SNP Links for Protein (Select 487439767) - SNP

Select item 14865275071.

rs1486527507 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:78755775 (GRCh38)
X:78011272 (GRCh37)
Canonical SPDI:: NC_000023.11:78755774:G:C
Gene:: LPAR4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000016/3 (GnomAD_exomes)
C=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.78755775G>C, NC_000023.10:g.78011272G>C, NG_013242.1:g.13067G>C, NM_001278000.3:c.906G>C, NM_001278000.2:c.906G>C, NM_001278000.1:c.906G>C, NM_005296.3:c.906G>C, NM_005296.2:c.906G>C, XM_006724639.4:c.906G>C, XM_006724639.3:c.906G>C, XM_006724639.2:c.906G>C, XM_006724639.1:c.906G>C, XM_017029437.2:c.906G>C, XM_017029437.1:c.906G>C, XM_017029438.2:c.906G>C, XM_017029438.1:c.906G>C, XM_047442015.1:c.906G>C, XM_047442013.1:c.906G>C, XM_047442011.1:c.906G>C, XM_047442012.1:c.906G>C, XM_047442014.1:c.906G>C

Select item 14859792732.

rs1485979273 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:78755927 (GRCh38)
X:78011424 (GRCh37)
Canonical SPDI:: NC_000023.11:78755926:T:C
Gene:: LPAR4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000006/1 (GnomAD_exomes)
C=0.000015/4 (TOPMED)
C=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.78755927T>C, NC_000023.10:g.78011424T>C, NG_013242.1:g.13219T>C, NM_001278000.3:c.1058T>C, NM_001278000.2:c.1058T>C, NM_001278000.1:c.1058T>C, NM_005296.3:c.1058T>C, NM_005296.2:c.1058T>C, XM_006724639.4:c.1058T>C, XM_006724639.3:c.1058T>C, XM_006724639.2:c.1058T>C, XM_006724639.1:c.1058T>C, XM_017029437.2:c.1058T>C, XM_017029437.1:c.1058T>C, XM_017029438.2:c.1058T>C, XM_017029438.1:c.1058T>C, XM_047442015.1:c.1058T>C, XM_047442013.1:c.1058T>C, XM_047442011.1:c.1058T>C, XM_047442012.1:c.1058T>C, XM_047442014.1:c.1058T>C, NP_001264929.1:p.Val353Ala, NP_005287.1:p.Val353Ala, XP_006724702.1:p.Val353Ala, XP_016884926.1:p.Val353Ala, XP_016884927.1:p.Val353Ala, XP_047297971.1:p.Val353Ala, XP_047297969.1:p.Val353Ala, XP_047297967.1:p.Val353Ala, XP_047297968.1:p.Val353Ala, XP_047297970.1:p.Val353Ala

Select item 14853666373.

rs1485366637 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:78755225 (GRCh38)
X:78010722 (GRCh37)
Canonical SPDI:: NC_000023.11:78755224:T:C
Gene:: LPAR4 (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=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.78755225T>C, NC_000023.10:g.78010722T>C, NG_013242.1:g.12517T>C, NM_001278000.3:c.356T>C, NM_001278000.2:c.356T>C, NM_001278000.1:c.356T>C, NM_005296.3:c.356T>C, NM_005296.2:c.356T>C, XM_006724639.4:c.356T>C, XM_006724639.3:c.356T>C, XM_006724639.2:c.356T>C, XM_006724639.1:c.356T>C, XM_017029437.2:c.356T>C, XM_017029437.1:c.356T>C, XM_017029438.2:c.356T>C, XM_017029438.1:c.356T>C, XM_047442015.1:c.356T>C, XM_047442013.1:c.356T>C, XM_047442011.1:c.356T>C, XM_047442012.1:c.356T>C, XM_047442014.1:c.356T>C, NP_001264929.1:p.Leu119Pro, NP_005287.1:p.Leu119Pro, XP_006724702.1:p.Leu119Pro, XP_016884926.1:p.Leu119Pro, XP_016884927.1:p.Leu119Pro, XP_047297971.1:p.Leu119Pro, XP_047297969.1:p.Leu119Pro, XP_047297967.1:p.Leu119Pro, XP_047297968.1:p.Leu119Pro, XP_047297970.1:p.Leu119Pro

