SNP Links for Nucleotide (Select 219521895) - SNP

Links from Nucleotide

Items: 1 to 20 of 433

<< First< Prev

Page of 22

Next >Last >>

Select item 14908787771.

rs1490878777 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:79827485 (GRCh38)
4:80748639 (GRCh37)
Canonical SPDI:: NC_000004.12:79827484:A:G
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.79827485A>G, NC_000004.11:g.80748639A>G, NM_058168.2:c.-23A>G, NR_026555.1:n.15A>G

Select item 14888919992.

rs1488891999 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 4:79862766 (GRCh38)
4:80783920 (GRCh37)
Canonical SPDI:: NC_000004.12:79862765:G:A,NC_000004.12:79862765:G:C
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000049/13 (TOPMED)
HGVS:: NC_000004.12:g.79862766G>A, NC_000004.12:g.79862766G>C, NC_000004.11:g.80783920G>A, NC_000004.11:g.80783920G>C, NR_026555.1:n.1610G>A, NR_026555.1:n.1610G>C

Select item 14858894913.

rs1485889491 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 4:79862173 (GRCh38)
4:80783327 (GRCh37)
Canonical SPDI:: NC_000004.12:79862172:TT:
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000004.12:g.79862173_79862174del, NC_000004.11:g.80783327_80783328del, NR_026555.1:n.1017_1018del

Select item 14816139494.

rs1481613949 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:79862055 (GRCh38)
4:80783209 (GRCh37)
Canonical SPDI:: NC_000004.12:79862054:A:G
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
G=0.000029/4 (GnomAD)
HGVS:: NC_000004.12:g.79862055A>G, NC_000004.11:g.80783209A>G, NR_026555.1:n.899A>G

Select item 14809686175.

rs1480968617 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 4:79827569 (GRCh38)
4:80748723 (GRCh37)
Canonical SPDI:: NC_000004.12:79827568:T:G
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.79827569T>G, NC_000004.11:g.80748723T>G, NM_058168.2:c.62T>G, NR_026555.1:n.99T>G

Select item 14777029246.

rs1477702924 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:79861936 (GRCh38)
4:80783090 (GRCh37)
Canonical SPDI:: NC_000004.12:79861935:A:C
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.79861936A>C, NC_000004.11:g.80783090A>C, NR_026555.1:n.780A>C

Select item 14773835837.

rs1477383583 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:79862427 (GRCh38)
4:80783581 (GRCh37)
Canonical SPDI:: NC_000004.12:79862426:C:T
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.79862427C>T, NC_000004.11:g.80783581C>T, NR_026555.1:n.1271C>T

Select item 14773419028.

rs1477341902 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:79861320 (GRCh38)
4:80782474 (GRCh37)
Canonical SPDI:: NC_000004.12:79861319:G:A
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_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_000004.12:g.79861320G>A, NC_000004.11:g.80782474G>A, NM_058168.2:c.*22G>A, NR_026555.1:n.164G>A

Select item 14763521979.

rs1476352197 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:79861789 (GRCh38)
4:80782943 (GRCh37)
Canonical SPDI:: NC_000004.12:79861788:T:C
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.79861789T>C, NC_000004.11:g.80782943T>C, NR_026555.1:n.633T>C

Select item 147537863810.

rs1475378638 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:79862256 (GRCh38)
4:80783410 (GRCh37)
Canonical SPDI:: NC_000004.12:79862255:A:G
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000004.12:g.79862256A>G, NC_000004.11:g.80783410A>G, NR_026555.1:n.1100A>G

Select item 147479090211.

rs1474790902 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:79861546 (GRCh38)
4:80782700 (GRCh37)
Canonical SPDI:: NC_000004.12:79861545:A:G
Gene:: PCAT4 (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=0.000011/3 (TOPMED)
HGVS:: NC_000004.12:g.79861546A>G, NC_000004.11:g.80782700A>G, NM_058168.2:c.*248A>G, NR_026555.1:n.390A>G

Select item 147311800512.

rs1473118005 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 4:79827530 (GRCh38)
4:80748684 (GRCh37)
Canonical SPDI:: NC_000004.12:79827529:G:A,NC_000004.12:79827529:G:T
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000004.12:g.79827530G>A, NC_000004.12:g.79827530G>T, NC_000004.11:g.80748684G>A, NC_000004.11:g.80748684G>T, NM_058168.2:c.23G>A, NM_058168.2:c.23G>T, NR_026555.1:n.60G>A, NR_026555.1:n.60G>T

Select item 147206263013.

rs1472062630 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:79862186 (GRCh38)
4:80783340 (GRCh37)
Canonical SPDI:: NC_000004.12:79862185:G:T
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000004.12:g.79862186G>T, NC_000004.11:g.80783340G>T, NR_026555.1:n.1030G>T

Select item 146845341114.

rs1468453411 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:79861976 (GRCh38)
4:80783130 (GRCh37)
Canonical SPDI:: NC_000004.12:79861975:G:A
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_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_000004.12:g.79861976G>A, NC_000004.11:g.80783130G>A, NR_026555.1:n.820G>A

Select item 146502279615.

rs1465022796 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:79861417 (GRCh38)
4:80782571 (GRCh37)
Canonical SPDI:: NC_000004.12:79861416:T:C
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000045/12 (TOPMED)
HGVS:: NC_000004.12:g.79861417T>C, NC_000004.11:g.80782571T>C, NM_058168.2:c.*119T>C, NR_026555.1:n.261T>C

Select item 146346227216.

rs1463462272 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:79861905 (GRCh38)
4:80783059 (GRCh37)
Canonical SPDI:: NC_000004.12:79861904:C:G
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.79861905C>G, NC_000004.11:g.80783059C>G, NR_026555.1:n.749C>G

Select item 146031966417.

rs1460319664 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:79863066 (GRCh38)
4:80784220 (GRCh37)
Canonical SPDI:: NC_000004.12:79863065:A:T
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.79863066A>T, NC_000004.11:g.80784220A>T, NR_026555.1:n.1910A>T

Select item 145851415918.

rs1458514159 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 4:79861310 (GRCh38)
4:80782464 (GRCh37)
Canonical SPDI:: NC_000004.12:79861309:A:C,NC_000004.12:79861309:A:T
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.79861310A>C, NC_000004.12:g.79861310A>T, NC_000004.11:g.80782464A>C, NC_000004.11:g.80782464A>T, NM_058168.2:c.*12A>C, NM_058168.2:c.*12A>T, NR_026555.1:n.154A>C, NR_026555.1:n.154A>T

Select item 145769561119.

rs1457695611 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>- [Show Flanks]
Chromosome:: 4:79861493 (GRCh38)
4:80782647 (GRCh37)
Canonical SPDI:: NC_000004.12:79861491:TTT:T
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.79861493_79861494del, NC_000004.11:g.80782647_80782648del, NM_058168.2:c.*195_*196del, NR_026555.1:n.337_338del

Select item 145635763220.

rs1456357632 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:79861953 (GRCh38)
4:80783107 (GRCh37)
Canonical SPDI:: NC_000004.12:79861952:A:T
Gene:: PCAT4 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.79861953A>T, NC_000004.11:g.80783107A>T, NR_026555.1:n.797A>T

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 433

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity