SNP Links for Gene (Select 2865) - SNP

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Select item 14914738601.

rs1491473860 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 19:35356352 (GRCh38)
19:35847254 (GRCh37)
Canonical SPDI:: NC_000019.10:35356350:TGT:T
Gene:: FFAR3 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.07613/903 (ALFA)
-=0.08828/7596 (GnomAD)
-=0.15784/2566 (TOMMO)
HGVS:: NC_000019.10:g.35356352_35356353del, NC_000019.9:g.35847254_35847255del

Select item 14912852852.

rs1491285285 has merged into rs59244534 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTT>-,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 19:35356550 (GRCh38)
19:35847452 (GRCh37)
Canonical SPDI:: NC_000019.10:35356543:TTTTTTTTTTTTTTTT:TTTTTT,NC_000019.10:35356543:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000019.10:35356543:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000019.10:35356543:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000019.10:35356543:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:35356543:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:35356543:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000019.10:35356543:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000019.10:35356543:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35356543:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35356543:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: FFAR3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.223842/1121 (1000Genomes)
HGVS:: NC_000019.10:g.35356550_35356559del, NC_000019.10:g.35356555_35356559del, NC_000019.10:g.35356556_35356559del, NC_000019.10:g.35356557_35356559del, NC_000019.10:g.35356558_35356559del, NC_000019.10:g.35356559del, NC_000019.10:g.35356559dup, NC_000019.10:g.35356558_35356559dup, NC_000019.10:g.35356553_35356559dup, NC_000019.10:g.35356551_35356559dup, NC_000019.10:g.35356545_35356559dup, NC_000019.9:g.35847452_35847461del, NC_000019.9:g.35847457_35847461del, NC_000019.9:g.35847458_35847461del, NC_000019.9:g.35847459_35847461del, NC_000019.9:g.35847460_35847461del, NC_000019.9:g.35847461del, NC_000019.9:g.35847461dup, NC_000019.9:g.35847460_35847461dup, NC_000019.9:g.35847455_35847461dup, NC_000019.9:g.35847453_35847461dup, NC_000019.9:g.35847447_35847461dup

Select item 14907574423.

rs1490757442 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:35360103 (GRCh38)
19:35851005 (GRCh37)
Canonical SPDI:: NC_000019.10:35360102:C:T
Gene:: FFAR3 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.35360103C>T, NC_000019.9:g.35851005C>T, NM_005304.5:c.*172C>T, NM_005304.4:c.*172C>T, NM_005304.3:c.*172C>T, XM_011526858.3:c.*172C>T, XM_011526858.2:c.*172C>T, XM_011526858.1:c.*172C>T

Select item 14905915144.

rs1490591514 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:35360537 (GRCh38)
19:35851439 (GRCh37)
Canonical SPDI:: NC_000019.10:35360536:G:C
Gene:: FFAR3 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000019.10:g.35360537G>C, NC_000019.9:g.35851439G>C

Select item 14899760585.

rs1489976058 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:35360145 (GRCh38)
19:35851047 (GRCh37)
Canonical SPDI:: NC_000019.10:35360144:G:C
Gene:: FFAR3 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.35360145G>C, NC_000019.9:g.35851047G>C, NM_005304.5:c.*214G>C, NM_005304.4:c.*214G>C, NM_005304.3:c.*214G>C, XM_011526858.3:c.*214G>C, XM_011526858.2:c.*214G>C, XM_011526858.1:c.*214G>C

Select item 14899290046.

rs1489929004 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TGAC [Show Flanks]
Chromosome:: 19:35358746 (GRCh38)
19:35849649 (GRCh37)
Canonical SPDI:: NC_000019.10:35358746:CTGAC:CTGACTGAC
Gene:: FFAR3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTGACTGAC=0.000084/1 (ALFA)
CTGA=0.000058/8 (GnomAD)
CTGA=0.000238/63 (TOPMED)
CTGA=0.002407/40 (TOMMO)
HGVS:: NC_000019.10:g.35358748_35358751dup, NC_000019.9:g.35849650_35849653dup

Select item 14892428417.

rs1489242841 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 19:35359420 (GRCh38)
19:35850322 (GRCh37)
Canonical SPDI:: NC_000019.10:35359419:A:T
Gene:: FFAR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.35359420A>T, NC_000019.9:g.35850322A>T, NM_005304.5:c.530A>T, NM_005304.4:c.530A>T, NM_005304.3:c.530A>T, XM_011526858.3:c.641A>T, XM_011526858.2:c.641A>T, XM_011526858.1:c.641A>T, NP_005295.1:p.Gln177Leu, XP_011525160.1:p.Gln214Leu