Select item 14818280554.

rs1481828055 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:78755459 (GRCh38)
X:78010956 (GRCh37)
Canonical SPDI:: NC_000023.11:78755458:G:A
Gene:: LPAR4 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000223/2 (ALFA)
A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78755459G>A, NC_000023.10:g.78010956G>A, NG_013242.1:g.12751G>A, NM_001278000.3:c.590G>A, NM_001278000.2:c.590G>A, NM_001278000.1:c.590G>A, NM_005296.3:c.590G>A, NM_005296.2:c.590G>A, XM_006724639.4:c.590G>A, XM_006724639.3:c.590G>A, XM_006724639.2:c.590G>A, XM_006724639.1:c.590G>A, XM_017029437.2:c.590G>A, XM_017029437.1:c.590G>A, XM_017029438.2:c.590G>A, XM_017029438.1:c.590G>A, XM_047442015.1:c.590G>A, XM_047442013.1:c.590G>A, XM_047442011.1:c.590G>A, XM_047442012.1:c.590G>A, XM_047442014.1:c.590G>A, NP_001264929.1:p.Trp197Ter, NP_005287.1:p.Trp197Ter, XP_006724702.1:p.Trp197Ter, XP_016884926.1:p.Trp197Ter, XP_016884927.1:p.Trp197Ter, XP_047297971.1:p.Trp197Ter, XP_047297969.1:p.Trp197Ter, XP_047297967.1:p.Trp197Ter, XP_047297968.1:p.Trp197Ter, XP_047297970.1:p.Trp197Ter

Select item 14727382015.

rs1472738201 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:78755276 (GRCh38)
X:78010773 (GRCh37)
Canonical SPDI:: NC_000023.11:78755275:G:A
Gene:: LPAR4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78755276G>A, NC_000023.10:g.78010773G>A, NG_013242.1:g.12568G>A, NM_001278000.3:c.407G>A, NM_001278000.2:c.407G>A, NM_001278000.1:c.407G>A, NM_005296.3:c.407G>A, NM_005296.2:c.407G>A, XM_006724639.4:c.407G>A, XM_006724639.3:c.407G>A, XM_006724639.2:c.407G>A, XM_006724639.1:c.407G>A, XM_017029437.2:c.407G>A, XM_017029437.1:c.407G>A, XM_017029438.2:c.407G>A, XM_017029438.1:c.407G>A, XM_047442015.1:c.407G>A, XM_047442013.1:c.407G>A, XM_047442011.1:c.407G>A, XM_047442012.1:c.407G>A, XM_047442014.1:c.407G>A, NP_001264929.1:p.Arg136His, NP_005287.1:p.Arg136His, XP_006724702.1:p.Arg136His, XP_016884926.1:p.Arg136His, XP_016884927.1:p.Arg136His, XP_047297971.1:p.Arg136His, XP_047297969.1:p.Arg136His, XP_047297967.1:p.Arg136His, XP_047297968.1:p.Arg136His, XP_047297970.1:p.Arg136His

Select item 14710516746.

