SNP Links for Nucleotide (Select 229892268) - SNP

Links from Nucleotide

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Select item 14915676001.

rs1491567600 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 13:28301171 (GRCh38)
13:28875309 (GRCh37)
Canonical SPDI:: NC_000013.11:28301171::A
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0.00007/1 (ALFA)
HGVS:: NC_000013.11:g.28301171_28301172insA, NC_000013.10:g.28875308_28875309insA, NG_012003.1:g.198957_198958insT, NM_002019.4:c.*1995_*1996insT, XM_017020485.1:c.*1995_*1996insT

Select item 14914284572.

rs1491428457 [Homo sapiens]

Variant type:: SNV:
Alleles:: GG>-
Chromosome:: no mapping
Canonical SPDI:

Select item 14913576473.

rs1491357647 [Homo sapiens]

Variant type:: DELINS
Alleles:: CC>- [Show Flanks]
Chromosome:: 13:28300521 (GRCh38)
13:28874658 (GRCh37)
Canonical SPDI:: NC_000013.11:28300519:CCC:C
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.00034/4 (ALFA)
-=0.00328/21 (1000Genomes)
-=0.00656/308 (GnomAD)
HGVS:: NC_000013.11:g.28300521_28300522del, NC_000013.10:g.28874658_28874659del, NG_012003.1:g.199608_199609del, NM_002019.4:c.*2646_*2647del, XM_017020485.1:c.*2646_*2647del

Select item 14912117604.

rs1491211760 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 13:28300520 (GRCh38)
13:28874658 (GRCh37)
Canonical SPDI:: NC_000013.11:28300520::A
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by cluster
MAF:: A=0.00296/142 (GnomAD)
HGVS:: NC_000013.11:g.28300520_28300521insA, NC_000013.10:g.28874657_28874658insA, NG_012003.1:g.199608_199609insT, NM_002019.4:c.*2646_*2647insT, XM_017020485.1:c.*2646_*2647insT

Select item 14910401275.

rs1491040127 has merged into rs57419092 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACACACACACACACACACA>-,CA,CACA,CACACA,CACACACA,CACACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACACA,CACACACACACACACACACACACA,CACACACACACACACACACACACACA,CACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACACACA [Show Flanks]
Chromosome:: 13:28300538 (GRCh38)
13:28874675 (GRCh37)
Canonical SPDI:: NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000013.11:28300521:CACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACACACACACA
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACACACA=0./0 (ALFA)
HGVS:: NC_000013.11:g.28300522CA[8], NC_000013.11:g.28300522CA[9], NC_000013.11:g.28300522CA[10], NC_000013.11:g.28300522CA[11], NC_000013.11:g.28300522CA[12], NC_000013.11:g.28300522CA[13], NC_000013.11:g.28300522CA[14], NC_000013.11:g.28300522CA[15], NC_000013.11:g.28300522CA[16], NC_000013.11:g.28300522CA[17], NC_000013.11:g.28300522CA[19], NC_000013.11:g.28300522CA[20], NC_000013.11:g.28300522CA[21], NC_000013.11:g.28300522CA[22], NC_000013.11:g.28300522CA[23], NC_000013.11:g.28300522CA[24], NC_000013.11:g.28300522CA[25], NC_000013.11:g.28300522CA[27], NC_000013.11:g.28300522CA[28], NC_000013.10:g.28874659CA[8], NC_000013.10:g.28874659CA[9], NC_000013.10:g.28874659CA[10], NC_000013.10:g.28874659CA[11], NC_000013.10:g.28874659CA[12], NC_000013.10:g.28874659CA[13], NC_000013.10:g.28874659CA[14], NC_000013.10:g.28874659CA[15], NC_000013.10:g.28874659CA[16], NC_000013.10:g.28874659CA[17], NC_000013.10:g.28874659CA[19], NC_000013.10:g.28874659CA[20], NC_000013.10:g.28874659CA[21], NC_000013.10:g.28874659CA[22], NC_000013.10:g.28874659CA[23], NC_000013.10:g.28874659CA[24], NC_000013.10:g.28874659CA[25], NC_000013.10:g.28874659CA[27], NC_000013.10:g.28874659CA[28], NG_012003.1:g.199572TG[8], NG_012003.1:g.199572TG[9], NG_012003.1:g.199572TG[10], NG_012003.1:g.199572TG[11], NG_012003.1:g.199572TG[12], NG_012003.1:g.199572TG[13], NG_012003.1:g.199572TG[14], NG_012003.1:g.199572TG[15], NG_012003.1:g.199572TG[16], NG_012003.1:g.199572TG[17], NG_012003.1:g.199572TG[19], NG_012003.1:g.199572TG[20], NG_012003.1:g.199572TG[21], NG_012003.1:g.199572TG[22], NG_012003.1:g.199572TG[23], NG_012003.1:g.199572TG[24], NG_012003.1:g.199572TG[25], NG_012003.1:g.199572TG[27], NG_012003.1:g.199572TG[28], NM_002019.4:c.*2610TG[8], NM_002019.4:c.*2610TG[9], NM_002019.4:c.*2610TG[10], NM_002019.4:c.*2610TG[11], NM_002019.4:c.*2610TG[12], NM_002019.4:c.*2610TG[13], NM_002019.4:c.*2610TG[14], NM_002019.4:c.*2610TG[15], NM_002019.4:c.*2610TG[16], NM_002019.4:c.*2610TG[17], NM_002019.4:c.*2610TG[19], NM_002019.4:c.*2610TG[20], NM_002019.4:c.*2610TG[21], NM_002019.4:c.*2610TG[22], NM_002019.4:c.*2610TG[23], NM_002019.4:c.*2610TG[24], NM_002019.4:c.*2610TG[25], NM_002019.4:c.*2610TG[27], NM_002019.4:c.*2610TG[28], XM_017020485.1:c.*2610TG[8], XM_017020485.1:c.*2610TG[9], XM_017020485.1:c.*2610TG[10], XM_017020485.1:c.*2610TG[11], XM_017020485.1:c.*2610TG[12], XM_017020485.1:c.*2610TG[13], XM_017020485.1:c.*2610TG[14], XM_017020485.1:c.*2610TG[15], XM_017020485.1:c.*2610TG[16], XM_017020485.1:c.*2610TG[17], XM_017020485.1:c.*2610TG[19], XM_017020485.1:c.*2610TG[20], XM_017020485.1:c.*2610TG[21], XM_017020485.1:c.*2610TG[22], XM_017020485.1:c.*2610TG[23], XM_017020485.1:c.*2610TG[24], XM_017020485.1:c.*2610TG[25], XM_017020485.1:c.*2610TG[27], XM_017020485.1:c.*2610TG[28]

Select item 14908961116.

rs1490896111 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:28329719 (GRCh38)
13:28903856 (GRCh37)
Canonical SPDI:: NC_000013.11:28329718:G:A
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28329719G>A, NC_000013.10:g.28903856G>A, NG_012003.1:g.170410C>T, NM_002019.4:c.2603C>T, NP_002010.2:p.Thr868Met

Select item 14904041817.

rs1490404181 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 13:28339215 (GRCh38)
13:28913352 (GRCh37)
Canonical SPDI:: NC_000013.11:28339214:G:A,NC_000013.11:28339214:G:C,NC_000013.11:28339214:G:T
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (GnomAD)
A=0.00002/5 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28339215G>A, NC_000013.11:g.28339215G>C, NC_000013.11:g.28339215G>T, NC_000013.10:g.28913352G>A, NC_000013.10:g.28913352G>C, NC_000013.10:g.28913352G>T, NG_012003.1:g.160914C>T, NG_012003.1:g.160914C>G, NG_012003.1:g.160914C>A, NM_002019.4:c.2441C>T, NM_002019.4:c.2441C>G, NM_002019.4:c.2441C>A, XM_017020485.1:c.2441C>T, XM_017020485.1:c.2441C>G, XM_017020485.1:c.2441C>A, NP_002010.2:p.Pro814Leu, NP_002010.2:p.Pro814Arg, NP_002010.2:p.Pro814His, XP_016875974.1:p.Pro814Leu, XP_016875974.1:p.Pro814Arg, XP_016875974.1:p.Pro814His

Select item 14902699748.

rs1490269974 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 13:28302141 (GRCh38)
13:28876278 (GRCh37)
Canonical SPDI:: NC_000013.11:28302140:C:G
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by cluster
MAF:: G=0.0005/1 (Korea1K)
HGVS:: NC_000013.11:g.28302141C>G, NC_000013.10:g.28876278C>G, NG_012003.1:g.197988G>C, NM_002019.4:c.*1026G>C, XM_017020485.1:c.*1026G>C

Select item 14898436419.

