:g.37747924_37747937del, NC_000007.13:g.37747925_37747937del, NC_000007.13:g.37747926_37747937del, NC_000007.13:g.37747927_37747937del, NC_000007.13:g.37747928_37747937del, NC_000007.13:g.37747929_37747937del, NC_000007.13:g.37747930_37747937del, NC_000007.13:g.37747931_37747937del, NC_000007.13:g.37747932_37747937del, NC_000007.13:g.37747933_37747937del, NC_000007.13:g.37747934_37747937del, NC_000007.13:g.37747935_37747937del, NC_000007.13:g.37747936_37747937del, NC_000007.13:g.37747937del, NC_000007.13:g.37747937dup, NC_000007.13:g.37747936_37747937dup, NC_000007.13:g.37747935_37747937dup, NC_000007.13:g.37747934_37747937dup, NC_000007.13:g.37747933_37747937dup, NC_000007.13:g.37747932_37747937dup, NC_000007.13:g.37747929_37747937dup, NC_000007.13:g.37747928_37747937dup, NC_000007.13:g.37747927_37747937dup, NC_000007.13:g.37747926_37747937dup, NC_000007.13:g.37747925_37747937dup, NC_000007.13:g.37747924_37747937dup, NC_000007.13:g.37747923_37747937dup, NC_000007.13:g.37747922_37747937dup, NC_000007.13:g.37747921_37747937dup, NC_000007.13:g.37747920_37747937dup, NC_000007.13:g.37747917_37747937dup, NC_000007.13:g.37747937_37747938insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14910738088.

rs1491073808 has merged into rs11323927 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 7:37722437 (GRCh38)
7:37762039 (GRCh37)
Canonical SPDI:: NC_000007.14:37722426:AAAAAAAAAAAAAA:AAAAAAAAAA,NC_000007.14:37722426:AAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000007.14:37722426:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000007.14:37722426:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000007.14:37722426:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000007.14:37722426:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000007.14:37722426:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000007.14:37722426:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA
Gene:: GPR141 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.3952/1979 (1000Genomes)
HGVS:: NC_000007.14:g.37722437_37722440del, NC_000007.14:g.37722438_37722440del, NC_000007.14:g.37722439_37722440del, NC_000007.14:g.37722440del, NC_000007.14:g.37722440dup, NC_000007.14:g.37722439_37722440dup, NC_000007.14:g.37722438_37722440dup, NC_000007.14:g.37722431_37722440dup, NC_000007.13:g.37762039_37762042del, NC_000007.13:g.37762040_37762042del, NC_000007.13:g.37762041_37762042del, NC_000007.13:g.37762042del, NC_000007.13:g.37762042dup, NC_000007.13:g.37762041_37762042dup, NC_000007.13:g.37762040_37762042dup, NC_000007.13:g.37762033_37762042dup

Select item 14909922239.

rs1490992223 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:37689509 (GRCh38)
7:37729111 (GRCh37)
Canonical SPDI:: NC_000007.14:37689508:T:A
Gene:: GPR141 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.37689509T>A, NC_000007.13:g.37729111T>A

Select item 149095208210.

rs1490952082 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 7:37684831 (GRCh38)
7:37724434 (GRCh37)
Canonical SPDI:: NC_000007.14:37684830:A:T
Gene:: GPR141 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000029/4 (GnomAD)
T=0.000034/9 (TOPMED)
HGVS:: NC_000007.14:g.37684831A>T, NC_000007.13:g.37724434A>T

Select item 149093385811.

rs1490933858 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:37706870 (GRCh38)
7:37746472 (GRCh37)
Canonical SPDI:: NC_000007.14:37706869:G:T
Gene:: GPR141 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.37706870G>T, NC_000007.13:g.37746472G>T

Select item 149092642512.

rs1490926425 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:37682034 (GRCh38)
7:37721637 (GRCh37)
Canonical SPDI:: NC_000007.14:37682033:G:T
Gene:: GPR141 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000066/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000007.14:g.37682034G>T, NC_000007.13:g.37721637G>T

