SNP Links for Nucleotide (Select 398303815) - SNP

Links from Nucleotide

Items: 1 to 20 of 1197

<< First< Prev

Page of 60

Next >Last >>

Select item 14900865741.

rs1490086574 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:31852588 (GRCh38)
10:32141516 (GRCh37)
Canonical SPDI:: NC_000010.11:31852587:G:A
Gene:: ARHGAP12 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.31852588G>A, NC_000010.10:g.32141516G>A, NM_018287.7:c.1099C>T, NM_018287.6:c.1099C>T, XM_005252644.3:c.958C>T, XM_005252644.2:c.958C>T, XM_005252644.1:c.958C>T, NM_001270696.2:c.1099C>T, NM_001270696.1:c.1099C>T, NM_001270698.2:c.958C>T, NM_001270698.1:c.958C>T, NM_001270695.1:c.1099C>T, NM_001270697.1:c.958C>T, NM_001270699.1:c.958C>T, NP_060757.4:p.His367Tyr, XP_005252701.1:p.His320Tyr, NP_001257625.1:p.His367Tyr, NP_001257627.1:p.His320Tyr, NP_001257624.1:p.His367Tyr, NP_001257626.1:p.His320Tyr, NP_001257628.1:p.His320Tyr

Select item 14900301872.

rs1490030187 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:31908275 (GRCh38)
10:32197203 (GRCh37)
Canonical SPDI:: NC_000010.11:31908274:G:A
Gene:: ARHGAP12 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.31908275G>A, NC_000010.10:g.32197203G>A, NM_018287.7:c.581C>T, NM_018287.6:c.581C>T, XM_005252644.3:c.581C>T, XM_005252644.2:c.581C>T, XM_005252644.1:c.581C>T, XM_011519761.3:c.581C>T, XM_011519761.2:c.581C>T, XM_011519761.1:c.581C>T, XM_017016954.3:c.581C>T, XM_017016954.2:c.581C>T, XM_017016954.1:c.581C>T, NM_001270696.2:c.581C>T, NM_001270696.1:c.581C>T, NM_001270698.2:c.581C>T, NM_001270698.1:c.581C>T, NM_001270695.1:c.581C>T, NM_001270697.1:c.581C>T, XM_047426021.1:c.581C>T, NM_001270699.1:c.581C>T, NP_060757.4:p.Ser194Phe, XP_005252701.1:p.Ser194Phe, XP_011518063.1:p.Ser194Phe, XP_016872443.1:p.Ser194Phe, NP_001257625.1:p.Ser194Phe, NP_001257627.1:p.Ser194Phe, NP_001257624.1:p.Ser194Phe, NP_001257626.1:p.Ser194Phe, XP_047281977.1:p.Ser194Phe, NP_001257628.1:p.Ser194Phe

Select item 14890781163.

rs1489078116 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:31805696 (GRCh38)
10:32094624 (GRCh37)
Canonical SPDI:: NC_000010.11:31805695:A:G
Gene:: ARHGAP12 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.31805696A>G, NC_000010.10:g.32094624A>G, NM_018287.7:c.*1962T>C, NM_018287.6:c.*1962T>C, XM_005252644.3:c.*1962T>C, XM_005252644.2:c.*1962T>C, XM_005252644.1:c.*1962T>C, XM_011519761.3:c.*1962T>C, XM_011519761.2:c.*1962T>C, XM_011519761.1:c.*1962T>C, XM_017016954.3:c.*1962T>C, XM_017016954.2:c.*1962T>C, XM_017016954.1:c.*1962T>C, NM_001270696.2:c.*1962T>C, NM_001270696.1:c.*1962T>C, NM_001270698.2:c.*1962T>C, NM_001270698.1:c.*1962T>C, NM_001270695.1:c.*1962T>C, NM_001270697.1:c.*1962T>C, XM_047426021.1:c.*1962T>C, NM_001270699.1:c.*1962T>C

Select item 14871592994.

rs1487159299 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:31820403 (GRCh38)
10:32109331 (GRCh37)
Canonical SPDI:: NC_000010.11:31820402:T:C
Gene:: ARHGAP12 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.31820403T>C, NC_000010.10:g.32109331T>C, NM_018287.7:c.1616A>G, NM_018287.6:c.1616A>G, XM_005252644.3:c.1460A>G, XM_005252644.2:c.1460A>G, XM_005252644.1:c.1460A>G, XM_011519761.3:c.1394A>G, XM_011519761.2:c.1394A>G, XM_011519761.1:c.1394A>G, XM_017016954.3:c.1304A>G, XM_017016954.2:c.1304A>G, XM_017016954.1:c.1304A>G, NM_001270696.2:c.1526A>G, NM_001270696.1:c.1526A>G, NM_001270698.2:c.1385A>G, NM_001270698.1:c.1385A>G, NM_001270695.1:c.1601A>G, NM_001270697.1:c.1475A>G, XM_047426021.1:c.1379A>G, NM_001270699.1:c.1460A>G, NP_060757.4:p.Lys539Arg, XP_005252701.1:p.Lys487Arg, XP_011518063.1:p.Lys465Arg, XP_016872443.1:p.Lys435Arg, NP_001257625.1:p.Lys509Arg, NP_001257627.1:p.Lys462Arg, NP_001257624.1:p.Lys534Arg, NP_001257626.1:p.Lys492Arg, XP_047281977.1:p.Lys460Arg, NP_001257628.1:p.Lys487Arg

Select item 14871063885.

rs1487106388 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:31908196 (GRCh38)
10:32197124 (GRCh37)
Canonical SPDI:: NC_000010.11:31908195:G:A
Gene:: ARHGAP12 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.31908196G>A, NC_000010.10:g.32197124G>A, NM_018287.7:c.660C>T, NM_018287.6:c.660C>T, XM_005252644.3:c.660C>T, XM_005252644.2:c.660C>T, XM_005252644.1:c.660C>T, XM_011519761.3:c.660C>T, XM_011519761.2:c.660C>T, XM_011519761.1:c.660C>T, XM_017016954.3:c.660C>T, XM_017016954.2:c.660C>T, XM_017016954.1:c.660C>T, NM_001270696.2:c.660C>T, NM_001270696.1:c.660C>T, NM_001270698.2:c.660C>T, NM_001270698.1:c.660C>T, NM_001270695.1:c.660C>T, NM_001270697.1:c.660C>T, XM_047426021.1:c.660C>T, NM_001270699.1:c.660C>T

Select item 14856739386.

rs1485673938 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:31908497 (GRCh38)
10:32197425 (GRCh37)
Canonical SPDI:: NC_000010.11:31908496:G:A,NC_000010.11:31908496:G:C
Gene:: ARHGAP12 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000031/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.31908497G>A, NC_000010.11:g.31908497G>C, NC_000010.10:g.32197425G>A, NC_000010.10:g.32197425G>C, NM_018287.7:c.359C>T, NM_018287.7:c.359C>G, NM_018287.6:c.359C>T, NM_018287.6:c.359C>G, XM_005252644.3:c.359C>T, XM_005252644.3:c.359C>G, XM_005252644.2:c.359C>T, XM_005252644.2:c.359C>G, XM_005252644.1:c.359C>T, XM_005252644.1:c.359C>G, XM_011519761.3:c.359C>T, XM_011519761.3:c.359C>G, XM_011519761.2:c.359C>T, XM_011519761.2:c.359C>G, XM_011519761.1:c.359C>T, XM_011519761.1:c.359C>G, XM_017016954.3:c.359C>T, XM_017016954.3:c.359C>G, XM_017016954.2:c.359C>T, XM_017016954.2:c.359C>G, XM_017016954.1:c.359C>T, XM_017016954.1:c.359C>G, NM_001270696.2:c.359C>T, NM_001270696.2:c.359C>G, NM_001270696.1:c.359C>T, NM_001270696.1:c.359C>G, NM_001270698.2:c.359C>T, NM_001270698.2:c.359C>G, NM_001270698.1:c.359C>T, NM_001270698.1:c.359C>G, NM_001270695.1:c.359C>T, NM_001270695.1:c.359C>G, NM_001270697.1:c.359C>T, NM_001270697.1:c.359C>G, XM_047426021.1:c.359C>T, XM_047426021.1:c.359C>G, NM_001270699.1:c.359C>T, NM_001270699.1:c.359C>G, NP_060757.4:p.Ser120Leu, NP_060757.4:p.Ser120Trp, XP_005252701.1:p.Ser120Leu, XP_005252701.1:p.Ser120Trp, XP_011518063.1:p.Ser120Leu, XP_011518063.1:p.Ser120Trp, XP_016872443.1:p.Ser120Leu, XP_016872443.1:p.Ser120Trp, NP_001257625.1:p.Ser120Leu, NP_001257625.1:p.Ser120Trp, NP_001257627.1:p.Ser120Leu, NP_001257627.1:p.Ser120Trp, NP_001257624.1:p.Ser120Leu, NP_001257624.1:p.Ser120Trp, NP_001257626.1:p.Ser120Leu, NP_001257626.1:p.Ser120Trp, XP_047281977.1:p.Ser120Leu, XP_047281977.1:p.Ser120Trp, NP_001257628.1:p.Ser120Leu, NP_001257628.1:p.Ser120Trp

Select item 14854654197.

rs1485465419 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:31806108 (GRCh38)
10:32095036 (GRCh37)
Canonical SPDI:: NC_000010.11:31806107:G:A
Gene:: ARHGAP12 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000015/4 (TOPMED)
A=0.000029/4 (GnomAD)
HGVS:: NC_000010.11:g.31806108G>A, NC_000010.10:g.32095036G>A, NM_018287.7:c.*1550C>T, NM_018287.6:c.*1550C>T, XM_005252644.3:c.*1550C>T, XM_005252644.2:c.*1550C>T, XM_005252644.1:c.*1550C>T, XM_011519761.3:c.*1550C>T, XM_011519761.2:c.*1550C>T, XM_011519761.1:c.*1550C>T, XM_017016954.3:c.*1550C>T, XM_017016954.2:c.*1550C>T, XM_017016954.1:c.*1550C>T, NM_001270696.2:c.*1550C>T, NM_001270696.1:c.*1550C>T, NM_001270698.2:c.*1550C>T, NM_001270698.1:c.*1550C>T, NM_001270695.1:c.*1550C>T, NM_001270697.1:c.*1550C>T, XM_047426021.1:c.*1550C>T, NM_001270699.1:c.*1550C>T

Select item 14853845008.

rs1485384500 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:31861594 (GRCh38)
10:32150522 (GRCh37)
Canonical SPDI:: NC_000010.11:31861593:T:C
Gene:: ARHGAP12 (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=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.31861594T>C, NC_000010.10:g.32150522T>C, NM_018287.7:c.749A>G, NM_018287.6:c.749A>G, XM_005252644.3:c.749A>G, XM_005252644.2:c.749A>G, XM_005252644.1:c.749A>G, XM_011519761.3:c.749A>G, XM_011519761.2:c.749A>G, XM_011519761.1:c.749A>G, XM_017016954.3:c.749A>G, XM_017016954.2:c.749A>G, XM_017016954.1:c.749A>G, NM_001270696.2:c.749A>G, NM_001270696.1:c.749A>G, NM_001270698.2:c.749A>G, NM_001270698.1:c.749A>G, NM_001270695.1:c.749A>G, NM_001270697.1:c.749A>G, XM_047426021.1:c.749A>G, NM_001270699.1:c.749A>G, NP_060757.4:p.Lys250Arg, XP_005252701.1:p.Lys250Arg, XP_011518063.1:p.Lys250Arg, XP_016872443.1:p.Lys250Arg, NP_001257625.1:p.Lys250Arg, NP_001257627.1:p.Lys250Arg, NP_001257624.1:p.Lys250Arg, NP_001257626.1:p.Lys250Arg, XP_047281977.1:p.Lys250Arg, NP_001257628.1:p.Lys250Arg

Select item 14852508679.

rs1485250867 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:31809288 (GRCh38)
10:32098216 (GRCh37)
Canonical SPDI:: NC_000010.11:31809287:T:C
Gene:: ARHGAP12 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (GnomAD_exomes)
C=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.31809288T>C, NC_000010.10:g.32098216T>C, NM_018287.7:c.2070A>G, NM_018287.6:c.2070A>G, XM_005252644.3:c.1914A>G, XM_005252644.2:c.1914A>G, XM_005252644.1:c.1914A>G, XM_011519761.3:c.1848A>G, XM_011519761.2:c.1848A>G, XM_011519761.1:c.1848A>G, XM_017016954.3:c.1758A>G, XM_017016954.2:c.1758A>G, XM_017016954.1:c.1758A>G, NM_001270696.2:c.1980A>G, NM_001270696.1:c.1980A>G, NM_001270698.2:c.1839A>G, NM_001270698.1:c.1839A>G, NM_001270695.1:c.2055A>G, NM_001270697.1:c.1929A>G, XM_047426021.1:c.1833A>G, NM_001270699.1:c.1914A>G, NP_060757.4:p.Ile690Met, XP_005252701.1:p.Ile638Met, XP_011518063.1:p.Ile616Met, XP_016872443.1:p.Ile586Met, NP_001257625.1:p.Ile660Met, NP_001257627.1:p.Ile613Met, NP_001257624.1:p.Ile685Met, NP_001257626.1:p.Ile643Met, XP_047281977.1:p.Ile611Met, NP_001257628.1:p.Ile638Met

Select item 148504926710.

rs1485049267 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:31807074 (GRCh38)
10:32096002 (GRCh37)
Canonical SPDI:: NC_000010.11:31807073:T:C
Gene:: ARHGAP12 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.31807074T>C, NC_000010.10:g.32096002T>C, NM_018287.7:c.*584A>G, NM_018287.6:c.*584A>G, XM_005252644.3:c.*584A>G, XM_005252644.2:c.*584A>G, XM_005252644.1:c.*584A>G, XM_011519761.3:c.*584A>G, XM_011519761.2:c.*584A>G, XM_011519761.1:c.*584A>G, XM_017016954.3:c.*584A>G, XM_017016954.2:c.*584A>G, XM_017016954.1:c.*584A>G, NM_001270696.2:c.*584A>G, NM_001270696.1:c.*584A>G, NM_001270698.2:c.*584A>G, NM_001270698.1:c.*584A>G, NM_001270695.1:c.*584A>G, NM_001270697.1:c.*584A>G, XM_047426021.1:c.*584A>G, NM_001270699.1:c.*584A>G

Select item 148499771111.

rs1484997711 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:31805816 (GRCh38)
10:32094744 (GRCh37)
Canonical SPDI:: NC_000010.11:31805815:A:G
Gene:: ARHGAP12 (Varview)
Functional Consequence:: 3_prime_UTR_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_000010.11:g.31805816A>G, NC_000010.10:g.32094744A>G, NM_018287.7:c.*1842T>C, NM_018287.6:c.*1842T>C, XM_005252644.3:c.*1842T>C, XM_005252644.2:c.*1842T>C, XM_005252644.1:c.*1842T>C, XM_011519761.3:c.*1842T>C, XM_011519761.2:c.*1842T>C, XM_011519761.1:c.*1842T>C, XM_017016954.3:c.*1842T>C, XM_017016954.2:c.*1842T>C, XM_017016954.1:c.*1842T>C, NM_001270696.2:c.*1842T>C, NM_001270696.1:c.*1842T>C, NM_001270698.2:c.*1842T>C, NM_001270698.1:c.*1842T>C, NM_001270695.1:c.*1842T>C, NM_001270697.1:c.*1842T>C, XM_047426021.1:c.*1842T>C, NM_001270699.1:c.*1842T>C

Select item 148406208612.

rs1484062086 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:31861488 (GRCh38)
10:32150416 (GRCh37)
Canonical SPDI:: NC_000010.11:31861487:G:C
Gene:: ARHGAP12 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000010.11:g.31861488G>C, NC_000010.10:g.32150416G>C, NM_018287.7:c.855C>G, NM_018287.6:c.855C>G, XM_005252644.3:c.855C>G, XM_005252644.2:c.855C>G, XM_005252644.1:c.855C>G, XM_011519761.3:c.855C>G, XM_011519761.2:c.855C>G, XM_011519761.1:c.855C>G, XM_017016954.3:c.855C>G, XM_017016954.2:c.855C>G, XM_017016954.1:c.855C>G, NM_001270696.2:c.855C>G, NM_001270696.1:c.855C>G, NM_001270698.2:c.855C>G, NM_001270698.1:c.855C>G, NM_001270695.1:c.855C>G, NM_001270697.1:c.855C>G, XM_047426021.1:c.855C>G, NM_001270699.1:c.855C>G, NP_060757.4:p.Asn285Lys, XP_005252701.1:p.Asn285Lys, XP_011518063.1:p.Asn285Lys, XP_016872443.1:p.Asn285Lys, NP_001257625.1:p.Asn285Lys, NP_001257627.1:p.Asn285Lys, NP_001257624.1:p.Asn285Lys, NP_001257626.1:p.Asn285Lys, XP_047281977.1:p.Asn285Lys, NP_001257628.1:p.Asn285Lys

Select item 148323995313.

rs1483239953 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:31839644 (GRCh38)
10:32128572 (GRCh37)
Canonical SPDI:: NC_000010.11:31839643:T:C
Gene:: ARHGAP12 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.31839644T>C, NC_000010.10:g.32128572T>C, NM_018287.7:c.1364A>G, NM_018287.6:c.1364A>G, XM_005252644.3:c.1223A>G, XM_005252644.2:c.1223A>G, XM_005252644.1:c.1223A>G, XM_011519761.3:c.1142A>G, XM_011519761.2:c.1142A>G, XM_011519761.1:c.1142A>G, NM_001270695.1:c.1364A>G, NM_001270697.1:c.1223A>G, XM_047426021.1:c.1142A>G, NM_001270699.1:c.1223A>G, NP_060757.4:p.Gln455Arg, XP_005252701.1:p.Gln408Arg, XP_011518063.1:p.Gln381Arg, NP_001257624.1:p.Gln455Arg, NP_001257626.1:p.Gln408Arg, XP_047281977.1:p.Gln381Arg, NP_001257628.1:p.Gln408Arg

Select item 148322971614.

rs1483229716 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 10:31806067 (GRCh38)
10:32094995 (GRCh37)
Canonical SPDI:: NC_000010.11:31806066:A:T
Gene:: ARHGAP12 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.31806067A>T, NC_000010.10:g.32094995A>T, NM_018287.7:c.*1591T>A, NM_018287.6:c.*1591T>A, XM_005252644.3:c.*1591T>A, XM_005252644.2:c.*1591T>A, XM_005252644.1:c.*1591T>A, XM_011519761.3:c.*1591T>A, XM_011519761.2:c.*1591T>A, XM_011519761.1:c.*1591T>A, XM_017016954.3:c.*1591T>A, XM_017016954.2:c.*1591T>A, XM_017016954.1:c.*1591T>A, NM_001270696.2:c.*1591T>A, NM_001270696.1:c.*1591T>A, NM_001270698.2:c.*1591T>A, NM_001270698.1:c.*1591T>A, NM_001270695.1:c.*1591T>A, NM_001270697.1:c.*1591T>A, XM_047426021.1:c.*1591T>A, NM_001270699.1:c.*1591T>A

Select item 148290070115.

rs1482900701 has merged into rs3028478 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACACACACACACACACACACACAC>-,AC,ACAC,ACACAC,ACACACAC,ACACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACAC [Show Flanks]
Chromosome:: 10:31805662 (GRCh38)
10:32094590 (GRCh37)
Canonical SPDI:: NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:31805648:CACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC
Gene:: ARHGAP12 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACACAC=0./0 (ALFA)
-=0.3293/1649 (1000Genomes)
HGVS:: NC_000010.11:g.31805650AC[6], NC_000010.11:g.31805650AC[7], NC_000010.11:g.31805650AC[8], NC_000010.11:g.31805650AC[9], NC_000010.11:g.31805650AC[10], NC_000010.11:g.31805650AC[11], NC_000010.11:g.31805650AC[12], NC_000010.11:g.31805650AC[13], NC_000010.11:g.31805650AC[14], NC_000010.11:g.31805650AC[15], NC_000010.11:g.31805650AC[16], NC_000010.11:g.31805650AC[17], NC_000010.11:g.31805650AC[19], NC_000010.11:g.31805650AC[20], NC_000010.11:g.31805650AC[21], NC_000010.11:g.31805650AC[22], NC_000010.11:g.31805650AC[23], NC_000010.11:g.31805650AC[24], NC_000010.11:g.31805650AC[25], NC_000010.11:g.31805650AC[26], NC_000010.11:g.31805650AC[27], NC_000010.11:g.31805650AC[28], NC_000010.11:g.31805650AC[29], NC_000010.10:g.32094578AC[6], NC_000010.10:g.32094578AC[7], NC_000010.10:g.32094578AC[8], NC_000010.10:g.32094578AC[9], NC_000010.10:g.32094578AC[10], NC_000010.10:g.32094578AC[11], NC_000010.10:g.32094578AC[12], NC_000010.10:g.32094578AC[13], NC_000010.10:g.32094578AC[14], NC_000010.10:g.32094578AC[15], NC_000010.10:g.32094578AC[16], NC_000010.10:g.32094578AC[17], NC_000010.10:g.32094578AC[19], NC_000010.10:g.32094578AC[20], NC_000010.10:g.32094578AC[21], NC_000010.10:g.32094578AC[22], NC_000010.10:g.32094578AC[23], NC_000010.10:g.32094578AC[24], NC_000010.10:g.32094578AC[25], NC_000010.10:g.32094578AC[26], NC_000010.10:g.32094578AC[27], NC_000010.10:g.32094578AC[28], NC_000010.10:g.32094578AC[29], NM_018287.7:c.*1974TG[6], NM_018287.7:c.*1974TG[7], NM_018287.7:c.*1974TG[8], NM_018287.7:c.*1974TG[9], NM_018287.7:c.*1974TG[10], NM_018287.7:c.*1974TG[11], NM_018287.7:c.*1974TG[12], NM_018287.7:c.*1974TG[13], NM_018287.7:c.*1974TG[14], NM_018287.7:c.*1974TG[15], NM_018287.7:c.*1974TG[16], NM_018287.7:c.*1974TG[17], NM_018287.7:c.*1974TG[19], NM_018287.7:c.*1974TG[20], NM_018287.7:c.*1974TG[21], NM_018287.7:c.*1974TG[22], NM_018287.7:c.*1974TG[23], NM_018287.7:c.*1974TG[24], NM_018287.7:c.*1974TG[25], NM_018287.7:c.*1974TG[26], NM_018287.7:c.*1974TG[27], NM_018287.7:c.*1974TG[28], NM_018287.7:c.*1974TG[29], NM_018287.6:c.*1974TG[6], NM_018287.6:c.*1974TG[7], NM_018287.6:c.*1974TG[8], NM_018287.6:c.*1974TG[9], NM_018287.6:c.*1974TG[10], NM_018287.6:c.*1974TG[11], NM_018287.6:c.*1974TG[12], NM_018287.6:c.*1974TG[13], NM_018287.6:c.*1974TG[14], NM_018287.6:c.*1974TG[15], NM_018287.6:c.*1974TG[16], NM_018287.6:c.*1974TG[17], NM_018287.6:c.*1974TG[19], NM_018287.6:c.*1974TG[20], NM_018287.6:c.*1974TG[21], NM_018287.6:c.*1974TG[22], NM_018287.6:c.*1974TG[23], NM_018287.6:c.*1974TG[24], NM_018287.6:c.*1974TG[25], NM_018287.6:c.*1974TG[26], NM_018287.6:c.*1974TG[27], NM_018287.6:c.*1974TG[28], NM_018287.6:c.*1974TG[29], XM_005252644.3:c.*1974TG[6], XM_005252644.3:c.*1974TG[7], XM_005252644.3:c.*1974TG[8], XM_005252644.3:c.*1974TG[9], XM_005252644.3:c.*1974TG[10], XM_005252644.3:c.*1974TG[11], XM_005252644.3:c.*1974TG[12], XM_005252644.3:c.*1974TG[13], XM_005252644.3:c.*1974TG[14], XM_005252644.3:c.*1974TG[15], XM_005252644.3:c.*1974TG[16], XM_005252644.3:c.*1974TG[17], XM_005252644.3:c.*1974TG[19], XM_005252644.3:c.*1974TG[20], XM_005252644.3:c.*1974TG[21], XM_005252644.3:c.*1974TG[22], XM_005252644.3:c.*1974TG[23], XM_005252644.3:c.*1974TG[24], XM_005252644.3:c.*1974TG[25], XM_005252644.3:c.*1974TG[26], XM_005252644.3:c.*1974TG[27], XM_005252644.3:c.*1974TG[28], XM_005252644.3:c.*1974TG[29], XM_005252644.2:c.*1974TG[6], XM_005252644.2:c.*1974TG[7], XM_005252644.2:c.*1974TG[8], XM_005252644.2:c.*1974TG[9], XM_005252644.2:c.*1974TG[10], XM_005252644.2:c.*1974TG[11], XM_005252644.2:c.*1974TG[12], XM_005252644.2:c.*1974TG[13], XM_005252644.2:c.*1974TG[14], XM_005252644.2:c.*1974TG[15], XM_005252644.2:c.*1974TG[16], XM_005252644.2:c.*1974TG[17], XM_005252644.2:c.*1974TG[19], XM_005252644.2:c.*1974TG[20], XM_005252644.2:c.*1974TG[21], XM_005252644.2:c.*1974TG[22], XM_005252644.2:c.*1974TG[23], XM_005252644.2:c.*1974TG[24], XM_005252644.2:c.