SNP Links for Nucleotide (Select 304307765) - SNP

Links from Nucleotide

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Select item 14906280611.

rs1490628061 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:39030611 (GRCh38)
17:37186864 (GRCh37)
Canonical SPDI:: NC_000017.11:39030610:T:C
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.39030611T>C, NC_000017.10:g.37186864T>C, NR_033753.2:n.706T>C, NM_198502.1:c.-826T>C

Select item 14906125842.

rs1490612584 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 17:39031872 (GRCh38)
17:37188125 (GRCh37)
Canonical SPDI:: NC_000017.11:39031871:CC:C
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000011/3 (TOPMED)
HGVS:: NC_000017.11:g.39031873del, NC_000017.10:g.37188126del, NR_033753.2:n.1968del, NM_198502.1:c.437del

Select item 14895039293.

rs1489503929 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 17:39031762 (GRCh38)
17:37188015 (GRCh37)
Canonical SPDI:: NC_000017.11:39031761:T:A,NC_000017.11:39031761:T:C
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.39031762T>A, NC_000017.11:g.39031762T>C, NC_000017.10:g.37188015T>A, NC_000017.10:g.37188015T>C, NR_033753.2:n.1857T>A, NR_033753.2:n.1857T>C, NM_198502.1:c.326T>A, NM_198502.1:c.326T>C

Select item 14887525064.

rs1488752506 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 17:39031665 (GRCh38)
17:37187918 (GRCh37)
Canonical SPDI:: NC_000017.11:39031664:G:A,NC_000017.11:39031664:G:T
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
HGVS:: NC_000017.11:g.39031665G>A, NC_000017.11:g.39031665G>T, NC_000017.10:g.37187918G>A, NC_000017.10:g.37187918G>T, NR_033753.2:n.1760G>A, NR_033753.2:n.1760G>T, NM_198502.1:c.229G>A, NM_198502.1:c.229G>T

Select item 14881207585.

rs1488120758 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 17:39030188 (GRCh38)
17:37186441 (GRCh37)
Canonical SPDI:: NC_000017.11:39030187:A:T
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000017.11:g.39030188A>T, NC_000017.10:g.37186441A>T, NR_033753.2:n.283A>T, NM_198502.1:c.-1248A>T

Select item 14878609796.

rs1487860979 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 17:39031199 (GRCh38)
17:37187452 (GRCh37)
Canonical SPDI:: NC_000017.11:39031198:T:A
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.39031199T>A, NC_000017.10:g.37187452T>A, NR_033753.2:n.1294T>A, NM_198502.1:c.-238T>A

Select item 14846378937.

rs1484637893 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 17:39030607 (GRCh38)
17:37186860 (GRCh37)
Canonical SPDI:: NC_000017.11:39030606:C:A
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000017.11:g.39030607C>A, NC_000017.10:g.37186860C>A, NR_033753.2:n.702C>A, NM_198502.1:c.-830C>A

Select item 14838217778.

rs1483821777 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:39030928 (GRCh38)
17:37187181 (GRCh37)
Canonical SPDI:: NC_000017.11:39030927:G:C
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.39030928G>C, NC_000017.10:g.37187181G>C, NR_033753.2:n.1023G>C, NM_198502.1:c.-509G>C

Select item 14837004129.

rs1483700412 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:39043261 (GRCh38)
17:37199514 (GRCh37)
Canonical SPDI:: NC_000017.11:39043260:T:C
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.39043261T>C, NC_000017.10:g.37199514T>C, NR_033753.2:n.2667T>C, NM_198502.1:c.*182T>C

Select item 148289703510.

rs1482897035 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:39044548 (GRCh38)
17:37200801 (GRCh37)
Canonical SPDI:: NC_000017.11:39044547:G:A
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000017.11:g.39044548G>A, NC_000017.10:g.37200801G>A, NR_033753.2:n.2846G>A, NM_198502.1:c.*361G>A

Select item 148278030711.

rs1482780307 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 17:39044425 (GRCh38)
17:37200678 (GRCh37)
Canonical SPDI:: NC_000017.11:39044424:T:A
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000026/7 (TOPMED)
HGVS:: NC_000017.11:g.39044425T>A, NC_000017.10:g.37200678T>A, NR_033753.2:n.2723T>A, NM_198502.1:c.*238T>A

Select item 148130543912.

rs1481305439 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:39044651 (GRCh38)
17:37200904 (GRCh37)
Canonical SPDI:: NC_000017.11:39044650:C:T
Gene:: LRRC37A11P (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_000017.11:g.39044651C>T, NC_000017.10:g.37200904C>T, NR_033753.2:n.2949C>T, NM_198502.1:c.*464C>T

Select item 148099358313.

rs1480993583 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:39031997 (GRCh38)
17:37188250 (GRCh37)
Canonical SPDI:: NC_000017.11:39031996:G:A
Gene:: LRRC37A11P (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_000017.11:g.39031997G>A, NC_000017.10:g.37188250G>A, NR_033753.2:n.2092G>A, NM_198502.1:c.561G>A

Select item 147925473514.

rs1479254735 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:39030257 (GRCh38)
17:37186510 (GRCh37)
Canonical SPDI:: NC_000017.11:39030256:C:T
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.39030257C>T, NC_000017.10:g.37186510C>T, NR_033753.2:n.352C>T, NM_198502.1:c.-1179C>T

Select item 147739527815.

rs1477395278 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:39032380 (GRCh38)
17:37188633 (GRCh37)
Canonical SPDI:: NC_000017.11:39032379:G:A
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000017.11:g.39032380G>A, NC_000017.10:g.37188633G>A, NR_033753.2:n.2475G>A, NM_198502.1:c.944G>A

Select item 147733478816.

rs1477334788 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 17:39031448 (GRCh38)
17:37187701 (GRCh37)
Canonical SPDI:: NC_000017.11:39031447:C:A,NC_000017.11:39031447:C:T
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000017.11:g.39031448C>A, NC_000017.11:g.39031448C>T, NC_000017.10:g.37187701C>A, NC_000017.10:g.37187701C>T, NR_033753.2:n.1543C>A, NR_033753.2:n.1543C>T, NM_198502.1:c.12C>A, NM_198502.1:c.12C>T

Select item 147726284517.

rs1477262845 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:39031298 (GRCh38)
17:37187551 (GRCh37)
Canonical SPDI:: NC_000017.11:39031297:A:G
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.39031298A>G, NC_000017.10:g.37187551A>G, NR_033753.2:n.1393A>G, NM_198502.1:c.-139A>G

Select item 147601409518.

rs1476014095 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:39030017 (GRCh38)
17:37186270 (GRCh37)
Canonical SPDI:: NC_000017.11:39030016:C:T
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.39030017C>T, NC_000017.10:g.37186270C>T, NR_033753.2:n.112C>T, NM_198502.1:c.-1419C>T

Select item 147532545619.

rs1475325456 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 17:39044544 (GRCh38)
17:37200797 (GRCh37)
Canonical SPDI:: NC_000017.11:39044543:G:A,NC_000017.11:39044543:G:C
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000021/3 (GnomAD)
HGVS:: NC_000017.11:g.39044544G>A, NC_000017.11:g.39044544G>C, NC_000017.10:g.37200797G>A, NC_000017.10:g.37200797G>C, NR_033753.2:n.2842G>A, NR_033753.2:n.2842G>C, NM_198502.1:c.*357G>A, NM_198502.1:c.*357G>C

Select item 147482757520.

rs1474827575 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:39030124 (GRCh38)
17:37186377 (GRCh37)
Canonical SPDI:: NC_000017.11:39030123:G:T
Gene:: LRRC37A11P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.39030124G>T, NC_000017.10:g.37186377G>T, NR_033753.2:n.219G>T, NM_198502.1:c.-1312G>T

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