SNP Links for Protein (Select 6912348) - SNP

Links from Protein

Items: 1 to 20 of 355

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Select item 14866182071.

rs1486618207 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 1:84866059 (GRCh38)
1:85331742 (GRCh37)
Canonical SPDI:: NC_000001.11:84866058:G:C,NC_000001.11:84866058:G:T
Gene:: LPAR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (GnomAD)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.84866059G>C, NC_000001.11:g.84866059G>T, NC_000001.10:g.85331742G>C, NC_000001.10:g.85331742G>T, NM_012152.3:c.62C>G, NM_012152.3:c.62C>A, NM_012152.2:c.62C>G, NM_012152.2:c.62C>A, NP_036284.1:p.Thr21Ser, NP_036284.1:p.Thr21Asn

Select item 14814495422.

rs1481449542 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:84865559 (GRCh38)
1:85331242 (GRCh37)
Canonical SPDI:: NC_000001.11:84865558:G:T
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000001.11:g.84865559G>T, NC_000001.10:g.85331242G>T, NM_012152.3:c.562C>A, NM_012152.2:c.562C>A, NP_036284.1:p.Leu188Ile

Select item 14808295903.

rs1480829590 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>- [Show Flanks]
Chromosome:: 1:84866022 (GRCh38)
1:85331705 (GRCh37)
Canonical SPDI:: NC_000001.11:84866019:AAAA:AA
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAA=0.000071/1 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.84866022_84866023del, NC_000001.10:g.85331705_85331706del, NM_012152.3:c.100_101del, NM_012152.2:c.100_101del, NP_036284.1:p.Leu34fs

Select item 14792968294.

rs1479296829 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:84865613 (GRCh38)
1:85331296 (GRCh37)
Canonical SPDI:: NC_000001.11:84865612:G:C
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: C=0.00004/1 (TOMMO)
HGVS:: NC_000001.11:g.84865613G>C, NC_000001.10:g.85331296G>C, NM_012152.3:c.508C>G, NM_012152.2:c.508C>G, NP_036284.1:p.Leu170Val

Select item 14746143045.

rs1474614304 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:84866075 (GRCh38)
1:85331758 (GRCh37)
Canonical SPDI:: NC_000001.11:84866074:T:C
Gene:: LPAR3 (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)
C=0.000023/6 (TOPMED)
HGVS:: NC_000001.11:g.84866075T>C, NC_000001.10:g.85331758T>C, NM_012152.3:c.46A>G, NM_012152.2:c.46A>G, NP_036284.1:p.Arg16Gly

Select item 14735045556.

rs1473504555 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:84865828 (GRCh38)
1:85331511 (GRCh37)
Canonical SPDI:: NC_000001.11:84865827:G:T
Gene:: LPAR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.84865828G>T, NC_000001.10:g.85331511G>T, NM_012152.3:c.293C>A, NM_012152.2:c.293C>A, NP_036284.1:p.Thr98Asn

Select item 14725223627.

rs1472522362 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:84865417 (GRCh38)
1:85331100 (GRCh37)
Canonical SPDI:: NC_000001.11:84865416:A:G
Gene:: LPAR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.84865417A>G, NC_000001.10:g.85331100A>G, NM_012152.3:c.704T>C, NM_012152.2:c.704T>C, NP_036284.1:p.Met235Thr

Select item 14615204838.

rs1461520483 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:84865422 (GRCh38)
1:85331105 (GRCh37)
Canonical SPDI:: NC_000001.11:84865421:T:C
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.84865422T>C, NC_000001.10:g.85331105T>C, NM_012152.3:c.699A>G, NM_012152.2:c.699A>G

Select item 14614562039.

rs1461456203 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:84813934 (GRCh38)
1:85279617 (GRCh37)
Canonical SPDI:: NC_000001.11:84813933:G:A,NC_000001.11:84813933:G:T
Gene:: LPAR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.84813934G>A, NC_000001.11:g.84813934G>T, NC_000001.10:g.85279617G>A, NC_000001.10:g.85279617G>T, NM_012152.3:c.974C>T, NM_012152.3:c.974C>A, NM_012152.2:c.974C>T, NM_012152.2:c.974C>A, NP_036284.1:p.Ser325Phe, NP_036284.1:p.Ser325Tyr