*1974TG[25], XM_005252644.2:c.*1974TG[26], XM_005252644.2:c.*1974TG[27], XM_005252644.2:c.*1974TG[28], XM_005252644.2:c.*1974TG[29], XM_005252644.1:c.*1974TG[6], XM_005252644.1:c.*1974TG[7], XM_005252644.1:c.*1974TG[8], XM_005252644.1:c.*1974TG[9], XM_005252644.1:c.*1974TG[10], XM_005252644.1:c.*1974TG[11], XM_005252644.1:c.*1974TG[12], XM_005252644.1:c.*1974TG[13], XM_005252644.1:c.*1974TG[14], XM_005252644.1:c.*1974TG[15], XM_005252644.1:c.*1974TG[16], XM_005252644.1:c.*1974TG[17], XM_005252644.1:c.*1974TG[19], XM_005252644.1:c.*1974TG[20], XM_005252644.1:c.*1974TG[21], XM_005252644.1:c.*1974TG[22], XM_005252644.1:c.*1974TG[23], XM_005252644.1:c.*1974TG[24], XM_005252644.1:c.*1974TG[25], XM_005252644.1:c.*1974TG[26], XM_005252644.1:c.*1974TG[27], XM_005252644.1:c.*1974TG[28], XM_005252644.1:c.*1974TG[29], XM_011519761.3:c.*1974TG[6], XM_011519761.3:c.*1974TG[7], XM_011519761.3:c.*1974TG[8], XM_011519761.3:c.*1974TG[9], XM_011519761.3:c.*1974TG[10], XM_011519761.3:c.*1974TG[11], XM_011519761.3:c.*1974TG[12], XM_011519761.3:c.*1974TG[13], XM_011519761.3:c.*1974TG[14], XM_011519761.3:c.*1974TG[15], XM_011519761.3:c.*1974TG[16], XM_011519761.3:c.*1974TG[17], XM_011519761.3:c.*1974TG[19], XM_011519761.3:c.*1974TG[20], XM_011519761.3:c.*1974TG[21], XM_011519761.3:c.*1974TG[22], XM_011519761.3:c.*1974TG[23], XM_011519761.3:c.*1974TG[24], XM_011519761.3:c.*1974TG[25], XM_011519761.3:c.*1974TG[26], XM_011519761.3:c.*1974TG[27], XM_011519761.3:c.*1974TG[28], XM_011519761.3:c.*1974TG[29], XM_011519761.2:c.*1974TG[6], XM_011519761.2:c.*1974TG[7], XM_011519761.2:c.*1974TG[8], XM_011519761.2:c.*1974TG[9], XM_011519761.2:c.*1974TG[10], XM_011519761.2:c.*1974TG[11], XM_011519761.2:c.*1974TG[12], XM_011519761.2:c.*1974TG[13], XM_011519761.2:c.*1974TG[14], XM_011519761.2:c.*1974TG[15], XM_011519761.2:c.*1974TG[16], XM_011519761.2:c.*1974TG[17], XM_011519761.2:c.*1974TG[19], XM_011519761.2:c.*1974TG[20], XM_011519761.2:c.*1974TG[21], XM_011519761.2:c.*1974TG[22], XM_011519761.2:c.*1974TG[23], XM_011519761.2:c.*1974TG[24], XM_011519761.2:c.*1974TG[25], XM_011519761.2:c.*1974TG[26], XM_011519761.2:c.*1974TG[27], XM_011519761.2:c.*1974TG[28], XM_011519761.2:c.*1974TG[29], XM_011519761.1:c.*1974TG[6], XM_011519761.1:c.*1974TG[7], XM_011519761.1:c.*1974TG[8], XM_011519761.1:c.*1974TG[9], XM_011519761.1:c.*1974TG[10], XM_011519761.1:c.*1974TG[11], XM_011519761.1:c.*1974TG[12], XM_011519761.1:c.*1974TG[13], XM_011519761.1:c.*1974TG[14], XM_011519761.1:c.*1974TG[15], XM_011519761.1:c.*1974TG[16], XM_011519761.1:c.*1974TG[17], XM_011519761.1:c.*1974TG[19], XM_011519761.1:c.*1974TG[20], XM_011519761.1:c.*1974TG[21], XM_011519761.1:c.*1974TG[22], XM_011519761.1:c.*1974TG[23], XM_011519761.1:c.*1974TG[24], XM_011519761.1:c.*1974TG[25], XM_011519761.1:c.*1974TG[26], XM_011519761.1:c.*1974TG[27], XM_011519761.1:c.*1974TG[28], XM_011519761.1:c.*1974TG[29], XM_017016954.3:c.*1974TG[6], XM_017016954.3:c.*1974TG[7], XM_017016954.3:c.*1974TG[8], XM_017016954.3:c.*1974TG[9], XM_017016954.3:c.*1974TG[10], XM_017016954.3:c.*1974TG[11], XM_017016954.3:c.*1974TG[12], XM_017016954.3:c.*1974TG[13], XM_017016954.3:c.*1974TG[14], XM_017016954.3:c.*1974TG[15], XM_017016954.3:c.*1974TG[16], XM_017016954.3:c.*1974TG[17], XM_017016954.3:c.*1974TG[19], XM_017016954.3:c.*1974TG[20], XM_017016954.3:c.*1974TG[21], XM_017016954.3:c.*1974TG[22], XM_017016954.3:c.*1974TG[23], XM_017016954.3:c.*1974TG[24], XM_017016954.3:c.*1974TG[25], XM_017016954.3:c.*1974TG[26], XM_017016954.3:c.*1974TG[27], XM_017016954.3:c.*1974TG[28], XM_017016954.3:c.*1974TG[29], XM_017016954.2:c.*1974TG[6], XM_017016954.2:c.*1974TG[7], XM_017016954.2:c.*1974TG[8], XM_017016954.2:c.*1974TG[9], XM_017016954.2:c.*1974TG[10], XM_017016954.2:c.*1974TG[11], XM_017016954.2:c.*1974TG[12], XM_017016954.2:c.*1974TG[13], XM_017016954.2:c.*1974TG[14], XM_017016954.2:c.*1974TG[15], XM_017016954.2:c.*1974TG[16], XM_017016954.2:c.*1974TG[17], XM_017016954.2:c.*1974TG[19], XM_017016954.2:c.*1974TG[20], XM_017016954.2:c.*1974TG[21], XM_017016954.2:c.*1974TG[22], XM_017016954.2:c.*1974TG[23], XM_017016954.2:c.*1974TG[24], XM_017016954.2:c.*1974TG[25], XM_017016954.2:c.*1974TG[26], XM_017016954.2:c.*1974TG[27], XM_017016954.2:c.*1974TG[28], XM_017016954.2:c.*1974TG[29], XM_017016954.1:c.*1974TG[6], XM_017016954.1:c.*1974TG[7], XM_017016954.1:c.*1974TG[8], XM_017016954.1:c.*1974TG[9], XM_017016954.1:c.*1974TG[10], XM_017016954.1:c.*1974TG[11], XM_017016954.1:c.*1974TG[12], XM_017016954.1:c.*1974TG[13], XM_017016954.1:c.*1974TG[14], XM_017016954.1:c.*1974TG[15], XM_017016954.1:c.*1974TG[16], XM_017016954.1:c.*1974TG[17], XM_017016954.1:c.*1974TG[19], XM_017016954.1:c.*1974TG[20], XM_017016954.1:c.*1974TG[21], XM_017016954.1:c.*1974TG[22], XM_017016954.1:c.*1974TG[23], XM_017016954.1:c.*1974TG[24], XM_017016954.1:c.*1974TG[25], XM_017016954.1:c.*1974TG[26], XM_017016954.1:c.*1974TG[27], XM_017016954.1:c.*1974TG[28], XM_017016954.1:c.*1974TG[29], NM_001270696.2:c.*1974TG[6], NM_001270696.2:c.*1974TG[7], NM_001270696.2:c.*1974TG[8], NM_001270696.2:c.*1974TG[9], NM_001270696.2:c.*1974TG[10], NM_001270696.2:c.*1974TG[11], NM_001270696.2:c.*1974TG[12], NM_001270696.2:c.*1974TG[13], NM_001270696.2:c.*1974TG[14], NM_001270696.2:c.