rs1471051674 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: X:78755089 (GRCh38)
X:78010586 (GRCh37)
Canonical SPDI:: NC_000023.11:78755088:A:G,NC_000023.11:78755088:A:T
Gene:: LPAR4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
T=0.000208/1 (1000Genomes)
HGVS:: NC_000023.11:g.78755089A>G, NC_000023.11:g.78755089A>T, NC_000023.10:g.78010586A>G, NC_000023.10:g.78010586A>T, NG_013242.1:g.12381A>G, NG_013242.1:g.12381A>T, NM_001278000.3:c.220A>G, NM_001278000.3:c.220A>T, NM_001278000.2:c.220A>G, NM_001278000.2:c.220A>T, NM_001278000.1:c.220A>G, NM_001278000.1:c.220A>T, NM_005296.3:c.220A>G, NM_005296.3:c.220A>T, NM_005296.2:c.220A>G, NM_005296.2:c.220A>T, XM_006724639.4:c.220A>G, XM_006724639.4:c.220A>T, XM_006724639.3:c.220A>G, XM_006724639.3:c.220A>T, XM_006724639.2:c.220A>G, XM_006724639.2:c.220A>T, XM_006724639.1:c.220A>G, XM_006724639.1:c.220A>T, XM_017029437.2:c.220A>G, XM_017029437.2:c.220A>T, XM_017029437.1:c.220A>G, XM_017029437.1:c.220A>T, XM_017029438.2:c.220A>G, XM_017029438.2:c.220A>T, XM_017029438.1:c.220A>G, XM_017029438.1:c.220A>T, XM_047442015.1:c.220A>G, XM_047442015.1:c.220A>T, XM_047442013.1:c.220A>G, XM_047442013.1:c.220A>T, XM_047442011.1:c.220A>G, XM_047442011.1:c.220A>T, XM_047442012.1:c.220A>G, XM_047442012.1:c.220A>T, XM_047442014.1:c.220A>G, XM_047442014.1:c.220A>T, NP_001264929.1:p.Thr74Ala, NP_001264929.1:p.Thr74Ser, NP_005287.1:p.Thr74Ala, NP_005287.1:p.Thr74Ser, XP_006724702.1:p.Thr74Ala, XP_006724702.1:p.Thr74Ser, XP_016884926.1:p.Thr74Ala, XP_016884926.1:p.Thr74Ser, XP_016884927.1:p.Thr74Ala, XP_016884927.1:p.Thr74Ser, XP_047297971.1:p.Thr74Ala, XP_047297971.1:p.Thr74Ser, XP_047297969.1:p.Thr74Ala, XP_047297969.1:p.Thr74Ser, XP_047297967.1:p.Thr74Ala, XP_047297967.1:p.Thr74Ser, XP_047297968.1:p.Thr74Ala, XP_047297968.1:p.Thr74Ser, XP_047297970.1:p.Thr74Ala, XP_047297970.1:p.Thr74Ser

Select item 14634432157.

rs1463443215 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:78755525 (GRCh38)
X:78011022 (GRCh37)
Canonical SPDI:: NC_000023.11:78755524:T:C
Gene:: LPAR4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000005/1 (GnomAD_exomes)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.78755525T>C, NC_000023.10:g.78011022T>C, NG_013242.1:g.12817T>C, NM_001278000.3:c.656T>C, NM_001278000.2:c.656T>C, NM_001278000.1:c.656T>C, NM_005296.3:c.656T>C, NM_005296.2:c.656T>C, XM_006724639.4:c.656T>C, XM_006724639.3:c.656T>C, XM_006724639.2:c.656T>C, XM_006724639.1:c.656T>C, XM_017029437.2:c.656T>C, XM_017029437.1:c.656T>C, XM_017029438.2:c.656T>C, XM_017029438.1:c.656T>C, XM_047442015.1:c.656T>C, XM_047442013.1:c.656T>C, XM_047442011.1:c.656T>C, XM_047442012.1:c.656T>C, XM_047442014.1:c.656T>C, NP_001264929.1:p.Leu219Ser, NP_005287.1:p.Leu219Ser, XP_006724702.1:p.Leu219Ser, XP_016884926.1:p.Leu219Ser, XP_016884927.1:p.Leu219Ser, XP_047297971.1:p.Leu219Ser, XP_047297969.1:p.Leu219Ser, XP_047297967.1:p.Leu219Ser, XP_047297968.1:p.Leu219Ser, XP_047297970.1:p.Leu219Ser

Select item 14617075908.

rs1461707590 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:78755670 (GRCh38)
X:78011167 (GRCh37)
Canonical SPDI:: NC_000023.11:78755669:T:C
Gene:: LPAR4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0.000111/1 (ALFA)
C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78755670T>C, NC_000023.10:g.78011167T>C, NG_013242.1:g.12962T>C, NM_001278000.3:c.801T>C, NM_001278000.2:c.801T>C, NM_001278000.1:c.801T>C, NM_005296.3:c.801T>C, NM_005296.2:c.801T>C, XM_006724639.4:c.801T>C, XM_006724639.3:c.801T>C, XM_006724639.2:c.801T>C, XM_006724639.1:c.801T>C, XM_017029437.2:c.801T>C, XM_017029437.1:c.801T>C, XM_017029438.2:c.801T>C, XM_017029438.1:c.801T>C, XM_047442015.1:c.801T>C, XM_047442013.1:c.801T>C, XM_047442011.1:c.801T>C, XM_047442012.1:c.801T>C, XM_047442014.1:c.801T>C