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 148945260510.

rs1489452605 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 13:28302805 (GRCh38)
13:28876942 (GRCh37)
Canonical SPDI:: NC_000013.11:28302804:G:C
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000015/2 (GnomAD)
HGVS:: NC_000013.11:g.28302805G>C, NC_000013.10:g.28876942G>C, NG_012003.1:g.197324C>G, NM_002019.4:c.*362C>G, XM_017020485.1:c.*362C>G

Select item 148943160911.

rs1489431609 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:28357640 (GRCh38)
13:28931777 (GRCh37)
Canonical SPDI:: NC_000013.11:28357639:A:G
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.28357640A>G, NC_000013.10:g.28931777A>G, NG_012003.1:g.142489T>C, NM_002019.4:c.2162T>C, XM_017020485.1:c.2162T>C, NP_002010.2:p.Val721Ala, XP_016875974.1:p.Val721Ala

Select item 148942035312.

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 148929259613.

rs1489292596 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 13:28300539 (GRCh38)
13:28874676 (GRCh37)
Canonical SPDI:: NC_000013.11:28300538:A:C
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.28300539A>C, NC_000013.10:g.28874676A>C, NG_012003.1:g.199590T>G, NM_002019.4:c.*2628T>G, XM_017020485.1:c.*2628T>G

Select item 148769668414.

rs1487696684 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 13:28301394 (GRCh38)
13:28875531 (GRCh37)
Canonical SPDI:: NC_000013.11:28301393:A:C
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.28301394A>C, NC_000013.10:g.28875531A>C, NG_012003.1:g.198735T>G, NM_002019.4:c.*1773T>G, XM_017020485.1:c.*1773T>G

Select item 148576534515.

rs1485765345 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:28303268 (GRCh38)
13:28877405 (GRCh37)
Canonical SPDI:: NC_000013.11:28303267:T:C
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28303268T>C, NC_000013.10:g.28877405T>C, NG_012003.1:g.196861A>G, NM_002019.4:c.3916A>G, XM_017020485.1:c.3802A>G, NP_002010.2:p.Arg1306Gly, XP_016875974.1:p.Arg1268Gly

Select item 148548897416.

rs1485488974 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 13:28301649 (GRCh38)
13:28875786 (GRCh37)
Canonical SPDI:: NC_000013.11:28301648:A:G,NC_000013.11:28301648:A:T
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.28301649A>G, NC_000013.11:g.28301649A>T, NC_000013.10:g.28875786A>G, NC_000013.10:g.28875786A>T, NG_012003.1:g.198480T>C, NG_012003.1:g.198480T>A, NM_002019.4:c.*1518T>C, NM_002019.4:c.*1518T>A, XM_017020485.1:c.*1518T>C, XM_017020485.1:c.*1518T>A

Select item 148486874817.

rs1484868748 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:28300595 (GRCh38)
13:28874732 (GRCh37)
Canonical SPDI:: NC_000013.11:28300594:C:T
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.28300595C>T, NC_000013.10:g.28874732C>T, NG_012003.1:g.199534G>A, NM_002019.4:c.*2572G>A, XM_017020485.1:c.*2572G>A

Select item 148456291718.

rs1484562917 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 13:28301379 (GRCh38)
13:28875516 (GRCh37)
Canonical SPDI:: NC_000013.11:28301378:C:G,NC_000013.11:28301378:C:T
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.28301379C>G, NC_000013.11:g.28301379C>T, NC_000013.10:g.28875516C>G, NC_000013.10:g.28875516C>T, NG_012003.1:g.198750G>C, NG_012003.1:g.198750G>A, NM_002019.4:c.*1788G>C, NM_002019.4:c.*1788G>A, XM_017020485.1:c.*1788G>C, XM_017020485.1:c.*1788G>A

Select item 148442141519.

rs1484421415 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:28303204 (GRCh38)
13:28877341 (GRCh37)
Canonical SPDI:: NC_000013.11:28303203:T:C
Gene:: FLT1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.28303204T>C, NC_000013.10:g.28877341T>C, NG_012003.1:g.196925A>G, NM_002019.4:c.3980A>G, XM_017020485.1:c.3866A>G, NP_002010.2:p.Tyr1327Cys, XP_016875974.1:p.Tyr1289Cys

Select item 148229072120.

rs1482290721 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:28494890 (GRCh38)
13:29069027 (GRCh37)
Canonical SPDI:: NC_000013.11:28494889:G:A
Gene:: FLT1 (Varview)
Functional Consequence:: 5_prime_UTR_variant
HGVS:: NC_000013.11:g.28494890G>A, NC_000013.10:g.29069027G>A, NG_012003.1:g.5239C>T, NM_002019.4:c.-47C>T, NM_001159920.2:c.-47C>T, NM_001159920.1:c.-47C>T, NM_001160030.2:c.-47C>T, NM_001160030.1:c.-47C>T, NM_001160031.1:c.-47C>T, XM_011535014.2:c.-47C>T, XM_011535014.1:c.-47C>T, XM_017020485.1:c.-47C>T

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