Select item 14892300038.

rs1489230003 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 19:35359250 (GRCh38)
19:35850152 (GRCh37)
Canonical SPDI:: NC_000019.10:35359249:A:
Gene:: FFAR3 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
HGVS:: NC_000019.10:g.35359250del, NC_000019.9:g.35850152del, NM_005304.5:c.360del, NM_005304.4:c.360del, NM_005304.3:c.360del, XM_011526858.3:c.471del, XM_011526858.2:c.471del, XM_011526858.1:c.471del, NP_005295.1:p.Leu121fs, XP_011525160.1:p.Leu158fs

Select item 14890804129.

rs1489080412 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 19:35357875 (GRCh38)
19:35848777 (GRCh37)
Canonical SPDI:: NC_000019.10:35357874:G:A,NC_000019.10:35357874:G:T
Gene:: FFAR3 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0./0 (GnomAD)
A=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.35357875G>A, NC_000019.10:g.35357875G>T, NC_000019.9:g.35848777G>A, NC_000019.9:g.35848777G>T

Select item 148866982410.

rs1488669824 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 19:35356911 (GRCh38)
19:35847814 (GRCh37)
Canonical SPDI:: NC_000019.10:35356911::G
Gene:: FFAR3 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.35356911_35356912insG, NC_000019.9:g.35847813_35847814insG

Select item 148859775711.

rs1488597757 has merged into rs1023459493 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>-,CC [Show Flanks]
Chromosome:: 19:35356279 (GRCh38)
19:35847181 (GRCh37)
Canonical SPDI:: NC_000019.10:35356278:CCCCC:CCCC,NC_000019.10:35356278:CCCCC:CCCCCC
Gene:: FFAR3 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCCCCC=0./0 (ALFA)
HGVS:: NC_000019.10:g.35356283del, NC_000019.10:g.35356283dup, NC_000019.9:g.35847185del, NC_000019.9:g.35847185dup

Select item 148827346512.

rs1488273465 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:35356436 (GRCh38)
19:35847338 (GRCh37)
Canonical SPDI:: NC_000019.10:35356435:C:T
Gene:: FFAR3 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.35356436C>T, NC_000019.9:g.35847338C>T

Select item 148810077413.

rs1488100774 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:35356932 (GRCh38)
19:35847834 (GRCh37)
Canonical SPDI:: NC_000019.10:35356931:C:T
Gene:: FFAR3 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000019/5 (TOPMED)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000019.10:g.35356932C>T, NC_000019.9:g.35847834C>T

Select item 148723964314.

rs1487239643 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:35359691 (GRCh38)
19:35850593 (GRCh37)
Canonical SPDI:: NC_000019.10:35359690:G:A
Gene:: FFAR3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.35359691G>A, NC_000019.9:g.35850593G>A, NM_005304.5:c.801G>A, NM_005304.4:c.801G>A, NM_005304.3:c.801G>A, XM_011526858.3:c.912G>A, XM_011526858.2:c.912G>A, XM_011526858.1:c.912G>A

Select item 148721389215.

rs1487213892 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:35359222 (GRCh38)
19:35850124 (GRCh37)
Canonical SPDI:: NC_000019.10:35359221:T:C
Gene:: FFAR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.35359222T>C, NC_000019.9:g.35850124T>C, NM_005304.5:c.332T>C, NM_005304.4:c.332T>C, NM_005304.3:c.332T>C, XM_011526858.3:c.443T>C, XM_011526858.2:c.443T>C, XM_011526858.1:c.443T>C, NP_005295.1:p.Ile111Thr, XP_011525160.1:p.Ile148Thr

Select item 148706636416.

