SNP Links for Protein (Select 961658079) - SNP

Links from Protein

Items: 1 to 20 of 993

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Select item 14904378991.

rs1490437899 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:25479948 (GRCh38)
8:25337464 (GRCh37)
Canonical SPDI:: NC_000008.11:25479947:T:C
Gene:: CDCA2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.25479948T>C, NC_000008.10:g.25337464T>C, NM_152562.4:c.856T>C, NM_152562.3:c.856T>C, NM_152562.2:c.856T>C, NM_001317906.1:c.811T>C, NM_001317907.1:c.856T>C, NP_689775.2:p.Ser286Pro, NP_001304835.1:p.Ser271Pro, NP_001304836.1:p.Ser286Pro

Select item 14888010942.

rs1488801094 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 8:25507302 (GRCh38)
8:25364818 (GRCh37)
Canonical SPDI:: NC_000008.11:25507301:A:T
Gene:: CDCA2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,3_prime_UTR_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.25507302A>T, NC_000008.10:g.25364818A>T, NM_152562.4:c.2636A>T, NM_152562.3:c.2636A>T, NM_152562.2:c.2636A>T, NM_001317906.1:c.2591A>T, NM_001317907.1:c.*747A>T, NP_689775.2:p.Gln879Leu, NP_001304835.1:p.Gln864Leu

Select item 14871901033.

rs1487190103 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:25462068 (GRCh38)
8:25319584 (GRCh37)
Canonical SPDI:: NC_000008.11:25462067:T:C
Gene:: CDCA2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.25462068T>C, NC_000008.10:g.25319584T>C, NM_152562.4:c.247T>C, NM_152562.3:c.247T>C, NM_152562.2:c.247T>C, NM_001317906.1:c.202T>C, NM_001317907.1:c.247T>C, NP_689775.2:p.Tyr83His, NP_001304835.1:p.Tyr68His, NP_001304836.1:p.Tyr83His

Select item 14869822964.

rs1486982296 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:25480061 (GRCh38)
8:25337577 (GRCh37)
Canonical SPDI:: NC_000008.11:25480060:G:A
Gene:: CDCA2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000085/3 (ALFA)
A=0.000036/5 (GnomAD)
A=0.000121/32 (TOPMED)
HGVS:: NC_000008.11:g.25480061G>A, NC_000008.10:g.25337577G>A, NM_152562.4:c.969G>A, NM_152562.3:c.969G>A, NM_152562.2:c.969G>A, NM_001317906.1:c.924G>A, NM_001317907.1:c.969G>A

Select item 14867648755.

rs1486764875 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:25506929 (GRCh38)
8:25364445 (GRCh37)
Canonical SPDI:: NC_000008.11:25506928:A:G
Gene:: CDCA2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.25506929A>G, NC_000008.10:g.25364445A>G, NM_152562.4:c.2263A>G, NM_152562.3:c.2263A>G, NM_152562.2:c.2263A>G, NM_001317906.1:c.2218A>G, NM_001317907.1:c.*374A>G, NP_689775.2:p.Ile755Val, NP_001304835.1:p.Ile740Val

Select item 14866424126.

rs1486642412 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:25503441 (GRCh38)
8:25360957 (GRCh37)
Canonical SPDI:: NC_000008.11:25503440:A:G
Gene:: CDCA2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.25503441A>G, NC_000008.10:g.25360957A>G, NM_152562.4:c.1740A>G, NM_152562.3:c.1740A>G, NM_152562.2:c.1740A>G, NM_001317906.1:c.1695A>G, NM_001317907.1:c.1740A>G

Select item 14865219257.

rs1486521925 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:25468328 (GRCh38)
8:25325844 (GRCh37)
Canonical SPDI:: NC_000008.11:25468327:C:T
Gene:: CDCA2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.25468328C>T, NC_000008.10:g.25325844C>T, NM_152562.4:c.650C>T, NM_152562.3:c.650C>T, NM_152562.2:c.650C>T, NM_001317906.1:c.605C>T, NM_001317907.1:c.650C>T, NP_689775.2:p.Ala217Val, NP_001304835.1:p.Ala202Val, NP_001304836.1:p.Ala217Val

Select item 14864846088.

rs1486484608 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:25506846 (GRCh38)
8:25364362 (GRCh37)
Canonical SPDI:: NC_000008.11:25506845:C:T
Gene:: CDCA2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,3_prime_UTR_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_000008.11:g.25506846C>T, NC_000008.10:g.25364362C>T, NM_152562.4:c.2180C>T, NM_152562.3:c.2180C>T, NM_152562.2:c.2180C>T, NM_001317906.1:c.2135C>T, NM_001317907.1:c.*291C>T, NP_689775.2:p.Pro727Leu, NP_001304835.1:p.Pro712Leu

Select item 14855689239.

rs1485568923 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 8:25484181 (GRCh38)
8:25341697 (GRCh37)
Canonical SPDI:: NC_000008.11:25484180:C:A,NC_000008.11:25484180:C:T
Gene:: CDCA2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.25484181C>A, NC_000008.11:g.25484181C>T, NC_000008.10:g.25341697C>A, NC_000008.10:g.25341697C>T, NM_152562.4:c.1336C>A, NM_152562.4:c.1336C>T, NM_152562.3:c.1336C>A, NM_152562.3:c.1336C>T, NM_152562.2:c.1336C>A, NM_152562.2:c.1336C>T, NM_001317906.1:c.1291C>A, NM_001317906.1:c.1291C>T, NM_001317907.1:c.1336C>A, NM_001317907.1:c.1336C>T, NP_689775.2:p.Pro446Thr, NP_689775.2:p.Pro446Ser, NP_001304835.1:p.Pro431Thr, NP_001304835.1:p.Pro431Ser, NP_001304836.1:p.Pro446Thr, NP_001304836.1:p.Pro446Ser

Select item 148488291210.

rs1484882912 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:25485783 (GRCh38)
8:25343299 (GRCh37)
Canonical SPDI:: NC_000008.11:25485782:T:C
Gene:: CDCA2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.25485783T>C, NC_000008.10:g.25343299T>C, NM_152562.4:c.1390T>C, NM_152562.3:c.1390T>C, NM_152562.2:c.1390T>C, NM_001317906.1:c.1345T>C, NM_001317907.1:c.1390T>C, NP_689775.2:p.Ser464Pro, NP_001304835.1:p.Ser449Pro, NP_001304836.1:p.Ser464Pro

Select item 148417563811.

rs1484175638 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:25488600 (GRCh38)
8:25346116 (GRCh37)
Canonical SPDI:: NC_000008.11:25488599:G:A
Gene:: CDCA2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.25488600G>A, NC_000008.10:g.25346116G>A, NM_152562.4:c.1582G>A, NM_152562.3:c.1582G>A, NM_152562.2:c.1582G>A, NM_001317906.1:c.1537G>A, NM_001317907.1:c.1582G>A, NP_689775.2:p.Glu528Lys, NP_001304835.1:p.Glu513Lys, NP_001304836.1:p.Glu528Lys

Select item 148349392912.

rs1483493929 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:25507687 (GRCh38)
8:25365203 (GRCh37)
Canonical SPDI:: NC_000008.11:25507686:C:T
Gene:: CDCA2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.25507687C>T, NC_000008.10:g.25365203C>T, NG_078515.1:g.295C>T, NM_152562.4:c.3021C>T, NM_152562.3:c.3021C>T, NM_152562.2:c.3021C>T, NM_001317906.1:c.2976C>T, NM_001317907.1:c.*1132C>T

Select item 148254087713.

rs1482540877 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 8:25503487 (GRCh38)
8:25361003 (GRCh37)
Canonical SPDI:: NC_000008.11:25503486:C:G
Gene:: CDCA2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.25503487C>G, NC_000008.10:g.25361003C>G, NM_152562.4:c.1786C>G, NM_152562.3:c.1786C>G, NM_152562.2:c.1786C>G, NM_001317906.1:c.1741C>G, NM_001317907.1:c.1786C>G, NP_689775.2:p.Leu596Val, NP_001304835.1:p.Leu581Val, NP_001304836.1:p.Leu596Val

Select item 148243433014.

rs1482434330 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:25506814 (GRCh38)
8:25364330 (GRCh37)
Canonical SPDI:: NC_000008.11:25506813:T:G
Gene:: CDCA2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.25506814T>G, NC_000008.10:g.25364330T>G, NM_152562.4:c.2148T>G, NM_152562.3:c.2148T>G, NM_152562.2:c.2148T>G, NM_001317906.1:c.2103T>G, NM_001317907.1:c.*259T>G

Select item 148216184115.

rs1482161841 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:25507602 (GRCh38)
8:25365118 (GRCh37)
Canonical SPDI:: NC_000008.11:25507601:G:A
Gene:: CDCA2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000043/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000011/3 (TOPMED)
HGVS:: NC_000008.11:g.25507602G>A, NC_000008.10:g.25365118G>A, NG_078515.1:g.210G>A, NM_152562.4:c.2936G>A, NM_152562.3:c.2936G>A, NM_152562.2:c.2936G>A, NM_001317906.1:c.2891G>A, NM_001317907.1:c.*1047G>A, NP_689775.2:p.Cys979Tyr, NP_001304835.1:p.Cys964Tyr

Select item 148164363116.

rs1481643631 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:25506726 (GRCh38)
8:25364242 (GRCh37)
Canonical SPDI:: NC_000008.11:25506725:A:G
Gene:: CDCA2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.25506726A>G, NC_000008.10:g.25364242A>G, NM_152562.4:c.2060A>G, NM_152562.3:c.2060A>G, NM_152562.2:c.2060A>G, NM_001317906.1:c.2015A>G, NM_001317907.1:c.*171A>G, NP_689775.2:p.Glu687Gly, NP_001304835.1:p.Glu672Gly

Select item 148147766617.

rs1481477666 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 8:25507656 (GRCh38)
8:25365173 (GRCh37)
Canonical SPDI:: NC_000008.11:25507656:AA:AAA
Gene:: CDCA2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: AAA=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.25507658dup, NC_000008.10:g.25365174dup, NG_078515.1:g.266dup, NM_152562.4:c.2992dup, NM_152562.3:c.2992dup, NM_152562.2:c.2992dup, NM_001317906.1:c.2947dup, NM_001317907.1:c.*1103dup, NP_689775.2:p.Arg998fs, NP_001304835.1:p.Arg983fs

Select item 148082748718.

rs1480827487 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:25507438 (GRCh38)
8:25364954 (GRCh37)
Canonical SPDI:: NC_000008.11:25507437:A:G
Gene:: CDCA2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.25507438A>G, NC_000008.10:g.25364954A>G, NG_078515.1:g.46A>G, NM_152562.4:c.2772A>G, NM_152562.3:c.2772A>G, NM_152562.2:c.2772A>G, NM_001317906.1:c.2727A>G, NM_001317907.1:c.*883A>G, NP_689775.2:p.Ile924Met, NP_001304835.1:p.Ile909Met

Select item 148070287719.

rs1480702877 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:25469927 (GRCh38)
8:25327443 (GRCh37)
Canonical SPDI:: NC_000008.11:25469926:G:A
Gene:: CDCA2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.25469927G>A, NC_000008.10:g.25327443G>A, NM_152562.4:c.767G>A, NM_152562.3:c.767G>A, NM_152562.2:c.767G>A, NM_001317906.1:c.722G>A, NM_001317907.1:c.767G>A, NP_689775.2:p.Gly256Glu, NP_001304835.1:p.Gly241Glu, NP_001304836.1:p.Gly256Glu

Select item 148012344220.

rs1480123442 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:25507354 (GRCh38)
8:25364870 (GRCh37)
Canonical SPDI:: NC_000008.11:25507353:A:G
Gene:: CDCA2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000008.11:g.25507354A>G, NC_000008.10:g.25364870A>G, NM_152562.4:c.2688A>G, NM_152562.3:c.2688A>G, NM_152562.2:c.2688A>G, NM_001317906.1:c.2643A>G, NM_001317907.1:c.*799A>G

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