Select item 14610610479.

rs1461061047 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:78755485 (GRCh38)
X:78010982 (GRCh37)
Canonical SPDI:: NC_000023.11:78755484:A:G
Gene:: LPAR4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.78755485A>G, NC_000023.10:g.78010982A>G, NG_013242.1:g.12777A>G, NM_001278000.3:c.616A>G, NM_001278000.2:c.616A>G, NM_001278000.1:c.616A>G, NM_005296.3:c.616A>G, NM_005296.2:c.616A>G, XM_006724639.4:c.616A>G, XM_006724639.3:c.616A>G, XM_006724639.2:c.616A>G, XM_006724639.1:c.616A>G, XM_017029437.2:c.616A>G, XM_017029437.1:c.616A>G, XM_017029438.2:c.616A>G, XM_017029438.1:c.616A>G, XM_047442015.1:c.616A>G, XM_047442013.1:c.616A>G, XM_047442011.1:c.616A>G, XM_047442012.1:c.616A>G, XM_047442014.1:c.616A>G, NP_001264929.1:p.Ile206Val, NP_005287.1:p.Ile206Val, XP_006724702.1:p.Ile206Val, XP_016884926.1:p.Ile206Val, XP_016884927.1:p.Ile206Val, XP_047297971.1:p.Ile206Val, XP_047297969.1:p.Ile206Val, XP_047297967.1:p.Ile206Val, XP_047297968.1:p.Ile206Val, XP_047297970.1:p.Ile206Val

Select item 146071719610.

rs1460717196 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:78755730 (GRCh38)
X:78011227 (GRCh37)
Canonical SPDI:: NC_000023.11:78755729:A:G
Gene:: LPAR4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.78755730A>G, NC_000023.10:g.78011227A>G, NG_013242.1:g.13022A>G, NM_001278000.3:c.861A>G, NM_001278000.2:c.861A>G, NM_001278000.1:c.861A>G, NM_005296.3:c.861A>G, NM_005296.2:c.861A>G, XM_006724639.4:c.861A>G, XM_006724639.3:c.861A>G, XM_006724639.2:c.861A>G, XM_006724639.1:c.861A>G, XM_017029437.2:c.861A>G, XM_017029437.1:c.861A>G, XM_017029438.2:c.861A>G, XM_017029438.1:c.861A>G, XM_047442015.1:c.861A>G, XM_047442013.1:c.861A>G, XM_047442011.1:c.861A>G, XM_047442012.1:c.861A>G, XM_047442014.1:c.861A>G

Select item 145846826411.

rs1458468264 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:78755826 (GRCh38)
X:78011323 (GRCh37)
Canonical SPDI:: NC_000023.11:78755825:G:A
Gene:: LPAR4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000023.11:g.78755826G>A, NC_000023.10:g.78011323G>A, NG_013242.1:g.13118G>A, NM_001278000.3:c.957G>A, NM_001278000.2:c.957G>A, NM_001278000.1:c.957G>A, NM_005296.3:c.957G>A, NM_005296.2:c.957G>A, XM_006724639.4:c.957G>A, XM_006724639.3:c.957G>A, XM_006724639.2:c.957G>A, XM_006724639.1:c.957G>A, XM_017029437.2:c.957G>A, XM_017029437.1:c.957G>A, XM_017029438.2:c.957G>A, XM_017029438.1:c.957G>A, XM_047442015.1:c.957G>A, XM_047442013.1:c.957G>A, XM_047442011.1:c.957G>A, XM_047442012.1:c.957G>A, XM_047442014.1:c.957G>A

Select item 145601722512.

