SNP Links for Protein (Select 1041214568) - SNP

Links from Protein

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Select item 14752411351.

rs1475241135 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:159713591 (GRCh38)
1:159683381 (GRCh37)
Canonical SPDI:: NC_000001.11:159713590:C:G
Gene:: CRP (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.000047/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.159713591C>G, NC_000001.10:g.159683381C>G, NG_013007.1:g.5999G>C, NM_000567.3:c.609G>C, NM_000567.2:c.609G>C, NM_001329057.2:c.609G>C, NM_001329057.1:c.609G>C, NM_001329058.2:c.210G>C, NM_001329058.1:c.210G>C, NM_001382703.1:c.243G>C

Select item 14698960712.

rs1469896071 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:159714442 (GRCh38)
1:159684232 (GRCh37)
Canonical SPDI:: NC_000001.11:159714441:T:C
Gene:: CRP (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.159714442T>C, NC_000001.10:g.159684232T>C, NG_013007.1:g.5148A>G, NM_000567.3:c.44A>G, NM_000567.2:c.44A>G, NM_001329057.2:c.44A>G, NM_001329057.1:c.44A>G, NM_001329058.2:c.44A>G, NM_001329058.1:c.44A>G, NM_001382703.1:c.44A>G, NP_000558.2:p.His15Arg, NP_001315986.1:p.His15Arg, NP_001315987.1:p.His15Arg, NP_001369632.1:p.His15Arg

Select item 14557332963.

rs1455733296 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:159714009 (GRCh38)
1:159683799 (GRCh37)
Canonical SPDI:: NC_000001.11:159714008:G:A
Gene:: CRP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.159714009G>A, NC_000001.10:g.159683799G>A, NG_013007.1:g.5581C>T, NM_000567.3:c.191C>T, NM_000567.2:c.191C>T, NM_001329057.2:c.191C>T, NM_001329057.1:c.191C>T, NM_001329058.2:c.191C>T, NM_001329058.1:c.191C>T, NM_001382703.1:c.191C>T, NP_000558.2:p.Thr64Ile, NP_001315986.1:p.Thr64Ile, NP_001315987.1:p.Thr64Ile, NP_001369632.1:p.Thr64Ile

Select item 14528621464.

rs1452862146 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:159714088 (GRCh38)
1:159683878 (GRCh37)
Canonical SPDI:: NC_000001.11:159714087:C:G,NC_000001.11:159714087:C:T
Gene:: CRP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.159714088C>G, NC_000001.11:g.159714088C>T, NC_000001.10:g.159683878C>G, NC_000001.10:g.159683878C>T, NG_013007.1:g.5502G>C, NG_013007.1:g.5502G>A, NM_000567.3:c.112G>C, NM_000567.3:c.112G>A, NM_000567.2:c.112G>C, NM_000567.2:c.112G>A, NM_001329057.2:c.112G>C, NM_001329057.2:c.112G>A, NM_001329057.1:c.112G>C, NM_001329057.1:c.112G>A, NM_001329058.2:c.112G>C, NM_001329058.2:c.112G>A, NM_001329058.1:c.112G>C, NM_001329058.1:c.112G>A, NM_001382703.1:c.112G>C, NM_001382703.1:c.112G>A, NP_000558.2:p.Val38Leu, NP_000558.2:p.Val38Ile, NP_001315986.1:p.Val38Leu, NP_001315986.1:p.Val38Ile, NP_001315987.1:p.Val38Leu, NP_001315987.1:p.Val38Ile, NP_001369632.1:p.Val38Leu, NP_001369632.1:p.Val38Ile

Select item 14464917695.

rs1446491769 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:159713552 (GRCh38)
1:159683342 (GRCh37)
Canonical SPDI:: NC_000001.11:159713551:C:A
Gene:: CRP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.159713552C>A, NC_000001.10:g.159683342C>A, NG_013007.1:g.6038G>T, NM_000567.3:c.648G>T, NM_000567.2:c.648G>T, NM_001329057.2:c.648G>T, NM_001329057.1:c.648G>T, NM_001329058.2:c.249G>T, NM_001329058.1:c.249G>T, NM_001382703.1:c.282G>T

Select item 14394773016.

rs1439477301 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:159714021 (GRCh38)
1:159683811 (GRCh37)
Canonical SPDI:: NC_000001.11:159714020:T:A
Gene:: CRP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.159714021T>A, NC_000001.10:g.159683811T>A, NG_013007.1:g.5569A>T, NM_000567.3:c.179A>T, NM_000567.2:c.179A>T, NM_001329057.2:c.179A>T, NM_001329057.1:c.179A>T, NM_001329058.2:c.179A>T, NM_001329058.1:c.179A>T, NM_001382703.1:c.179A>T, NP_000558.2:p.Glu60Val, NP_001315986.1:p.Glu60Val, NP_001315987.1:p.Glu60Val, NP_001369632.1:p.Glu60Val

Select item 14124124127.

rs1412412412 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:159713531 (GRCh38)
1:159683321 (GRCh37)
Canonical SPDI:: NC_000001.11:159713530:C:T
Gene:: CRP (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000057/2 (ALFA)
T=0.000019/5 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000001.11:g.159713531C>T, NC_000001.10:g.159683321C>T, NG_013007.1:g.6059G>A, NM_000567.3:c.669G>A, NM_000567.2:c.669G>A, NM_001329057.2:c.669G>A, NM_001329057.1:c.669G>A, NM_001329058.2:c.270G>A, NM_001329058.1:c.270G>A, NM_001382703.1:c.303G>A, NP_000558.2:p.Trp223Ter, NP_001315986.1:p.Trp223Ter, NP_001315987.1:p.Trp90Ter, NP_001369632.1:p.Trp101Ter

Select item 14111976868.

rs1411197686 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:159714132 (GRCh38)
1:159683922 (GRCh37)
Canonical SPDI:: NC_000001.11:159714131:G:A,NC_000001.11:159714131:G:C
Gene:: CRP (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.159714132G>A, NC_000001.11:g.159714132G>C, NC_000001.10:g.159683922G>A, NC_000001.10:g.159683922G>C, NG_013007.1:g.5458C>T, NG_013007.1:g.5458C>G, NM_000567.3:c.68C>T, NM_000567.3:c.68C>G, NM_000567.2:c.68C>T, NM_000567.2:c.68C>G, NM_001329057.2:c.68C>T, NM_001329057.2:c.68C>G, NM_001329057.1:c.68C>T, NM_001329057.1:c.68C>G, NM_001329058.2:c.68C>T, NM_001329058.2:c.68C>G, NM_001329058.1:c.68C>T, NM_001329058.1:c.68C>G, NM_001382703.1:c.68C>T, NM_001382703.1:c.68C>G, NP_000558.2:p.Ser23Leu, NP_000558.2:p.Ser23Trp, NP_001315986.1:p.Ser23Leu, NP_001315986.1:p.Ser23Trp, NP_001315987.1:p.Ser23Leu, NP_001315987.1:p.Ser23Trp, NP_001369632.1:p.Ser23Leu, NP_001369632.1:p.Ser23Trp

Select item 13930134599.

rs1393013459 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:159714058 (GRCh38)
1:159683848 (GRCh37)
Canonical SPDI:: NC_000001.11:159714057:G:A
Gene:: CRP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.159714058G>A, NC_000001.10:g.159683848G>A, NG_013007.1:g.5532C>T, NM_000567.3:c.142C>T, NM_000567.2:c.142C>T, NM_001329057.2:c.142C>T, NM_001329057.1:c.142C>T, NM_001329058.2:c.142C>T, NM_001329058.1:c.142C>T, NM_001382703.1:c.142C>T, NP_000558.2:p.Leu48Phe, NP_001315986.1:p.Leu48Phe, NP_001315987.1:p.Leu48Phe, NP_001369632.1:p.Leu48Phe

Select item 138607133410.

rs1386071334 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:159713542 (GRCh38)
1:159683332 (GRCh37)
Canonical SPDI:: NC_000001.11:159713541:G:A,NC_000001.11:159713541:G:C
Gene:: CRP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.159713542G>A, NC_000001.11:g.159713542G>C, NC_000001.10:g.159683332G>A, NC_000001.10:g.159683332G>C, NG_013007.1:g.6048C>T, NG_013007.1:g.6048C>G, NM_000567.3:c.658C>T, NM_000567.3:c.658C>G, NM_000567.2:c.658C>T, NM_000567.2:c.658C>G, NM_001329057.2:c.658C>T, NM_001329057.2:c.658C>G, NM_001329057.1:c.658C>T, NM_001329057.1:c.658C>G, NM_001329058.2:c.259C>T, NM_001329058.2:c.259C>G, NM_001329058.1:c.259C>T, NM_001329058.1:c.259C>G, NM_001382703.1:c.292C>T, NM_001382703.1:c.292C>G, NP_000558.2:p.Pro220Ser, NP_000558.2:p.Pro220Ala, NP_001315986.1:p.Pro220Ser, NP_001315986.1:p.Pro220Ala, NP_001315987.1:p.Pro87Ser, NP_001315987.1:p.Pro87Ala, NP_001369632.1:p.Pro98Ser, NP_001369632.1:p.Pro98Ala

Select item 137671148511.

rs1376711485 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 1:159714018 (GRCh38)
1:159683808 (GRCh37)
Canonical SPDI:: NC_000001.11:159714017:A:G,NC_000001.11:159714017:A:T
Gene:: CRP (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000028/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.159714018A>G, NC_000001.11:g.159714018A>T, NC_000001.10:g.159683808A>G, NC_000001.10:g.159683808A>T, NG_013007.1:g.5572T>C, NG_013007.1:g.5572T>A, NM_000567.3:c.182T>C, NM_000567.3:c.182T>A, NM_000567.2:c.182T>C, NM_000567.2:c.182T>A, NM_001329057.2:c.182T>C, NM_001329057.2:c.182T>A, NM_001329057.1:c.182T>C, NM_001329057.1:c.182T>A, NM_001329058.2:c.182T>C, NM_001329058.2:c.182T>A, NM_001329058.1:c.182T>C, NM_001329058.1:c.182T>A, NM_001382703.1:c.182T>C, NM_001382703.1:c.182T>A, NP_000558.2:p.Leu61Pro, NP_000558.2:p.Leu61Gln, NP_001315986.1:p.Leu61Pro, NP_001315986.1:p.Leu61Gln, NP_001315987.1:p.Leu61Pro, NP_001315987.1:p.Leu61Gln, NP_001369632.1:p.Leu61Pro, NP_001369632.1:p.Leu61Gln

Select item 134773562212.

rs1347735622 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:159714028 (GRCh38)
1:159683818 (GRCh37)
Canonical SPDI:: NC_000001.11:159714027:A:T
Gene:: CRP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.159714028A>T, NC_000001.10:g.159683818A>T, NG_013007.1:g.5562T>A, NM_000567.3:c.172T>A, NM_000567.2:c.172T>A, NM_001329057.2:c.172T>A, NM_001329057.1:c.172T>A, NM_001329058.2:c.172T>A, NM_001329058.1:c.172T>A, NM_001382703.1:c.172T>A, NP_000558.2:p.Tyr58Asn, NP_001315986.1:p.Tyr58Asn, NP_001315987.1:p.Tyr58Asn, NP_001369632.1:p.Tyr58Asn

Select item 133802092213.

rs1338020922 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:159714089 (GRCh38)
1:159683879 (GRCh37)
Canonical SPDI:: NC_000001.11:159714088:A:G
Gene:: CRP (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.159714089A>G, NC_000001.10:g.159683879A>G, NG_013007.1:g.5501T>C, NM_000567.3:c.111T>C, NM_000567.2:c.111T>C, NM_001329057.2:c.111T>C, NM_001329057.1:c.111T>C, NM_001329058.2:c.111T>C, NM_001329058.1:c.111T>C, NM_001382703.1:c.111T>C

Select item 132354315714.

rs1323543157 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GGGA [Show Flanks]
Chromosome:: 1:159714079 (GRCh38)
1:159683870 (GRCh37)
Canonical SPDI:: NC_000001.11:159714079:GAGGGA:GAGGGAGGGA
Gene:: CRP (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: GAGG=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.159714082_159714085dup, NC_000001.10:g.159683872_159683875dup, NG_013007.1:g.5507_5510dup, NM_000567.3:c.117_120dup, NM_000567.2:c.117_120dup, NM_001329057.2:c.117_120dup, NM_001329057.1:c.117_120dup, NM_001329058.2:c.117_120dup, NM_001329058.1:c.117_120dup, NM_001382703.1:c.117_120dup, NP_000558.2:p.Lys41fs, NP_001315986.1:p.Lys41fs, NP_001315987.1:p.Lys41fs, NP_001369632.1:p.Lys41fs

Select item 131939737615.