Select item 146113634310.

rs1461136343 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:84865465 (GRCh38)
1:85331148 (GRCh37)
Canonical SPDI:: NC_000001.11:84865464:A:G
Gene:: LPAR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.84865465A>G, NC_000001.10:g.85331148A>G, NM_012152.3:c.656T>C, NM_012152.2:c.656T>C, NP_036284.1:p.Val219Ala

Select item 145983704511.

rs1459837045 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:84813903 (GRCh38)
1:85279586 (GRCh37)
Canonical SPDI:: NC_000001.11:84813902:G:T
Gene:: LPAR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.84813903G>T, NC_000001.10:g.85279586G>T, NM_012152.3:c.1005C>A, NM_012152.2:c.1005C>A, NP_036284.1:p.Ser335Arg

Select item 145875892812.

rs1458758928 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:84865934 (GRCh38)
1:85331617 (GRCh37)
Canonical SPDI:: NC_000001.11:84865933:A:G
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.84865934A>G, NC_000001.10:g.85331617A>G, NM_012152.3:c.187T>C, NM_012152.2:c.187T>C, NP_036284.1:p.Phe63Leu

Select item 145382217713.

rs1453822177 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:84865728 (GRCh38)
1:85331411 (GRCh37)
Canonical SPDI:: NC_000001.11:84865727:G:C
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.84865728G>C, NC_000001.10:g.85331411G>C, NM_012152.3:c.393C>G, NM_012152.2:c.393C>G, NP_036284.1:p.Ile131Met

Select item 144995752614.

rs1449957526 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:84814029 (GRCh38)
1:85279712 (GRCh37)
Canonical SPDI:: NC_000001.11:84814028:G:A
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.84814029G>A, NC_000001.10:g.85279712G>A, NM_012152.3:c.879C>T, NM_012152.2:c.879C>T

Select item 144936807115.

rs1449368071 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:84866052 (GRCh38)
1:85331735 (GRCh37)
Canonical SPDI:: NC_000001.11:84866051:A:G
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.84866052A>G, NC_000001.10:g.85331735A>G, NM_012152.3:c.69T>C, NM_012152.2:c.69T>C

Select item 144821440016.

rs1448214400 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:84865408 (GRCh38)
1:85331091 (GRCh37)
Canonical SPDI:: NC_000001.11:84865407:A:G
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.84865408A>G, NC_000001.10:g.85331091A>G, NM_012152.3:c.713T>C, NM_012152.2:c.713T>C, NP_036284.1:p.Met238Thr

Select item 144660154717.

rs1446601547 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:84865710 (GRCh38)
1:85331393 (GRCh37)
Canonical SPDI:: NC_000001.11:84865709:A:G
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.84865710A>G, NC_000001.10:g.85331393A>G, NM_012152.3:c.411T>C, NM_012152.2:c.411T>C

Select item 144562393718.

rs1445623937 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:84866083 (GRCh38)
1:85331766 (GRCh37)
Canonical SPDI:: NC_000001.11:84866082:A:G
Gene:: LPAR3 (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_000001.11:g.84866083A>G, NC_000001.10:g.85331766A>G, NM_012152.3:c.38T>C, NM_012152.2:c.38T>C, NP_036284.1:p.Phe13Ser

Select item 144305213619.

rs1443052136 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:84813991 (GRCh38)
1:85279674 (GRCh37)
Canonical SPDI:: NC_000001.11:84813990:T:A
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.84813991T>A, NC_000001.10:g.85279674T>A, NM_012152.3:c.917A>T, NM_012152.2:c.917A>T, NP_036284.1:p.Lys306Met

Select item 144223534120.

rs1442235341 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:84865865 (GRCh38)
1:85331548 (GRCh37)
Canonical SPDI:: NC_000001.11:84865864:G:C
Gene:: LPAR3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.84865865G>C, NC_000001.10:g.85331548G>C, NM_012152.3:c.256C>G, NM_012152.2:c.256C>G, NP_036284.1:p.Leu86Val

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