rs1456017225 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:78755802 (GRCh38)
X:78011299 (GRCh37)
Canonical SPDI:: NC_000023.11:78755801:T:C
Gene:: LPAR4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.78755802T>C, NC_000023.10:g.78011299T>C, NG_013242.1:g.13094T>C, NM_001278000.3:c.933T>C, NM_001278000.2:c.933T>C, NM_001278000.1:c.933T>C, NM_005296.3:c.933T>C, NM_005296.2:c.933T>C, XM_006724639.4:c.933T>C, XM_006724639.3:c.933T>C, XM_006724639.2:c.933T>C, XM_006724639.1:c.933T>C, XM_017029437.2:c.933T>C, XM_017029437.1:c.933T>C, XM_017029438.2:c.933T>C, XM_017029438.1:c.933T>C, XM_047442015.1:c.933T>C, XM_047442013.1:c.933T>C, XM_047442011.1:c.933T>C, XM_047442012.1:c.933T>C, XM_047442014.1:c.933T>C

Select item 144965848613.

rs1449658486 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:78754896 (GRCh38)
X:78010393 (GRCh37)
Canonical SPDI:: NC_000023.11:78754895:C:T
Gene:: LPAR4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.00001/1 (GnomAD)
T=0.000012/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78754896C>T, NC_000023.10:g.78010393C>T, NG_013242.1:g.12188C>T, NM_001278000.3:c.27C>T, NM_001278000.2:c.27C>T, NM_001278000.1:c.27C>T, NM_005296.3:c.27C>T, NM_005296.2:c.27C>T, XM_006724639.4:c.27C>T, XM_006724639.3:c.27C>T, XM_006724639.2:c.27C>T, XM_006724639.1:c.27C>T, XM_017029437.2:c.27C>T, XM_017029437.1:c.27C>T, XM_017029438.2:c.27C>T, XM_017029438.1:c.27C>T, XM_047442015.1:c.27C>T, XM_047442013.1:c.27C>T, XM_047442011.1:c.27C>T, XM_047442012.1:c.27C>T, XM_047442014.1:c.27C>T

Select item 144726832814.

rs1447268328 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:78755128 (GRCh38)
X:78010625 (GRCh37)
Canonical SPDI:: NC_000023.11:78755127:C:A
Gene:: LPAR4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000011/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.78755128C>A, NC_000023.10:g.78010625C>A, NG_013242.1:g.12420C>A, NM_001278000.3:c.259C>A, NM_001278000.2:c.259C>A, NM_001278000.1:c.259C>A, NM_005296.3:c.259C>A, NM_005296.2:c.259C>A, XM_006724639.4:c.259C>A, XM_006724639.3:c.259C>A, XM_006724639.2:c.259C>A, XM_006724639.1:c.259C>A, XM_017029437.2:c.259C>A, XM_017029437.1:c.259C>A, XM_017029438.2:c.259C>A, XM_017029438.1:c.259C>A, XM_047442015.1:c.259C>A, XM_047442013.1:c.259C>A, XM_047442011.1:c.259C>A, XM_047442012.1:c.259C>A, XM_047442014.1:c.259C>A, NP_001264929.1:p.Leu87Ile, NP_005287.1:p.Leu87Ile, XP_006724702.1:p.Leu87Ile, XP_016884926.1:p.Leu87Ile, XP_016884927.1:p.Leu87Ile, XP_047297971.1:p.Leu87Ile, XP_047297969.1:p.Leu87Ile, XP_047297967.1:p.Leu87Ile, XP_047297968.1:p.Leu87Ile, XP_047297970.1:p.Leu87Ile

Select item 144706245715.