rs1319397376 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 1:159713546 (GRCh38)
1:159683336 (GRCh37)
Canonical SPDI:: NC_000001.11:159713545:GG:G
Gene:: CRP (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.159713547del, NC_000001.10:g.159683337del, NG_013007.1:g.6044del, NM_000567.3:c.654del, NM_000567.2:c.654del, NM_001329057.2:c.654del, NM_001329057.1:c.654del, NM_001329058.2:c.255del, NM_001329058.1:c.255del, NM_001382703.1:c.288del, NP_000558.2:p.Lys219fs, NP_001315986.1:p.Lys219fs, NP_001315987.1:p.Lys86fs, NP_001369632.1:p.Lys97fs

Select item 130938801216.

rs1309388012 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:159714101 (GRCh38)
1:159683891 (GRCh37)
Canonical SPDI:: NC_000001.11:159714100:C:T
Gene:: CRP (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000012/3 (GnomAD_exomes)
T=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.159714101C>T, NC_000001.10:g.159683891C>T, NG_013007.1:g.5489G>A, NM_000567.3:c.99G>A, NM_000567.2:c.99G>A, NM_001329057.2:c.99G>A, NM_001329057.1:c.99G>A, NM_001329058.2:c.99G>A, NM_001329058.1:c.99G>A, NM_001382703.1:c.99G>A

Select item 130373018717.

rs1303730187 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 1:159714059 (GRCh38)
1:159683849 (GRCh37)
Canonical SPDI:: NC_000001.11:159714058:A:G,NC_000001.11:159714058:A:T
Gene:: CRP (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.159714059A>G, NC_000001.11:g.159714059A>T, NC_000001.10:g.159683849A>G, NC_000001.10:g.159683849A>T, NG_013007.1:g.5531T>C, NG_013007.1:g.5531T>A, NM_000567.3:c.141T>C, NM_000567.3:c.141T>A, NM_000567.2:c.141T>C, NM_000567.2:c.141T>A, NM_001329057.2:c.141T>C, NM_001329057.2:c.141T>A, NM_001329057.1:c.141T>C, NM_001329057.1:c.141T>A, NM_001329058.2:c.141T>C, NM_001329058.2:c.141T>A, NM_001329058.1:c.141T>C, NM_001329058.1:c.141T>A, NM_001382703.1:c.141T>C, NM_001382703.1:c.141T>A

Select item 127553404518.

rs1275534045 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:159714119 (GRCh38)
1:159683909 (GRCh37)
Canonical SPDI:: NC_000001.11:159714118:A:C
Gene:: CRP (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000001.11:g.159714119A>C, NC_000001.10:g.159683909A>C, NG_013007.1:g.5471T>G, NM_000567.3:c.81T>G, NM_000567.2:c.81T>G, NM_001329057.2:c.81T>G, NM_001329057.1:c.81T>G, NM_001329058.2:c.81T>G, NM_001329058.1:c.81T>G, NM_001382703.1:c.81T>G, NP_000558.2:p.Phe27Leu, NP_001315986.1:p.Phe27Leu, NP_001315987.1:p.Phe27Leu, NP_001369632.1:p.Phe27Leu

Select item 126896843519.

rs1268968435 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:159714133 (GRCh38)
1:159683923 (GRCh37)
Canonical SPDI:: NC_000001.11:159714132:A:C
Gene:: CRP (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.159714133A>C, NC_000001.10:g.159683923A>C, NG_013007.1:g.5457T>G, NM_000567.3:c.67T>G, NM_000567.2:c.67T>G, NM_001329057.2:c.67T>G, NM_001329057.1:c.67T>G, NM_001329058.2:c.67T>G, NM_001329058.1:c.67T>G, NM_001382703.1:c.67T>G, NP_000558.2:p.Ser23Ala, NP_001315986.1:p.Ser23Ala, NP_001315987.1:p.Ser23Ala, NP_001369632.1:p.Ser23Ala

Select item 126646201120.

rs1266462011 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:159713566 (GRCh38)
1:159683356 (GRCh37)
Canonical SPDI:: NC_000001.11:159713565:C:G
Gene:: CRP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.159713566C>G, NC_000001.10:g.159683356C>G, NG_013007.1:g.6024G>C, NM_000567.3:c.634G>C, NM_000567.2:c.634G>C, NM_001329057.2:c.634G>C, NM_001329057.1:c.634G>C, NM_001329058.2:c.235G>C, NM_001329058.1:c.235G>C, NM_001382703.1:c.268G>C, NP_000558.2:p.Val212Leu, NP_001315986.1:p.Val212Leu, NP_001315987.1:p.Val79Leu, NP_001369632.1:p.Val90Leu

dbSNP

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