*1974TG[15], NM_001270696.2:c.*1974TG[16], NM_001270696.2:c.*1974TG[17], NM_001270696.2:c.*1974TG[19], NM_001270696.2:c.*1974TG[20], NM_001270696.2:c.*1974TG[21], NM_001270696.2:c.*1974TG[22], NM_001270696.2:c.*1974TG[23], NM_001270696.2:c.*1974TG[24], NM_001270696.2:c.*1974TG[25], NM_001270696.2:c.*1974TG[26], NM_001270696.2:c.*1974TG[27], NM_001270696.2:c.*1974TG[28], NM_001270696.2:c.*1974TG[29], NM_001270696.1:c.*1974TG[6], NM_001270696.1:c.*1974TG[7], NM_001270696.1:c.*1974TG[8], NM_001270696.1:c.*1974TG[9], NM_001270696.1:c.*1974TG[10], NM_001270696.1:c.*1974TG[11], NM_001270696.1:c.*1974TG[12], NM_001270696.1:c.*1974TG[13], NM_001270696.1:c.*1974TG[14], NM_001270696.1:c.*1974TG[15], NM_001270696.1:c.*1974TG[16], NM_001270696.1:c.*1974TG[17], NM_001270696.1:c.*1974TG[19], NM_001270696.1:c.*1974TG[20], NM_001270696.1:c.*1974TG[21], NM_001270696.1:c.*1974TG[22], NM_001270696.1:c.*1974TG[23], NM_001270696.1:c.*1974TG[24], NM_001270696.1:c.*1974TG[25], NM_001270696.1:c.*1974TG[26], NM_001270696.1:c.*1974TG[27], NM_001270696.1:c.*1974TG[28], NM_001270696.1:c.*1974TG[29], NM_001270698.2:c.*1974TG[6], NM_001270698.2:c.*1974TG[7], NM_001270698.2:c.*1974TG[8], NM_001270698.2:c.*1974TG[9], NM_001270698.2:c.*1974TG[10], NM_001270698.2:c.*1974TG[11], NM_001270698.2:c.*1974TG[12], NM_001270698.2:c.*1974TG[13], NM_001270698.2:c.*1974TG[14], NM_001270698.2:c.*1974TG[15], NM_001270698.2:c.*1974TG[16], NM_001270698.2:c.*1974TG[17], NM_001270698.2:c.*1974TG[19], NM_001270698.2:c.*1974TG[20], NM_001270698.2:c.*1974TG[21], NM_001270698.2:c.*1974TG[22], NM_001270698.2:c.*1974TG[23], NM_001270698.2:c.*1974TG[24], NM_001270698.2:c.*1974TG[25], NM_001270698.2:c.*1974TG[26], NM_001270698.2:c.*1974TG[27], NM_001270698.2:c.*1974TG[28], NM_001270698.2:c.*1974TG[29], NM_001270698.1:c.*1974TG[6], NM_001270698.1:c.*1974TG[7], NM_001270698.1:c.*1974TG[8], NM_001270698.1:c.*1974TG[9], NM_001270698.1:c.*1974TG[10], NM_001270698.1:c.*1974TG[11], NM_001270698.1:c.*1974TG[12], NM_001270698.1:c.*1974TG[13], NM_001270698.1:c.*1974TG[14], NM_001270698.1:c.*1974TG[15], NM_001270698.1:c.*1974TG[16], NM_001270698.1:c.*1974TG[17], NM_001270698.1:c.*1974TG[19], NM_001270698.1:c.*1974TG[20], NM_001270698.1:c.*1974TG[21], NM_001270698.1:c.*1974TG[22], NM_001270698.1:c.*1974TG[23], NM_001270698.1:c.*1974TG[24], NM_001270698.1:c.*1974TG[25], NM_001270698.1:c.*1974TG[26], NM_001270698.1:c.*1974TG[27], NM_001270698.1:c.*1974TG[28], NM_001270698.1:c.*1974TG[29], NM_001270695.1:c.*1974TG[6], NM_001270695.1:c.*1974TG[7], NM_001270695.1:c.*1974TG[8], NM_001270695.1:c.*1974TG[9], NM_001270695.1:c.*1974TG[10], NM_001270695.1:c.*1974TG[11], NM_001270695.1:c.*1974TG[12], NM_001270695.1:c.*1974TG[13], NM_001270695.1:c.*1974TG[14], NM_001270695.1:c.*1974TG[15], NM_001270695.1:c.*1974TG[16], NM_001270695.1:c.*1974TG[17], NM_001270695.1:c.*1974TG[19], NM_001270695.1:c.*1974TG[20], NM_001270695.1:c.*1974TG[21], NM_001270695.1:c.*1974TG[22], NM_001270695.1:c.*1974TG[23], NM_001270695.1:c.*1974TG[24], NM_001270695.1:c.*1974TG[25], NM_001270695.1:c.*1974TG[26], NM_001270695.1:c.*1974TG[27], NM_001270695.1:c.*1974TG[28], NM_001270695.1:c.*1974TG[29], NM_001270697.1:c.*1974TG[6], NM_001270697.1:c.*1974TG[7], NM_001270697.1:c.*1974TG[8], NM_001270697.1:c.*1974TG[9], NM_001270697.1:c.*1974TG[10], NM_001270697.1:c.*1974TG[11], NM_001270697.1:c.*1974TG[12], NM_001270697.1:c.*1974TG[13], NM_001270697.1:c.*1974TG[14], NM_001270697.1:c.*1974TG[15], NM_001270697.1:c.*1974TG[16], NM_001270697.1:c.*1974TG[17], NM_001270697.1:c.*1974TG[19], NM_001270697.1:c.*1974TG[20], NM_001270697.1:c.*1974TG[21], NM_001270697.1:c.*1974TG[22], NM_001270697.1:c.*1974TG[23], NM_001270697.1:c.*1974TG[24], NM_001270697.1:c.*1974TG[25], NM_001270697.1:c.*1974TG[26], NM_001270697.1:c.*1974TG[27], NM_001270697.1:c.*1974TG[28], NM_001270697.1:c.*1974TG[29], XM_047426021.1:c.*1974TG[6], XM_047426021.1:c.*1974TG[7], XM_047426021.1:c.*1974TG[8], XM_047426021.1:c.*1974TG[9], XM_047426021.1:c.*1974TG[10], XM_047426021.1:c.*1974TG[11], XM_047426021.1:c.*1974TG[12], XM_047426021.1:c.*1974TG[13], XM_047426021.1:c.*1974TG[14], XM_047426021.1:c.*1974TG[15], XM_047426021.1:c.*1974TG[16], XM_047426021.1:c.*1974TG[17], XM_047426021.1:c.*1974TG[19], XM_047426021.1:c.*1974TG[20], XM_047426021.1:c.*1974TG[21], XM_047426021.1:c.*1974TG[22], XM_047426021.1:c.*1974TG[23], XM_047426021.1:c.*1974TG[24], XM_047426021.1:c.*1974TG[25], XM_047426021.1:c.*1974TG[26], XM_047426021.1:c.*1974TG[27], XM_047426021.1:c.*1974TG[28], XM_047426021.1:c.*1974TG[29], NM_001270699.1:c.*1974TG[6], NM_001270699.1:c.*1974TG[7], NM_001270699.1:c.*1974TG[8], NM_001270699.1:c.*1974TG[9], NM_001270699.1:c.*1974TG[10], NM_001270699.1:c.*1974TG[11], NM_001270699.1:c.*1974TG[12], NM_001270699.1:c.*1974TG[13], NM_001270699.1:c.*1974TG[14], NM_001270699.1:c.*1974TG[15], NM_001270699.1:c.*1974TG[16], NM_001270699.1:c.*1974TG[17], NM_001270699.1:c.*1974TG[19], NM_001270699.1:c.*1974TG[20], NM_001270699.1:c.*1974TG[21], NM_001270699.1:c.*1974TG[22], NM_001270699.1:c.*1974TG[23], NM_001270699.1:c.*1974TG[24], NM_001270699.1:c.*1974TG[25], NM_001270699.1:c.*1974TG[26], NM_001270699.1:c.*1974TG[27], NM_001270699.1:c.*1974TG[28], NM_001270699.1:c.*1974TG[29]

Select item 148260819716.

rs1482608197 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:31807756 (GRCh38)
10:32096684 (GRCh37)
Canonical SPDI:: NC_000010.11:31807755:G:A
Gene:: ARHGAP12 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000010.11:g.31807756G>A, NC_000010.10:g.32096684G>A, NM_018287.7:c.2443C>T, NM_018287.6:c.2443C>T, XM_005252644.3:c.2287C>T, XM_005252644.2:c.2287C>T, XM_005252644.1:c.2287C>T, XM_011519761.3:c.2221C>T, XM_011519761.2:c.2221C>T, XM_011519761.1:c.2221C>T, XM_017016954.3:c.2131C>T, XM_017016954.2:c.2131C>T, XM_017016954.1:c.2131C>T, NM_001270696.2:c.2353C>T, NM_001270696.1:c.2353C>T, NM_001270698.2:c.2212C>T, NM_001270698.1:c.2212C>T, NM_001270695.1:c.2428C>T, NM_001270697.1:c.2302C>T, XM_047426021.1:c.2206C>T, NM_001270699.1:c.2287C>T, NP_060757.4:p.Pro815Ser, XP_005252701.1:p.Pro763Ser, XP_011518063.1:p.Pro741Ser, XP_016872443.1:p.Pro711Ser, NP_001257625.1:p.Pro785Ser, NP_001257627.1:p.Pro738Ser, NP_001257624.1:p.Pro810Ser, NP_001257626.1:p.Pro768Ser, XP_047281977.1:p.Pro736Ser, NP_001257628.1:p.Pro763Ser