Select item 149085674113.

rs1490856741 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:37724122 (GRCh38)
7:37763724 (GRCh37)
Canonical SPDI:: NC_000007.14:37724121:A:G
Gene:: GPR141 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000007.14:g.37724122A>G, NC_000007.13:g.37763724A>G, XM_011515385.3:c.-5077A>G, XM_011515385.2:c.-5077A>G

Select item 149074933614.

rs1490749336 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:37697326 (GRCh38)
7:37736928 (GRCh37)
Canonical SPDI:: NC_000007.14:37697325:A:G
Gene:: GPR141 (Varview)
Functional Consequence:: 5_prime_UTR_variant,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_000007.14:g.37697326A>G, NC_000007.13:g.37736928A>G, XM_017012163.3:c.-841A>G, XM_017012163.2:c.-841A>G, XM_017012163.1:c.-841A>G, XM_047420330.1:c.-841A>G, XM_047420332.1:c.-893A>G

Select item 149074610815.

rs1490746108 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 7:37705182 (GRCh38)
7:37744784 (GRCh37)
Canonical SPDI:: NC_000007.14:37705181:C:G
Gene:: GPR141 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.37705182C>G, NC_000007.13:g.37744784C>G

Select item 149063416816.

rs1490634168 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:37737223 (GRCh38)
7:37776825 (GRCh37)
Canonical SPDI:: NC_000007.14:37737222:T:C
Gene:: GPR141 (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.37737223T>C, NC_000007.13:g.37776825T>C

Select item 149060702217.

rs1490607022 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:37721719 (GRCh38)
7:37761321 (GRCh37)
Canonical SPDI:: NC_000007.14:37721718:A:G
Gene:: GPR141 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000007.14:g.37721719A>G, NC_000007.13:g.37761321A>G

Select item 149057912918.

rs1490579129 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:37738213 (GRCh38)
7:37777815 (GRCh37)
Canonical SPDI:: NC_000007.14:37738212:A:G
Gene:: GPR141 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000007.14:g.37738213A>G, NC_000007.13:g.37777815A>G

Select item 149050269719.

rs1490502697 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:37690077 (GRCh38)
7:37729679 (GRCh37)
Canonical SPDI:: NC_000007.14:37690076:T:C
Gene:: GPR141 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.37690077T>C, NC_000007.13:g.37729679T>C

Select item 149045118820.

rs1490451188 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:37743469 (GRCh38)
7:37783071 (GRCh37)
Canonical SPDI:: NC_000007.14:37743468:C:T
Gene:: GPR141 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000007.14:g.37743469C>T, NC_000007.13:g.37783071C>T, XM_011515374.4:c.*2158C>T, XM_011515374.3:c.*2158C>T, XM_011515374.2:c.*2158C>T, XM_011515375.4:c.*2158C>T, XM_011515375.3:c.*2158C>T, XM_011515375.2:c.*2158C>T, XM_011515383.4:c.*2158C>T, XM_011515383.3:c.*2158C>T, XM_011515383.2:c.*2158C>T, XM_011515385.3:c.*2158C>T, XM_011515385.2:c.*2158C>T, XM_017012163.3:c.*2158C>T, XM_017012163.2:c.*2158C>T, XM_017012163.1:c.*2158C>T, NM_181791.3:c.*2158C>T, NM_181791.2:c.*2158C>T, XM_011515386.3:c.*2158C>T, XM_011515386.2:c.*2158C>T, XM_011515389.3:c.*2158C>T, XM_011515389.2:c.*2158C>T, XM_011515388.3:c.*2158C>T, XM_011515388.2:c.*2158C>T, NM_001329993.2:c.*2158C>T, NM_001329993.1:c.*2158C>T, NM_001329994.2:c.*2158C>T, NM_001329994.1:c.*2158C>T, XM_047420330.1:c.*2158C>T, XM_047420332.1:c.*2158C>T, NM_001381946.1:c.*2158C>T, XM_047420331.1:c.*2158C>T

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