rs1447062457 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:78755508 (GRCh38)
X:78011005 (GRCh37)
Canonical SPDI:: NC_000023.11:78755507:T:C
Gene:: LPAR4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000005/1 (GnomAD_exomes)
C=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.78755508T>C, NC_000023.10:g.78011005T>C, NG_013242.1:g.12800T>C, NM_001278000.3:c.639T>C, NM_001278000.2:c.639T>C, NM_001278000.1:c.639T>C, NM_005296.3:c.639T>C, NM_005296.2:c.639T>C, XM_006724639.4:c.639T>C, XM_006724639.3:c.639T>C, XM_006724639.2:c.639T>C, XM_006724639.1:c.639T>C, XM_017029437.2:c.639T>C, XM_017029437.1:c.639T>C, XM_017029438.2:c.639T>C, XM_017029438.1:c.639T>C, XM_047442015.1:c.639T>C, XM_047442013.1:c.639T>C, XM_047442011.1:c.639T>C, XM_047442012.1:c.639T>C, XM_047442014.1:c.639T>C

Select item 144327573316.

rs1443275733 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:78755144 (GRCh38)
X:78010641 (GRCh37)
Canonical SPDI:: NC_000023.11:78755143:T:C
Gene:: LPAR4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.78755144T>C, NC_000023.10:g.78010641T>C, NG_013242.1:g.12436T>C, NM_001278000.3:c.275T>C, NM_001278000.2:c.275T>C, NM_001278000.1:c.275T>C, NM_005296.3:c.275T>C, NM_005296.2:c.275T>C, XM_006724639.4:c.275T>C, XM_006724639.3:c.275T>C, XM_006724639.2:c.275T>C, XM_006724639.1:c.275T>C, XM_017029437.2:c.275T>C, XM_017029437.1:c.275T>C, XM_017029438.2:c.275T>C, XM_017029438.1:c.275T>C, XM_047442015.1:c.275T>C, XM_047442013.1:c.275T>C, XM_047442011.1:c.275T>C, XM_047442012.1:c.275T>C, XM_047442014.1:c.275T>C, NP_001264929.1:p.Leu92Pro, NP_005287.1:p.Leu92Pro, XP_006724702.1:p.Leu92Pro, XP_016884926.1:p.Leu92Pro, XP_016884927.1:p.Leu92Pro, XP_047297971.1:p.Leu92Pro, XP_047297969.1:p.Leu92Pro, XP_047297967.1:p.Leu92Pro, XP_047297968.1:p.Leu92Pro, XP_047297970.1:p.Leu92Pro

Select item 143994888617.

rs1439948886 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: X:78755899 (GRCh38)
X:78011396 (GRCh37)
Canonical SPDI:: NC_000023.11:78755898:CC:C
Gene:: LPAR4 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.78755900del, NC_000023.10:g.78011397del, NG_013242.1:g.13192del, NM_001278000.3:c.1031del, NM_001278000.2:c.1031del, NM_001278000.1:c.1031del, NM_005296.3:c.1031del, NM_005296.2:c.1031del, XM_006724639.4:c.1031del, XM_006724639.3:c.1031del, XM_006724639.2:c.1031del, XM_006724639.1:c.1031del, XM_017029437.2:c.1031del, XM_017029437.1:c.1031del, XM_017029438.2:c.1031del, XM_017029438.1:c.1031del, XM_047442015.1:c.1031del, XM_047442013.1:c.1031del, XM_047442011.1:c.1031del, XM_047442012.1:c.1031del, XM_047442014.1:c.1031del, NP_001264929.1:p.Pro344fs, NP_005287.1:p.Pro344fs, XP_006724702.1:p.Pro344fs, XP_016884926.1:p.Pro344fs, XP_016884927.1:p.Pro344fs, XP_047297971.1:p.Pro344fs, XP_047297969.1:p.Pro344fs, XP_047297967.1:p.Pro344fs, XP_047297968.1:p.Pro344fs, XP_047297970.1:p.Pro344fs

Select item 143663696318.

rs1436636963 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:78755945 (GRCh38)
X:78011442 (GRCh37)
Canonical SPDI:: NC_000023.11:78755944:A:G
Gene:: LPAR4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.78755945A>G, NC_000023.10:g.78011442A>G, NG_013242.1:g.13237A>G, NM_001278000.3:c.1076A>G, NM_001278000.2:c.1076A>G, NM_001278000.1:c.1076A>G, NM_005296.3:c.1076A>G, NM_005296.2:c.1076A>G, XM_006724639.4:c.1076A>G, XM_006724639.3:c.1076A>G, XM_006724639.2:c.1076A>G, XM_006724639.1:c.1076A>G, XM_017029437.2:c.1076A>G, XM_017029437.1:c.1076A>G, XM_017029438.2:c.1076A>G, XM_017029438.1:c.1076A>G, XM_047442015.1:c.1076A>G, XM_047442013.1:c.1076A>G, XM_047442011.1:c.1076A>G, XM_047442012.1:c.1076A>G, XM_047442014.1:c.1076A>G, NP_001264929.1:p.Asn359Ser, NP_005287.1:p.Asn359Ser, XP_006724702.1:p.Asn359Ser, XP_016884926.1:p.Asn359Ser, XP_016884927.1:p.Asn359Ser, XP_047297971.1:p.Asn359Ser, XP_047297969.1:p.Asn359Ser, XP_047297967.1:p.Asn359Ser, XP_047297968.1:p.Asn359Ser, XP_047297970.1:p.Asn359Ser

Select item 143226834419.

rs1432268344 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:78755455 (GRCh38)
X:78010952 (GRCh37)
Canonical SPDI:: NC_000023.11:78755454:G:T
Gene:: LPAR4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.78755455G>T, NC_000023.10:g.78010952G>T, NG_013242.1:g.12747G>T, NM_001278000.3:c.586G>T, NM_001278000.2:c.586G>T, NM_001278000.1:c.586G>T, NM_005296.3:c.586G>T, NM_005296.2:c.586G>T, XM_006724639.4:c.586G>T, XM_006724639.3:c.586G>T, XM_006724639.2:c.586G>T, XM_006724639.1:c.586G>T, XM_017029437.2:c.586G>T, XM_017029437.1:c.586G>T, XM_017029438.2:c.586G>T, XM_017029438.1:c.586G>T, XM_047442015.1:c.586G>T, XM_047442013.1:c.586G>T, XM_047442011.1:c.586G>T, XM_047442012.1:c.586G>T, XM_047442014.1:c.586G>T, NP_001264929.1:p.Val196Phe, NP_005287.1:p.Val196Phe, XP_006724702.1:p.Val196Phe, XP_016884926.1:p.Val196Phe, XP_016884927.1:p.Val196Phe, XP_047297971.1:p.Val196Phe, XP_047297969.1:p.Val196Phe, XP_047297967.1:p.Val196Phe, XP_047297968.1:p.Val196Phe, XP_047297970.1:p.Val196Phe

Select item 142034192520.

rs1420341925 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:78755351 (GRCh38)
X:78010848 (GRCh37)
Canonical SPDI:: NC_000023.11:78755350:G:C
Gene:: LPAR4 (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_000023.11:g.78755351G>C, NC_000023.10:g.78010848G>C, NG_013242.1:g.12643G>C, NM_001278000.3:c.482G>C, NM_001278000.2:c.482G>C, NM_001278000.1:c.482G>C, NM_005296.3:c.482G>C, NM_005296.2:c.482G>C, XM_006724639.4:c.482G>C, XM_006724639.3:c.482G>C, XM_006724639.2:c.482G>C, XM_006724639.1:c.482G>C, XM_017029437.2:c.482G>C, XM_017029437.1:c.482G>C, XM_017029438.2:c.482G>C, XM_017029438.1:c.482G>C, XM_047442015.1:c.482G>C, XM_047442013.1:c.482G>C, XM_047442011.1:c.482G>C, XM_047442012.1:c.482G>C, XM_047442014.1:c.482G>C, NP_001264929.1:p.Gly161Ala, NP_005287.1:p.Gly161Ala, XP_006724702.1:p.Gly161Ala, XP_016884926.1:p.Gly161Ala, XP_016884927.1:p.Gly161Ala, XP_047297971.1:p.Gly161Ala, XP_047297969.1:p.Gly161Ala, XP_047297967.1:p.Gly161Ala, XP_047297968.1:p.Gly161Ala, XP_047297970.1:p.Gly161Ala

dbSNP

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dbSNP

Result Filters

Clinical Significance

Validation Status

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Global MAF

Custom range

Additional filters

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Items: 1 to 20 of 234

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