Select item 148251828917.

rs1482518289 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:31908419 (GRCh38)
10:32197347 (GRCh37)
Canonical SPDI:: NC_000010.11:31908418:A:C
Gene:: ARHGAP12 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.31908419A>C, NC_000010.10:g.32197347A>C, NM_018287.7:c.437T>G, NM_018287.6:c.437T>G, XM_005252644.3:c.437T>G, XM_005252644.2:c.437T>G, XM_005252644.1:c.437T>G, XM_011519761.3:c.437T>G, XM_011519761.2:c.437T>G, XM_011519761.1:c.437T>G, XM_017016954.3:c.437T>G, XM_017016954.2:c.437T>G, XM_017016954.1:c.437T>G, NM_001270696.2:c.437T>G, NM_001270696.1:c.437T>G, NM_001270698.2:c.437T>G, NM_001270698.1:c.437T>G, NM_001270695.1:c.437T>G, NM_001270697.1:c.437T>G, XM_047426021.1:c.437T>G, NM_001270699.1:c.437T>G, NP_060757.4:p.Val146Gly, XP_005252701.1:p.Val146Gly, XP_011518063.1:p.Val146Gly, XP_016872443.1:p.Val146Gly, NP_001257625.1:p.Val146Gly, NP_001257627.1:p.Val146Gly, NP_001257624.1:p.Val146Gly, NP_001257626.1:p.Val146Gly, XP_047281977.1:p.Val146Gly, NP_001257628.1:p.Val146Gly

Select item 148226903218.

rs1482269032 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:31812707 (GRCh38)
10:32101635 (GRCh37)
Canonical SPDI:: NC_000010.11:31812706:C:T
Gene:: ARHGAP12 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.31812707C>T, NC_000010.10:g.32101635C>T, NM_018287.7:c.1951G>A, NM_018287.6:c.1951G>A, XM_005252644.3:c.1795G>A, XM_005252644.2:c.1795G>A, XM_005252644.1:c.1795G>A, XM_011519761.3:c.1729G>A, XM_011519761.2:c.1729G>A, XM_011519761.1:c.1729G>A, XM_017016954.3:c.1639G>A, XM_017016954.2:c.1639G>A, XM_017016954.1:c.1639G>A, NM_001270696.2:c.1861G>A, NM_001270696.1:c.1861G>A, NM_001270698.2:c.1720G>A, NM_001270698.1:c.1720G>A, NM_001270695.1:c.1936G>A, NM_001270697.1:c.1810G>A, XM_047426021.1:c.1714G>A, NM_001270699.1:c.1795G>A, NP_060757.4:p.Asp651Asn, XP_005252701.1:p.Asp599Asn, XP_011518063.1:p.Asp577Asn, XP_016872443.1:p.Asp547Asn, NP_001257625.1:p.Asp621Asn, NP_001257627.1:p.Asp574Asn, NP_001257624.1:p.Asp646Asn, NP_001257626.1:p.Asp604Asn, XP_047281977.1:p.Asp572Asn, NP_001257628.1:p.Asp599Asn

Select item 148196628119.

rs1481966281 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 10:31814321 (GRCh38)
10:32103249 (GRCh37)
Canonical SPDI:: NC_000010.11:31814320:T:G
Gene:: ARHGAP12 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.31814321T>G, NC_000010.10:g.32103249T>G, NM_018287.7:c.1772A>C, NM_018287.6:c.1772A>C, XM_005252644.3:c.1616A>C, XM_005252644.2:c.1616A>C, XM_005252644.1:c.1616A>C, XM_011519761.3:c.1550A>C, XM_011519761.2:c.1550A>C, XM_011519761.1:c.1550A>C, XM_017016954.3:c.1460A>C, XM_017016954.2:c.1460A>C, XM_017016954.1:c.1460A>C, NM_001270696.2:c.1682A>C, NM_001270696.1:c.1682A>C, NM_001270698.2:c.1541A>C, NM_001270698.1:c.1541A>C, NM_001270695.1:c.1757A>C, NM_001270697.1:c.1631A>C, XM_047426021.1:c.1535A>C, NM_001270699.1:c.1616A>C, NP_060757.4:p.Asp591Ala, XP_005252701.1:p.Asp539Ala, XP_011518063.1:p.Asp517Ala, XP_016872443.1:p.Asp487Ala, NP_001257625.1:p.Asp561Ala, NP_001257627.1:p.Asp514Ala, NP_001257624.1:p.Asp586Ala, NP_001257626.1:p.Asp544Ala, XP_047281977.1:p.Asp512Ala, NP_001257628.1:p.Asp539Ala

Select item 148052854820.

rs1480528548 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:31806711 (GRCh38)
10:32095639 (GRCh37)
Canonical SPDI:: NC_000010.11:31806710:C:T
Gene:: ARHGAP12 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.31806711C>T, NC_000010.10:g.32095639C>T, NM_018287.7:c.*947G>A, NM_018287.6:c.*947G>A, XM_005252644.3:c.*947G>A, XM_005252644.2:c.*947G>A, XM_005252644.1:c.*947G>A, XM_011519761.3:c.*947G>A, XM_011519761.2:c.*947G>A, XM_011519761.1:c.*947G>A, XM_017016954.3:c.*947G>A, XM_017016954.2:c.*947G>A, XM_017016954.1:c.*947G>A, NM_001270696.2:c.*947G>A, NM_001270696.1:c.*947G>A, NM_001270698.2:c.*947G>A, NM_001270698.1:c.*947G>A, NM_001270695.1:c.*947G>A, NM_001270697.1:c.*947G>A, XM_047426021.1:c.*947G>A, NM_001270699.1:c.*947G>A

<< First< Prev

Page of 60

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 1197

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity