SNP Links for Protein (Select 307691233) - SNP

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Links from Protein

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Select item 14881519631.

rs1488151963 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:93587459 (GRCh38)
10:95347216 (GRCh37)
Canonical SPDI:: NC_000010.11:93587458:T:C
Gene:: FFAR4 (Varview)
Functional Consequence:: synonymous_variant,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.93587459T>C, NC_000010.10:g.95347216T>C, NG_032670.1:g.25795T>C, NM_181745.4:c.984T>C, NM_181745.3:c.984T>C, NM_001195755.2:c.936T>C, NM_001195755.1:c.936T>C

Select item 14865710002.

rs1486571000 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:93566901 (GRCh38)
10:95326658 (GRCh37)
Canonical SPDI:: NC_000010.11:93566900:G:T
Gene:: FFAR4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.93566901G>T, NC_000010.10:g.95326658G>T, NG_032670.1:g.5237G>T, NM_181745.4:c.181G>T, NM_181745.3:c.181G>T, NM_001195755.2:c.181G>T, NM_001195755.1:c.181G>T, XM_011539746.4:c.181G>T, XM_011539746.3:c.181G>T, XM_011539746.2:c.181G>T, XM_011539746.1:c.181G>T, NP_859529.2:p.Ala61Ser, NP_001182684.1:p.Ala61Ser, XP_011538048.1:p.Ala61Ser

Select item 14860510983.

rs1486051098 [Homo sapiens]

Variant type:: DELINS
Alleles:: AC>- [Show Flanks]
Chromosome:: 10:93576108 (GRCh38)
10:95335865 (GRCh37)
Canonical SPDI:: NC_000010.11:93576104:CACAC:CAC
Gene:: FFAR4 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: -=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000010.11:g.93576106AC[1], NC_000010.10:g.95335863AC[1], NG_032670.1:g.14442AC[1], NM_181745.4:c.585_586del, NM_181745.3:c.585_586del, NM_001195755.2:c.585_586del, NM_001195755.1:c.585_586del, XM_011539746.4:c.585_586del, XM_011539746.3:c.585_586del, XM_011539746.2:c.585_586del, XM_011539746.1:c.585_586del, NP_859529.2:p.Leu196fs, NP_001182684.1:p.Leu196fs, XP_011538048.1:p.Leu196fs

Select item 14840832644.

rs1484083264 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:93587554 (GRCh38)
10:95347311 (GRCh37)
Canonical SPDI:: NC_000010.11:93587553:C:G,NC_000010.11:93587553:C:T
Gene:: FFAR4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.93587554C>G, NC_000010.11:g.93587554C>T, NC_000010.10:g.95347311C>G, NC_000010.10:g.95347311C>T, NG_032670.1:g.25890C>G, NG_032670.1:g.25890C>T, NM_181745.4:c.1079C>G, NM_181745.4:c.1079C>T, NM_181745.3:c.1079C>G, NM_181745.3:c.1079C>T, NM_001195755.2:c.1031C>G, NM_001195755.2:c.1031C>T, NM_001195755.1:c.1031C>G, NM_001195755.1:c.1031C>T, NP_859529.2:p.Ala360Gly, NP_859529.2:p.Ala360Val, NP_001182684.1:p.Ala344Gly, NP_001182684.1:p.Ala344Val

Select item 14824527615.

rs1482452761 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:93587227 (GRCh38)
10:95346984 (GRCh37)
Canonical SPDI:: NC_000010.11:93587226:A:G
Gene:: FFAR4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_downstream_transcript_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_000010.11:g.93587227A>G, NC_000010.10:g.95346984A>G, NG_032670.1:g.25563A>G, NM_181745.4:c.752A>G, NM_181745.3:c.752A>G, NM_001195755.2:c.704A>G, NM_001195755.1:c.704A>G, NP_859529.2:p.Lys251Arg, NP_001182684.1:p.Lys235Arg

Select item 14811790976.

rs1481179097 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:93567131 (GRCh38)
10:95326888 (GRCh37)
Canonical SPDI:: NC_000010.11:93567130:G:T
Gene:: FFAR4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.93567131G>T, NC_000010.10:g.95326888G>T, NG_032670.1:g.5467G>T, NM_181745.4:c.411G>T, NM_181745.3:c.411G>T, NM_001195755.2:c.411G>T, NM_001195755.1:c.411G>T, XM_011539746.4:c.411G>T, XM_011539746.3:c.411G>T, XM_011539746.2:c.411G>T, XM_011539746.1:c.411G>T, NP_859529.2:p.Met137Ile, NP_001182684.1:p.Met137Ile, XP_011538048.1:p.Met137Ile

Select item 14750488127.

rs1475048812 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 10:93567123 (GRCh38)
10:95326881 (GRCh37)
Canonical SPDI:: NC_000010.11:93567123:A:AA
Gene:: FFAR4 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.93567124dup, NC_000010.10:g.95326881dup, NG_032670.1:g.5460dup, NM_181745.4:c.404dup, NM_181745.3:c.404dup, NM_001195755.2:c.404dup, NM_001195755.1:c.404dup, XM_011539746.4:c.404dup, XM_011539746.3:c.404dup, XM_011539746.2:c.404dup, XM_011539746.1:c.404dup, NP_859529.2:p.Arg136fs, NP_001182684.1:p.Arg136fs, XP_011538048.1:p.Arg136fs

Select item 14733409098.

rs1473340909 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:93567186 (GRCh38)
10:95326943 (GRCh37)
Canonical SPDI:: NC_000010.11:93567185:G:C
Gene:: FFAR4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.93567186G>C, NC_000010.10:g.95326943G>C, NG_032670.1:g.5522G>C, NM_181745.4:c.466G>C, NM_181745.3:c.466G>C, NM_001195755.2:c.466G>C, NM_001195755.1:c.466G>C, XM_011539746.4:c.466G>C, XM_011539746.3:c.466G>C, XM_011539746.2:c.466G>C, XM_011539746.1:c.466G>C, NP_859529.2:p.Ala156Pro, NP_001182684.1:p.Ala156Pro, XP_011538048.1:p.Ala156Pro

Select item 14719875939.

rs1471987593 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 10:93567093 (GRCh38)
10:95326850 (GRCh37)
Canonical SPDI:: NC_000010.11:93567092:A:T
Gene:: FFAR4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000010.11:g.93567093A>T, NC_000010.10:g.95326850A>T, NG_032670.1:g.5429A>T, NM_181745.4:c.373A>T, NM_181745.3:c.373A>T, NM_001195755.2:c.373A>T, NM_001195755.1:c.373A>T, XM_011539746.4:c.373A>T, XM_011539746.3:c.373A>T, XM_011539746.2:c.373A>T, XM_011539746.1:c.373A>T, NP_859529.2:p.Thr125Ser, NP_001182684.1:p.Thr125Ser, XP_011538048.1:p.Thr125Ser

Select item 147163941810.

rs1471639418 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:93587306 (GRCh38)
10:95347063 (GRCh37)
Canonical SPDI:: NC_000010.11:93587305:G:A
Gene:: FFAR4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.93587306G>A, NC_000010.10:g.95347063G>A, NG_032670.1:g.25642G>A, NM_181745.4:c.831G>A, NM_181745.3:c.831G>A, NM_001195755.2:c.783G>A, NM_001195755.1:c.783G>A