rs1487066364 has merged into rs61276188 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 19:35357166 (GRCh38)
19:35848068 (GRCh37)
Canonical SPDI:: NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35357155:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: FFAR3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000019.10:g.35357166_35357180del, NC_000019.10:g.35357168_35357180del, NC_000019.10:g.35357169_35357180del, NC_000019.10:g.35357170_35357180del, NC_000019.10:g.35357171_35357180del, NC_000019.10:g.35357172_35357180del, NC_000019.10:g.35357173_35357180del, NC_000019.10:g.35357174_35357180del, NC_000019.10:g.35357175_35357180del, NC_000019.10:g.35357176_35357180del, NC_000019.10:g.35357177_35357180del, NC_000019.10:g.35357178_35357180del, NC_000019.10:g.35357179_35357180del, NC_000019.10:g.35357180del, NC_000019.10:g.35357180dup, NC_000019.10:g.35357179_35357180dup, NC_000019.10:g.35357178_35357180dup, NC_000019.10:g.35357177_35357180dup, NC_000019.10:g.35357176_35357180dup, NC_000019.10:g.35357175_35357180dup, NC_000019.10:g.35357174_35357180dup, NC_000019.10:g.35357173_35357180dup, NC_000019.10:g.35357172_35357180dup, NC_000019.10:g.35357171_35357180dup, NC_000019.10:g.35357169_35357180dup, NC_000019.10:g.35357162_35357180dup, NC_000019.10:g.35357159_35357180dup, NC_000019.10:g.35357158_35357180dup, NC_000019.10:g.35357180_35357181insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.10:g.35357180_35357181insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.35848068_35848082del, NC_000019.9:g.35848070_35848082del, NC_000019.9:g.35848071_35848082del, NC_000019.9:g.35848072_35848082del, NC_000019.9:g.35848073_35848082del, NC_000019.9:g.35848074_35848082del, NC_000019.9:g.35848075_35848082del, NC_000019.9:g.35848076_35848082del, NC_000019.9:g.35848077_35848082del, NC_000019.9:g.35848078_35848082del, NC_000019.9:g.35848079_35848082del, NC_000019.9:g.35848080_35848082del, NC_000019.9:g.35848081_35848082del, NC_000019.9:g.35848082del, NC_000019.9:g.35848082dup, NC_000019.9:g.35848081_35848082dup, NC_000019.9:g.35848080_35848082dup, NC_000019.9:g.35848079_35848082dup, NC_000019.9:g.35848078_35848082dup, NC_000019.9:g.35848077_35848082dup, NC_000019.9:g.35848076_35848082dup, NC_000019.9:g.35848075_35848082dup, NC_000019.9:g.35848074_35848082dup, NC_000019.9:g.35848073_35848082dup, NC_000019.9:g.35848071_35848082dup, NC_000019.9:g.35848064_35848082dup, NC_000019.9:g.35848061_35848082dup, NC_000019.9:g.35848060_35848082dup, NC_000019.9:g.35848082_35848083insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.35848082_35848083insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 148674150517.

rs1486741505 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:35357465 (GRCh38)
19:35848367 (GRCh37)
Canonical SPDI:: NC_000019.10:35357464:T:G
Gene:: FFAR3 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000019.10:g.35357465T>G, NC_000019.9:g.35848367T>G

Select item 148641249018.

rs1486412490 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:35358862 (GRCh38)
19:35849764 (GRCh37)
Canonical SPDI:: NC_000019.10:35358861:G:A
Gene:: FFAR3 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000019.10:g.35358862G>A, NC_000019.9:g.35849764G>A

Select item 148527800219.

rs1485278002 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 19:35360927 (GRCh38)
19:35851829 (GRCh37)
Canonical SPDI:: NC_000019.10:35360926:A:G,NC_000019.10:35360926:A:T
Gene:: FFAR3 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0.000037/1 (TOMMO)
G=0.000042/11 (TOPMED)
G=0.000045/6 (GnomAD)
HGVS:: NC_000019.10:g.35360927A>G, NC_000019.10:g.35360927A>T, NC_000019.9:g.35851829A>G, NC_000019.9:g.35851829A>T

Select item 148497459520.

rs1484974595 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:35359731 (GRCh38)
19:35850633 (GRCh37)
Canonical SPDI:: NC_000019.10:35359730:T:A
Gene:: FFAR3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.0002/1 (ALFA)
HGVS:: NC_000019.10:g.35359731T>A, NC_000019.9:g.35850633T>A, NM_005304.5:c.841T>A, NM_005304.4:c.841T>A, NM_005304.3:c.841T>A, XM_011526858.3:c.952T>A, XM_011526858.2:c.952T>A, XM_011526858.1:c.952T>A, NP_005295.1:p.Ser281Thr, XP_011525160.1:p.Ser318Thr

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