SNP Links for Protein (Select 229892220) - SNP

Select item 14898436411.

rs1489843641 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:28390024 (GRCh38)
13:28964161 (GRCh37)
Canonical SPDI:: NC_000013.11:28390023:T:C
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28390024T>C, NC_000013.10:g.28964161T>C, NG_012003.1:g.110105A>G, NM_002019.4:c.1741A>G, NM_001159920.2:c.1741A>G, NM_001159920.1:c.1741A>G, NM_001160030.2:c.1741A>G, NM_001160030.1:c.1741A>G, XM_011535014.2:c.1741A>G, XM_011535014.1:c.1741A>G, XM_017020485.1:c.1741A>G, NP_002010.2:p.Lys581Glu, NP_001153392.1:p.Lys581Glu, NP_001153502.1:p.Lys581Glu, XP_011533316.1:p.Lys581Glu, XP_016875974.1:p.Lys581Glu

Select item 14894203532.

rs1489420353 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:28390098 (GRCh38)
13:28964235 (GRCh37)
Canonical SPDI:: NC_000013.11:28390097:G:A
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28390098G>A, NC_000013.10:g.28964235G>A, NG_012003.1:g.110031C>T, NM_002019.4:c.1667C>T, NM_001159920.2:c.1667C>T, NM_001159920.1:c.1667C>T, NM_001160030.2:c.1667C>T, NM_001160030.1:c.1667C>T, XM_011535014.2:c.1667C>T, XM_011535014.1:c.1667C>T, XM_017020485.1:c.1667C>T, NP_002010.2:p.Pro556Leu, NP_001153392.1:p.Pro556Leu, NP_001153502.1:p.Pro556Leu, XP_011533316.1:p.Pro556Leu, XP_016875974.1:p.Pro556Leu

Select item 14817539023.

rs1481753902 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 13:28405838 (GRCh38)
13:28979975 (GRCh37)
Canonical SPDI:: NC_000013.11:28405837:A:G,NC_000013.11:28405837:A:T
Gene:: FLT1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28405838A>G, NC_000013.11:g.28405838A>T, NC_000013.10:g.28979975A>G, NC_000013.10:g.28979975A>T, NG_012003.1:g.94291T>C, NG_012003.1:g.94291T>A, NM_002019.4:c.1493T>C, NM_002019.4:c.1493T>A, NM_001159920.2:c.1493T>C, NM_001159920.2:c.1493T>A, NM_001159920.1:c.1493T>C, NM_001159920.1:c.1493T>A, NM_001160030.2:c.1493T>C, NM_001160030.2:c.1493T>A, NM_001160030.1:c.1493T>C, NM_001160030.1:c.1493T>A, NM_001160031.1:c.1493T>C, NM_001160031.1:c.1493T>A, XM_011535014.2:c.1493T>C, XM_011535014.2:c.1493T>A, XM_011535014.1:c.1493T>C, XM_011535014.1:c.1493T>A, XM_017020485.1:c.1493T>C, XM_017020485.1:c.1493T>A, NP_002010.2:p.Met498Thr, NP_002010.2:p.Met498Lys, NP_001153392.1:p.Met498Thr, NP_001153392.1:p.Met498Lys, NP_001153502.1:p.Met498Thr, NP_001153502.1:p.Met498Lys, NP_001153503.1:p.Met498Thr, NP_001153503.1:p.Met498Lys, XP_011533316.1:p.Met498Thr, XP_011533316.1:p.Met498Lys, XP_016875974.1:p.Met498Thr, XP_016875974.1:p.Met498Lys

Select item 14798264264.

rs1479826426 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 13:28389933 (GRCh38)
13:28964070 (GRCh37)
Canonical SPDI:: NC_000013.11:28389932:A:T
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
HGVS:: NC_000013.11:g.28389933A>T, NC_000013.10:g.28964070A>T, NG_012003.1:g.110196T>A, NM_002019.4:c.1832T>A, NM_001159920.2:c.1832T>A, NM_001159920.1:c.1832T>A, NM_001160030.2:c.1832T>A, NM_001160030.1:c.1832T>A, XM_011535014.2:c.1832T>A, XM_011535014.1:c.1832T>A, XM_017020485.1:c.1832T>A, NP_002010.2:p.Ile611Asn, NP_001153392.1:p.Ile611Asn, NP_001153502.1:p.Ile611Asn, XP_011533316.1:p.Ile611Asn, XP_016875974.1:p.Ile611Asn

Select item 14777658175.

rs1477765817 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 13:28397061 (GRCh38)
13:28971198 (GRCh37)
Canonical SPDI:: NC_000013.11:28397060:C:G
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28397061C>G, NC_000013.10:g.28971198C>G, NG_012003.1:g.103068G>C, NM_002019.4:c.1559G>C, NM_001159920.2:c.1559G>C, NM_001159920.1:c.1559G>C, NM_001160030.2:c.1559G>C, NM_001160030.1:c.1559G>C, XM_011535014.2:c.1559G>C, XM_011535014.1:c.1559G>C, XM_017020485.1:c.1559G>C, NP_002010.2:p.Ser520Thr, NP_001153392.1:p.Ser520Thr, NP_001153502.1:p.Ser520Thr, XP_011533316.1:p.Ser520Thr, XP_016875974.1:p.Ser520Thr

Select item 14759170296.

rs1475917029 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:28438259 (GRCh38)
13:29012396 (GRCh37)
Canonical SPDI:: NC_000013.11:28438258:G:A
Gene:: FLT1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.28438259G>A, NC_000013.10:g.29012396G>A, NG_012003.1:g.61870C>T, NM_002019.4:c.475C>T, NM_001159920.2:c.475C>T, NM_001159920.1:c.475C>T, NM_001160030.2:c.475C>T, NM_001160030.1:c.475C>T, NM_001160031.1:c.475C>T, XM_011535014.2:c.475C>T, XM_011535014.1:c.475C>T, XM_017020485.1:c.475C>T, NP_002010.2:p.Arg159Trp, NP_001153392.1:p.Arg159Trp, NP_001153502.1:p.Arg159Trp, NP_001153503.1:p.Arg159Trp, XP_011533316.1:p.Arg159Trp, XP_016875974.1:p.Arg159Trp

Select item 14735009147.

rs1473500914 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 13:28434118 (GRCh38)
13:29008255 (GRCh37)
Canonical SPDI:: NC_000013.11:28434117:T:A
Gene:: FLT1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000111/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28434118T>A, NC_000013.10:g.29008255T>A, NG_012003.1:g.66011A>T, NM_002019.4:c.616A>T, NM_001159920.2:c.616A>T, NM_001159920.1:c.616A>T, NM_001160030.2:c.616A>T, NM_001160030.1:c.616A>T, NM_001160031.1:c.616A>T, XM_011535014.2:c.616A>T, XM_011535014.1:c.616A>T, XM_017020485.1:c.616A>T, NP_002010.2:p.Thr206Ser, NP_001153392.1:p.Thr206Ser, NP_001153502.1:p.Thr206Ser, NP_001153503.1:p.Thr206Ser, XP_011533316.1:p.Thr206Ser, XP_016875974.1:p.Thr206Ser

Select item 14733094048.

rs1473309404 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:28427301 (GRCh38)
13:29001438 (GRCh37)
Canonical SPDI:: NC_000013.11:28427300:C:T
Gene:: FLT1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.28427301C>T, NC_000013.10:g.29001438C>T, NG_012003.1:g.72828G>A, NM_002019.4:c.1294G>A, NM_001159920.2:c.1294G>A, NM_001159920.1:c.1294G>A, NM_001160030.2:c.1294G>A, NM_001160030.1:c.1294G>A, NM_001160031.1:c.1294G>A, XM_011535014.2:c.1294G>A, XM_011535014.1:c.1294G>A, XM_017020485.1:c.1294G>A, NP_002010.2:p.Glu432Lys, NP_001153392.1:p.Glu432Lys, NP_001153502.1:p.Glu432Lys, NP_001153503.1:p.Glu432Lys, XP_011533316.1:p.Glu432Lys, XP_016875974.1:p.Glu432Lys

Select item 14732584469.

rs1473258446 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:28467059 (GRCh38)
13:29041196 (GRCh37)
Canonical SPDI:: NC_000013.11:28467058:T:C
Gene:: FLT1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28467059T>C, NC_000013.10:g.29041196T>C, NG_012003.1:g.33070A>G, NM_002019.4:c.232A>G, NM_001159920.2:c.232A>G, NM_001159920.1:c.232A>G, NM_001160030.2:c.232A>G, NM_001160030.1:c.232A>G, NM_001160031.1:c.232A>G, XM_011535014.2:c.232A>G, XM_011535014.1:c.232A>G, XM_017020485.1:c.232A>G, NP_002010.2:p.Lys78Glu, NP_001153392.1:p.Lys78Glu, NP_001153502.1:p.Lys78Glu, NP_001153503.1:p.Lys78Glu, XP_011533316.1:p.Lys78Glu, XP_016875974.1:p.Lys78Glu

Select item 147310256710.

rs1473102567 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 13:28405799 (GRCh38)
13:28979936 (GRCh37)
Canonical SPDI:: NC_000013.11:28405798:A:C,NC_000013.11:28405798:A:T
Gene:: FLT1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000047/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28405799A>C, NC_000013.11:g.28405799A>T, NC_000013.10:g.28979936A>C, NC_000013.10:g.28979936A>T, NG_012003.1:g.94330T>G, NG_012003.1:g.94330T>A, NM_002019.4:c.1532T>G, NM_002019.4:c.1532T>A, NM_001159920.2:c.1532T>G, NM_001159920.2:c.1532T>A, NM_001159920.1:c.1532T>G, NM_001159920.1:c.1532T>A, NM_001160030.2:c.1532T>G, NM_001160030.2:c.1532T>A, NM_001160030.1:c.1532T>G, NM_001160030.1:c.1532T>A, NM_001160031.1:c.1532T>G, NM_001160031.1:c.1532T>A, XM_011535014.2:c.1532T>G, XM_011535014.2:c.1532T>A, XM_011535014.1:c.1532T>G, XM_011535014.1:c.1532T>A, XM_017020485.1:c.1532T>G, XM_017020485.1:c.1532T>A, NP_002010.2:p.Ile511Arg, NP_002010.2:p.Ile511Lys, NP_001153392.1:p.Ile511Arg, NP_001153392.1:p.Ile511Lys, NP_001153502.1:p.Ile511Arg, NP_001153502.1:p.Ile511Lys, NP_001153503.1:p.Ile511Arg, NP_001153503.1:p.Ile511Lys, XP_011533316.1:p.Ile511Arg, XP_011533316.1:p.Ile511Lys, XP_016875974.1:p.Ile511Arg, XP_016875974.1:p.Ile511Lys

Select item 147018686311.

rs1470186863 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 13:28405878 (GRCh38)
13:28980015 (GRCh37)
Canonical SPDI:: NC_000013.11:28405877:T:G
Gene:: FLT1 (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=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.28405878T>G, NC_000013.10:g.28980015T>G, NG_012003.1:g.94251A>C, NM_002019.4:c.1453A>C, NM_001159920.2:c.1453A>C, NM_001159920.1:c.1453A>C, NM_001160030.2:c.1453A>C, NM_001160030.1:c.1453A>C, NM_001160031.1:c.1453A>C, XM_011535014.2:c.1453A>C, XM_011535014.1:c.1453A>C, XM_017020485.1:c.1453A>C, NP_002010.2:p.Asn485His, NP_001153392.1:p.Asn485His, NP_001153502.1:p.Asn485His, NP_001153503.1:p.Asn485His, XP_011533316.1:p.Asn485His, XP_016875974.1:p.Asn485His

Select item 146945646212.

rs1469456462 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 13:28427262 (GRCh38)
13:29001399 (GRCh37)
Canonical SPDI:: NC_000013.11:28427261:G:C
Gene:: FLT1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28427262G>C, NC_000013.10:g.29001399G>C, NG_012003.1:g.72867C>G, NM_002019.4:c.1333C>G, NM_001159920.2:c.1333C>G, NM_001159920.1:c.1333C>G, NM_001160030.2:c.1333C>G, NM_001160030.1:c.1333C>G, NM_001160031.1:c.1333C>G, XM_011535014.2:c.1333C>G, XM_011535014.1:c.1333C>G, XM_017020485.1:c.1333C>G, NP_002010.2:p.Pro445Ala, NP_001153392.1:p.Pro445Ala, NP_001153502.1:p.Pro445Ala, NP_001153503.1:p.Pro445Ala, XP_011533316.1:p.Pro445Ala, XP_016875974.1:p.Pro445Ala

Select item 146851686113.

rs1468516861 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 13:28467052 (GRCh38)
13:29041189 (GRCh37)
Canonical SPDI:: NC_000013.11:28467051:G:A,NC_000013.11:28467051:G:T
Gene:: FLT1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28467052G>A, NC_000013.11:g.28467052G>T, NC_000013.10:g.29041189G>A, NC_000013.10:g.29041189G>T, NG_012003.1:g.33077C>T, NG_012003.1:g.33077C>A, NM_002019.4:c.239C>T, NM_002019.4:c.239C>A, NM_001159920.2:c.239C>T, NM_001159920.2:c.239C>A, NM_001159920.1:c.239C>T, NM_001159920.1:c.239C>A, NM_001160030.2:c.239C>T, NM_001160030.2:c.239C>A, NM_001160030.1:c.239C>T, NM_001160030.1:c.239C>A, NM_001160031.1:c.239C>T, NM_001160031.1:c.239C>A, XM_011535014.2:c.239C>T, XM_011535014.2:c.239C>A, XM_011535014.1:c.239C>T, XM_011535014.1:c.239C>A, XM_017020485.1:c.239C>T, XM_017020485.1:c.239C>A, NP_002010.2:p.Ala80Val, NP_002010.2:p.Ala80Asp, NP_001153392.1:p.Ala80Val, NP_001153392.1:p.Ala80Asp, NP_001153502.1:p.Ala80Val, NP_001153502.1:p.Ala80Asp, NP_001153503.1:p.Ala80Val, NP_001153503.1:p.Ala80Asp, XP_011533316.1:p.Ala80Val, XP_011533316.1:p.Ala80Asp, XP_016875974.1:p.Ala80Val, XP_016875974.1:p.Ala80Asp

Select item 146782369414.

rs1467823694 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:28389844 (GRCh38)
13:28963981 (GRCh37)
Canonical SPDI:: NC_000013.11:28389843:C:T
Gene:: FLT1 (Varview)
Functional Consequence:: missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28389844C>T, NC_000013.10:g.28963981C>T, NG_012003.1:g.110285G>A, NM_002019.4:c.1921G>A, NM_001159920.2:c.1921G>A, NM_001159920.1:c.1921G>A, NM_001160030.2:c.1921G>A, NM_001160030.1:c.1921G>A, XM_011535014.2:c.1921G>A, XM_011535014.1:c.1921G>A, XM_017020485.1:c.1921G>A, NP_002010.2:p.Val641Ile, NP_001153392.1:p.Val641Ile, NP_001153502.1:p.Val641Ile, XP_011533316.1:p.Val641Ile, XP_016875974.1:p.Val641Ile

Select item 146665786615.

rs1466657866 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:28431137 (GRCh38)
13:29005274 (GRCh37)
Canonical SPDI:: NC_000013.11:28431136:A:G
Gene:: FLT1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.28431137A>G, NC_000013.10:g.29005274A>G, NG_012003.1:g.68992T>C, NM_002019.4:c.987T>C, NM_001159920.2:c.987T>C, NM_001159920.1:c.987T>C, NM_001160030.2:c.987T>C, NM_001160030.1:c.987T>C, NM_001160031.1:c.987T>C, XM_011535014.2:c.987T>C, XM_011535014.1:c.987T>C, XM_017020485.1:c.987T>C

Select item 146549828216.

rs1465498282 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 13:28466933 (GRCh38)
13:29041070 (GRCh37)
Canonical SPDI:: NC_000013.11:28466932:T:G
Gene:: FLT1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28466933T>G, NC_000013.10:g.29041070T>G, NG_012003.1:g.33196A>C, NM_002019.4:c.358A>C, NM_001159920.2:c.358A>C, NM_001159920.1:c.358A>C, NM_001160030.2:c.358A>C, NM_001160030.1:c.358A>C, NM_001160031.1:c.358A>C, XM_011535014.2:c.358A>C, XM_011535014.1:c.358A>C, XM_017020485.1:c.358A>C, NP_002010.2:p.Thr120Pro, NP_001153392.1:p.Thr120Pro, NP_001153502.1:p.Thr120Pro, NP_001153503.1:p.Thr120Pro, XP_011533316.1:p.Thr120Pro, XP_016875974.1:p.Thr120Pro

Select item 146461946317.

rs1464619463 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 13:28430109 (GRCh38)
13:29004246 (GRCh37)
Canonical SPDI:: NC_000013.11:28430108:G:T
Gene:: FLT1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0.0001/1 (ALFA)
HGVS:: NC_000013.11:g.28430109G>T, NC_000013.10:g.29004246G>T, NG_012003.1:g.70020C>A, NM_002019.4:c.1047C>A, NM_001159920.2:c.1047C>A, NM_001159920.1:c.1047C>A, NM_001160030.2:c.1047C>A, NM_001160030.1:c.1047C>A, NM_001160031.1:c.1047C>A, XM_011535014.2:c.1047C>A, XM_011535014.1:c.1047C>A, XM_017020485.1:c.1047C>A

Select item 146426160618.

rs1464261606 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 13:28405869 (GRCh38)
13:28980006 (GRCh37)
Canonical SPDI:: NC_000013.11:28405868:C:A,NC_000013.11:28405868:C:G,NC_000013.11:28405868:C:T
Gene:: FLT1 (Varview)
Functional Consequence:: stop_gained,missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28405869C>A, NC_000013.11:g.28405869C>G, NC_000013.11:g.28405869C>T, NC_000013.10:g.28980006C>A, NC_000013.10:g.28980006C>G, NC_000013.10:g.28980006C>T, NG_012003.1:g.94260G>T, NG_012003.1:g.94260G>C, NG_012003.1:g.94260G>A, NM_002019.4:c.1462G>T, NM_002019.4:c.1462G>C, NM_002019.4:c.1462G>A, NM_001159920.2:c.1462G>T, NM_001159920.2:c.1462G>C, NM_001159920.2:c.1462G>A, NM_001159920.1:c.1462G>T, NM_001159920.1:c.1462G>C, NM_001159920.1:c.1462G>A, NM_001160030.2:c.1462G>T, NM_001160030.2:c.1462G>C, NM_001160030.2:c.1462G>A, NM_001160030.1:c.1462G>T, NM_001160030.1:c.1462G>C, NM_001160030.1:c.1462G>A, NM_001160031.1:c.1462G>T, NM_001160031.1:c.1462G>C, NM_001160031.1:c.1462G>A, XM_011535014.2:c.1462G>T, XM_011535014.2:c.1462G>C, XM_011535014.2:c.1462G>A, XM_011535014.1:c.1462G>T, XM_011535014.1:c.1462G>C, XM_011535014.1:c.1462G>A, XM_017020485.1:c.1462G>T, XM_017020485.1:c.1462G>C, XM_017020485.1:c.1462G>A, NP_002010.2:p.Glu488Ter, NP_002010.2:p.Glu488Gln, NP_002010.2:p.Glu488Lys, NP_001153392.1:p.Glu488Ter, NP_001153392.1:p.Glu488Gln, NP_001153392.1:p.Glu488Lys, NP_001153502.1:p.Glu488Ter, NP_001153502.1:p.Glu488Gln, NP_001153502.1:p.Glu488Lys, NP_001153503.1:p.Glu488Ter, NP_001153503.1:p.Glu488Gln, NP_001153503.1:p.Glu488Lys, XP_011533316.1:p.Glu488Ter, XP_011533316.1:p.Glu488Gln, XP_011533316.1:p.Glu488Lys, XP_016875974.1:p.Glu488Ter, XP_016875974.1:p.Glu488Gln, XP_016875974.1:p.Glu488Lys

Select item 146414606619.

rs1464146066 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:28467569 (GRCh38)
13:29041706 (GRCh37)
Canonical SPDI:: NC_000013.11:28467568:C:T
Gene:: FLT1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by cluster
HGVS:: NC_000013.11:g.28467569C>T, NC_000013.10:g.29041706C>T, NG_012003.1:g.32560G>A, NM_002019.4:c.113G>A, NM_001159920.2:c.113G>A, NM_001159920.1:c.113G>A, NM_001160030.2:c.113G>A, NM_001160030.1:c.113G>A, NM_001160031.1:c.113G>A, XM_011535014.2:c.113G>A, XM_011535014.1:c.113G>A, XM_017020485.1:c.113G>A, NP_002010.2:p.Gly38Asp, NP_001153392.1:p.Gly38Asp, NP_001153502.1:p.Gly38Asp, NP_001153503.1:p.Gly38Asp, XP_011533316.1:p.Gly38Asp, XP_016875974.1:p.Gly38Asp

Select item 146000354020.

rs1460003540 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:28431241 (GRCh38)
13:29005378 (GRCh37)
Canonical SPDI:: NC_000013.11:28431240:C:T
Gene:: FLT1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
T=0.000546/1 (Korea1K)
HGVS:: NC_000013.11:g.28431241C>T, NC_000013.10:g.29005378C>T, NG_012003.1:g.68888G>A, NM_002019.4:c.883G>A, NM_001159920.2:c.883G>A, NM_001159920.1:c.883G>A, NM_001160030.2:c.883G>A, NM_001160030.1:c.883G>A, NM_001160031.1:c.883G>A, XM_011535014.2:c.883G>A, XM_011535014.1:c.883G>A, XM_017020485.1:c.883G>A, NP_002010.2:p.Val295Ile, NP_001153392.1:p.Val295Ile, NP_001153502.1:p.Val295Ile, NP_001153503.1:p.Val295Ile, XP_011533316.1:p.Val295Ile, XP_016875974.1:p.Val295Ile

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