SNP Links for Protein (Select 8394456) - SNP

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Links from Protein

Items: 1 to 20 of 1000

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Select item 14909304351.

rs1490930435 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 3:52223653 (GRCh38)
3:52257669 (GRCh37)
Canonical SPDI:: NC_000003.12:52223652:G:A,NC_000003.12:52223652:G:C,NC_000003.12:52223652:G:T
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.52223653G>A, NC_000003.12:g.52223653G>C, NC_000003.12:g.52223653G>T, NC_000003.11:g.52257669G>A, NC_000003.11:g.52257669G>C, NC_000003.11:g.52257669G>T, NG_033933.1:g.7511C>T, NG_033933.1:g.7511C>G, NG_033933.1:g.7511C>A, NM_017442.4:c.663C>T, NM_017442.4:c.663C>G, NM_017442.4:c.663C>A, NM_017442.3:c.663C>T, NM_017442.3:c.663C>G, NM_017442.3:c.663C>A, NM_138688.1:c.492C>T, NM_138688.1:c.492C>G, NM_138688.1:c.492C>A, NP_059138.1:p.Ser221Arg, NP_059138.1:p.Ser221Arg

Select item 14897795452.

rs1489779545 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52223306 (GRCh38)
3:52257322 (GRCh37)
Canonical SPDI:: NC_000003.12:52223305:C:T
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: T=0./0 (KOREAN)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.52223306C>T, NC_000003.11:g.52257322C>T, NG_033933.1:g.7858G>A, NM_017442.4:c.1010G>A, NM_017442.3:c.1010G>A, NM_138688.1:c.839G>A, NP_059138.1:p.Arg337His

Select item 14885519833.

rs1488551983 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 3:52223244 (GRCh38)
3:52257260 (GRCh37)
Canonical SPDI:: NC_000003.12:52223243:G:C
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.52223244G>C, NC_000003.11:g.52257260G>C, NG_033933.1:g.7920C>G, NM_017442.4:c.1072C>G, NM_017442.3:c.1072C>G, NM_138688.1:c.901C>G, NP_059138.1:p.Pro358Ala

Select item 14882284924.

rs1488228492 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:52222779 (GRCh38)
3:52256795 (GRCh37)
Canonical SPDI:: NC_000003.12:52222778:T:C
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000003.12:g.52222779T>C, NC_000003.11:g.52256795T>C, NG_033933.1:g.8385A>G, NM_017442.4:c.1537A>G, NM_017442.3:c.1537A>G, NM_138688.1:c.1366A>G, NP_059138.1:p.Asn513Asp

Select item 14881670285.

rs1488167028 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:52221751 (GRCh38)
3:52255767 (GRCh37)
Canonical SPDI:: NC_000003.12:52221750:G:T
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.52221751G>T, NC_000003.11:g.52255767G>T, NG_033933.1:g.9413C>A, NM_017442.4:c.2565C>A, NM_017442.3:c.2565C>A, NM_138688.1:c.2394C>A

Select item 14874859116.

rs1487485911 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 3:52224280 (GRCh38)
3:52258296 (GRCh37)
Canonical SPDI:: NC_000003.12:52224279:A:T
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0.000031/1 (ALFA)
T=0.000009/2 (GnomAD_exomes)
HGVS:: NC_000003.12:g.52224280A>T, NC_000003.11:g.52258296A>T, NG_033933.1:g.6884T>A, NM_017442.4:c.36T>A, NM_017442.3:c.36T>A

Select item 14865892547.

rs1486589254 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52222263 (GRCh38)
3:52256279 (GRCh37)
Canonical SPDI:: NC_000003.12:52222262:C:T
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000003.12:g.52222263C>T, NC_000003.11:g.52256279C>T, NG_033933.1:g.8901G>A, NM_017442.4:c.2053G>A, NM_017442.3:c.2053G>A, NM_138688.1:c.1882G>A, NP_059138.1:p.Ala685Thr

Select item 14865293888.

rs1486529388 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 3:52221343 (GRCh38)
3:52255359 (GRCh37)
Canonical SPDI:: NC_000003.12:52221342:A:G,NC_000003.12:52221342:A:T
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
G=0.000009/1 (ExAC)
HGVS:: NC_000003.12:g.52221343A>G, NC_000003.12:g.52221343A>T, NC_000003.11:g.52255359A>G, NC_000003.11:g.52255359A>T, NG_033933.1:g.9821T>C, NG_033933.1:g.9821T>A, NM_017442.4:c.2973T>C, NM_017442.4:c.2973T>A, NM_017442.3:c.2973T>C, NM_017442.3:c.2973T>A, NM_138688.1:c.2802T>C, NM_138688.1:c.2802T>A, NP_059138.1:p.Ser991Arg

Select item 14858889899.

rs1485888989 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:52223197 (GRCh38)
3:52257213 (GRCh37)
Canonical SPDI:: NC_000003.12:52223196:G:T
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0.00005/1 (ALFA)
HGVS:: NC_000003.12:g.52223197G>T, NC_000003.11:g.52257213G>T, NG_033933.1:g.7967C>A, NM_017442.4:c.1119C>A, NM_017442.3:c.1119C>A, NM_138688.1:c.948C>A

Select item 148299694010.

rs1482996940 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52223535 (GRCh38)
3:52257551 (GRCh37)
Canonical SPDI:: NC_000003.12:52223534:C:T
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000003.12:g.52223535C>T, NC_000003.11:g.52257551C>T, NG_033933.1:g.7629G>A, NM_017442.4:c.781G>A, NM_017442.3:c.781G>A, NM_138688.1:c.610G>A, NP_059138.1:p.Ala261Thr

Select item 148179140411.

rs1481791404 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:52222442 (GRCh38)
3:52256458 (GRCh37)
Canonical SPDI:: NC_000003.12:52222441:T:C
Gene:: TLR9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.52222442T>C, NC_000003.11:g.52256458T>C, NG_033933.1:g.8722A>G, NM_017442.4:c.1874A>G, NM_017442.3:c.1874A>G, NM_138688.1:c.1703A>G, NP_059138.1:p.Gln625Arg

Select item 148165503312.

rs1481655033 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52221869 (GRCh38)
3:52255885 (GRCh37)
Canonical SPDI:: NC_000003.12:52221868:C:T
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.52221869C>T, NC_000003.11:g.52255885C>T, NG_033933.1:g.9295G>A, NM_017442.4:c.2447G>A, NM_017442.3:c.2447G>A, NM_138688.1:c.2276G>A, NP_059138.1:p.Trp816Ter

Select item 148165063113.

rs1481650631 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:52223593 (GRCh38)
3:52257609 (GRCh37)
Canonical SPDI:: NC_000003.12:52223592:G:A
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000003.12:g.52223593G>A, NC_000003.11:g.52257609G>A, NG_033933.1:g.7571C>T, NM_017442.4:c.723C>T, NM_017442.3:c.723C>T, NM_138688.1:c.552C>T

Select item 148160043514.

rs1481600435 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:52222888 (GRCh38)
3:52256904 (GRCh37)
Canonical SPDI:: NC_000003.12:52222887:G:A
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000003.12:g.52222888G>A, NC_000003.11:g.52256904G>A, NG_033933.1:g.8276C>T, NM_017442.4:c.1428C>T, NM_017442.3:c.1428C>T, NM_138688.1:c.1257C>T

Select item 148147382615.

rs1481473826 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 3:52222686 (GRCh38)
3:52256702 (GRCh37)
Canonical SPDI:: NC_000003.12:52222685:G:
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: -=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000003.12:g.52222686del, NC_000003.11:g.52256702del, NG_033933.1:g.8478del, NM_017442.4:c.1630del, NM_017442.3:c.1630del, NM_138688.1:c.1459del, NP_059138.1:p.Leu544fs

Select item 147920252516.

rs1479202525 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52223790 (GRCh38)
3:52257806 (GRCh37)
Canonical SPDI:: NC_000003.12:52223789:C:T
Gene:: TLR9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000003.12:g.52223790C>T, NC_000003.11:g.52257806C>T, NG_033933.1:g.7374G>A, NM_017442.4:c.526G>A, NM_017442.3:c.526G>A, NM_138688.1:c.355G>A, NP_059138.1:p.Gly176Ser

Select item 147908530217.

rs1479085302 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52222170 (GRCh38)
3:52256186 (GRCh37)
Canonical SPDI:: NC_000003.12:52222169:C:T
Gene:: TLR9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000047/1 (ALFA)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000003.12:g.52222170C>T, NC_000003.11:g.52256186C>T, NG_033933.1:g.8994G>A, NM_017442.4:c.2146G>A, NM_017442.3:c.2146G>A, NM_138688.1:c.1975G>A, NP_059138.1:p.Val716Met

Select item 147778197618.

rs1477781976 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:52223358 (GRCh38)
3:52257374 (GRCh37)
Canonical SPDI:: NC_000003.12:52223357:G:A
Gene:: TLR9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000142/2 (ALFA)
A=0.000019/5 (TOPMED)
HGVS:: NC_000003.12:g.52223358G>A, NC_000003.11:g.52257374G>A, NG_033933.1:g.7806C>T, NM_017442.4:c.958C>T, NM_017442.3:c.958C>T, NM_138688.1:c.787C>T, NP_059138.1:p.Leu320Phe

Select item 147637501819.

rs1476375018 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52221310 (GRCh38)
3:52255326 (GRCh37)
Canonical SPDI:: NC_000003.12:52221309:C:T
Gene:: TLR9 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.52221310C>T, NC_000003.11:g.52255326C>T, NG_033933.1:g.9854G>A, NM_017442.4:c.3006G>A, NM_017442.3:c.3006G>A, NM_138688.1:c.2835G>A

Select item 147622371920.

rs1476223719 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:52223415 (GRCh38)
3:52257431 (GRCh37)
Canonical SPDI:: NC_000003.12:52223414:C:T
Gene:: TLR9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
T=0.000036/5 (GnomAD)
HGVS:: NC_000003.12:g.52223415C>T, NC_000003.11:g.52257431C>T, NG_033933.1:g.7749G>A, NM_017442.4:c.901G>A, NM_017442.3:c.901G>A, NM_138688.1:c.730G>A, NP_059138.1:p.Ala301Thr

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