SNP Links for Protein (Select 808175990) - SNP

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Links from Protein

Items: 1 to 20 of 869

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Select item 14905583371.

rs1490558337 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:64802066 (GRCh38)
11:64569538 (GRCh37)
Canonical SPDI:: NC_000011.10:64802065:C:T
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000011.10:g.64802066C>T, NC_000011.9:g.64569538C>T, NG_033040.1:g.6176G>A, NM_004579.5:c.366G>A, NM_004579.4:c.366G>A, NM_004579.3:c.366G>A, NM_001307990.2:c.366G>A, NM_001307990.1:c.366G>A, NG_008929.1:g.14229G>A

Select item 14901306832.

rs1490130683 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:64796496 (GRCh38)
11:64563968 (GRCh37)
Canonical SPDI:: NC_000011.10:64796495:A:G
Gene:: MAP4K2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000011.10:g.64796496A>G, NC_000011.9:g.64563968A>G, NG_033040.1:g.11746T>C, NM_004579.5:c.1630T>C, NM_004579.4:c.1630T>C, NM_004579.3:c.1630T>C, NM_001307990.2:c.1606T>C, NM_001307990.1:c.1606T>C, NG_079319.1:g.440A>G, NP_004570.2:p.Ser544Pro, NP_001294919.1:p.Ser536Pro

Select item 14874220613.

rs1487422061 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:64800322 (GRCh38)
11:64567794 (GRCh37)
Canonical SPDI:: NC_000011.10:64800321:T:C
Gene:: MAP4K2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.64800322T>C, NC_000011.9:g.64567794T>C, NG_033040.1:g.7920A>G, NM_004579.5:c.796A>G, NM_004579.4:c.796A>G, NM_004579.3:c.796A>G, NM_001307990.2:c.796A>G, NM_001307990.1:c.796A>G, NP_004570.2:p.Lys266Glu, NP_001294919.1:p.Lys266Glu

Select item 14867688594.

rs1486768859 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:64798801 (GRCh38)
11:64566273 (GRCh37)
Canonical SPDI:: NC_000011.10:64798800:A:T
Gene:: MAP4K2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000043/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.64798801A>T, NC_000011.9:g.64566273A>T, NG_033040.1:g.9441T>A, NM_004579.5:c.1090T>A, NM_004579.4:c.1090T>A, NM_004579.3:c.1090T>A, NM_001307990.2:c.1090T>A, NM_001307990.1:c.1090T>A, NP_004570.2:p.Leu364Met, NP_001294919.1:p.Leu364Met

Select item 14865869355.

rs1486586935 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:64791912 (GRCh38)
11:64559384 (GRCh37)
Canonical SPDI:: NC_000011.10:64791911:G:C
Gene:: MAP4K2 (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_000011.10:g.64791912G>C, NC_000011.9:g.64559384G>C, NG_033040.1:g.16330C>G, NM_004579.5:c.2089C>G, NM_004579.4:c.2089C>G, NM_004579.3:c.2089C>G, NM_001307990.2:c.2065C>G, NM_001307990.1:c.2065C>G, NP_004570.2:p.Pro697Ala, NP_001294919.1:p.Pro689Ala

Select item 14837770286.

rs1483777028 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:64796840 (GRCh38)
11:64564312 (GRCh37)
Canonical SPDI:: NC_000011.10:64796839:A:C
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.64796840A>C, NC_000011.9:g.64564312A>C, NG_033040.1:g.11402T>G, NM_004579.5:c.1461T>G, NM_004579.4:c.1461T>G, NM_004579.3:c.1461T>G, NM_001307990.2:c.1437T>G, NM_001307990.1:c.1437T>G

Select item 14829312517.

rs1482931251 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:64789743 (GRCh38)
11:64557215 (GRCh37)
Canonical SPDI:: NC_000011.10:64789742:G:C
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.64789743G>C, NC_000011.9:g.64557215G>C, NG_033040.1:g.18499C>G, NM_004579.5:c.2362C>G, NM_004579.4:c.2362C>G, NM_004579.3:c.2362C>G, NM_001307990.2:c.2338C>G, NM_001307990.1:c.2338C>G, NP_004570.2:p.Leu788Val, NP_001294919.1:p.Leu780Val

Select item 14823504658.

rs1482350465 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:64792025 (GRCh38)
11:64559497 (GRCh37)
Canonical SPDI:: NC_000011.10:64792024:T:C
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0.000111/1 (ALFA)
C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.64792025T>C, NC_000011.9:g.64559497T>C, NG_033040.1:g.16217A>G, NM_004579.5:c.1976A>G, NM_004579.4:c.1976A>G, NM_004579.3:c.1976A>G, NM_001307990.2:c.1952A>G, NM_001307990.1:c.1952A>G, NP_004570.2:p.Lys659Arg, NP_001294919.1:p.Lys651Arg

Select item 14820698169.

rs1482069816 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:64797531 (GRCh38)
11:64565003 (GRCh37)
Canonical SPDI:: NC_000011.10:64797530:A:G
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000011.10:g.64797531A>G, NC_000011.9:g.64565003A>G, NG_033040.1:g.10711T>C, NM_004579.5:c.1140T>C, NM_004579.4:c.1140T>C, NM_004579.3:c.1140T>C, NM_001307990.2:c.1140T>C, NM_001307990.1:c.1140T>C

Select item 147818335110.

rs1478183351 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:64792036 (GRCh38)
11:64559508 (GRCh37)
Canonical SPDI:: NC_000011.10:64792035:C:T
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000011.10:g.64792036C>T, NC_000011.9:g.64559508C>T, NG_033040.1:g.16206G>A, NM_004579.5:c.1965G>A, NM_004579.4:c.1965G>A, NM_004579.3:c.1965G>A, NM_001307990.2:c.1941G>A, NM_001307990.1:c.1941G>A

Select item 147789870411.

rs1477898704 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:64800361 (GRCh38)
11:64567833 (GRCh37)
Canonical SPDI:: NC_000011.10:64800360:C:T
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000047/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.64800361C>T, NC_000011.9:g.64567833C>T, NG_033040.1:g.7881G>A, NM_004579.5:c.757G>A, NM_004579.4:c.757G>A, NM_004579.3:c.757G>A, NM_001307990.2:c.757G>A, NM_001307990.1:c.757G>A, NP_004570.2:p.Ala253Thr, NP_001294919.1:p.Ala253Thr

Select item 147752831612.

rs1477528316 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:64789952 (GRCh38)
11:64557424 (GRCh37)
Canonical SPDI:: NC_000011.10:64789951:C:T
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.64789952C>T, NC_000011.9:g.64557424C>T, NG_033040.1:g.18290G>A, NM_004579.5:c.2256G>A, NM_004579.4:c.2256G>A, NM_004579.3:c.2256G>A, NM_001307990.2:c.2232G>A, NM_001307990.1:c.2232G>A

Select item 147562406813.

rs1475624068 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:64802435 (GRCh38)
11:64569907 (GRCh37)
Canonical SPDI:: NC_000011.10:64802434:C:T
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000011.10:g.64802435C>T, NC_000011.9:g.64569907C>T, NG_033040.1:g.5807G>A, NM_004579.5:c.294G>A, NM_004579.4:c.294G>A, NM_004579.3:c.294G>A, NM_001307990.2:c.294G>A, NM_001307990.1:c.294G>A, NG_008929.1:g.13860G>A

Select item 147472842214.

rs1474728422 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:64800980 (GRCh38)
11:64568452 (GRCh37)
Canonical SPDI:: NC_000011.10:64800979:T:C
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000008/2 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.64800980T>C, NC_000011.9:g.64568452T>C, NG_033040.1:g.7262A>G, NM_004579.5:c.582A>G, NM_004579.4:c.582A>G, NM_004579.3:c.582A>G, NM_001307990.2:c.582A>G, NM_001307990.1:c.582A>G

Select item 147362217315.

rs1473622173 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:64789769 (GRCh38)
11:64557241 (GRCh37)
Canonical SPDI:: NC_000011.10:64789768:G:A
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.64789769G>A, NC_000011.9:g.64557241G>A, NG_033040.1:g.18473C>T, NM_004579.5:c.2336C>T, NM_004579.4:c.2336C>T, NM_004579.3:c.2336C>T, NM_001307990.2:c.2312C>T, NM_001307990.1:c.2312C>T, NP_004570.2:p.Thr779Ile, NP_001294919.1:p.Thr771Ile

Select item 147277033116.

rs1472770331 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:64792231 (GRCh38)
11:64559703 (GRCh37)
Canonical SPDI:: NC_000011.10:64792230:G:A
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000011.10:g.64792231G>A, NC_000011.9:g.64559703G>A, NG_033040.1:g.16011C>T, NM_004579.5:c.1855C>T, NM_004579.4:c.1855C>T, NM_004579.3:c.1855C>T, NM_001307990.2:c.1831C>T, NM_001307990.1:c.1831C>T, NP_004570.2:p.Pro619Ser, NP_001294919.1:p.Pro611Ser

Select item 147081536817.

rs1470815368 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:64798810 (GRCh38)
11:64566282 (GRCh37)
Canonical SPDI:: NC_000011.10:64798809:T:C
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.64798810T>C, NC_000011.9:g.64566282T>C, NG_033040.1:g.9432A>G, NM_004579.5:c.1081A>G, NM_004579.4:c.1081A>G, NM_004579.3:c.1081A>G, NM_001307990.2:c.1081A>G, NM_001307990.1:c.1081A>G, NP_004570.2:p.Lys361Glu, NP_001294919.1:p.Lys361Glu

Select item 147065111618.

rs1470651116 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:64801126 (GRCh38)
11:64568598 (GRCh37)
Canonical SPDI:: NC_000011.10:64801125:A:G
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000011.10:g.64801126A>G, NC_000011.9:g.64568598A>G, NG_033040.1:g.7116T>C, NM_004579.5:c.515T>C, NM_004579.4:c.515T>C, NM_004579.3:c.515T>C, NM_001307990.2:c.515T>C, NM_001307990.1:c.515T>C, NP_004570.2:p.Ile172Thr, NP_001294919.1:p.Ile172Thr

Select item 147052706119.

rs1470527061 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:64801601 (GRCh38)
11:64569073 (GRCh37)
Canonical SPDI:: NC_000011.10:64801600:A:T
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000011.10:g.64801601A>T, NC_000011.9:g.64569073A>T, NG_033040.1:g.6641T>A, NM_004579.5:c.435T>A, NM_004579.4:c.435T>A, NM_004579.3:c.435T>A, NM_001307990.2:c.435T>A, NM_001307990.1:c.435T>A, NG_008929.1:g.14694T>A

Select item 146929150820.

rs1469291508 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:64796677 (GRCh38)
11:64564149 (GRCh37)
Canonical SPDI:: NC_000011.10:64796676:T:C
Gene:: MAP4K2 (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_000011.10:g.64796677T>C, NC_000011.9:g.64564149T>C, NG_033040.1:g.11565A>G, NM_004579.5:c.1529A>G, NM_004579.4:c.1529A>G, NM_004579.3:c.1529A>G, NM_001307990.2:c.1505A>G, NM_001307990.1:c.1505A>G, NP_004570.2:p.Tyr510Cys, NP_001294919.1:p.Tyr502Cys

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