SNP Links for Protein (Select 304361762) - SNP

Select item 14740196051.

rs1474019605 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:31915973 (GRCh38)
1:32381574 (GRCh37)
Canonical SPDI:: NC_000001.11:31915972:A:G
Gene:: PTP4A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.31915973A>G, NC_000001.10:g.32381574A>G, NM_080391.4:c.111T>C, NM_080391.3:c.111T>C, NM_001195100.2:c.111T>C, NM_001195100.1:c.111T>C, NM_003479.2:c.111T>C, NM_080392.2:c.111T>C, NM_001369859.1:c.111T>C, NM_001369860.1:c.111T>C, XM_047431030.1:c.111T>C, XM_047431017.1:c.111T>C, XM_047431024.1:c.111T>C, XM_047431028.1:c.111T>C, XM_047431032.1:c.111T>C, NM_080392.1:c.111T>C, NM_003479.1:c.111T>C

Select item 14735972642.

rs1473597264 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:31918982 (GRCh38)
1:32384583 (GRCh37)
Canonical SPDI:: NC_000001.11:31918981:G:A
Gene:: PTP4A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.31918982G>A, NC_000001.10:g.32384583G>A, NM_080391.4:c.84C>T, NM_080391.3:c.84C>T, NM_001195100.2:c.84C>T, NM_001195100.1:c.84C>T, NM_001195101.2:c.84C>T, NM_001195101.1:c.84C>T, NM_003479.2:c.84C>T, NM_080392.2:c.84C>T, NM_001369859.1:c.84C>T, NM_001369860.1:c.84C>T, NM_001369858.1:c.84C>T, XM_047431030.1:c.84C>T, XM_047431017.1:c.84C>T, XM_047431024.1:c.84C>T, XM_047431039.1:c.84C>T, XM_047431028.1:c.84C>T, XM_047431032.1:c.84C>T, XM_047431035.1:c.84C>T, NM_080392.1:c.84C>T, NM_003479.1:c.84C>T

Select item 14722490223.

rs1472249022 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:31915953 (GRCh38)
1:32381554 (GRCh37)
Canonical SPDI:: NC_000001.11:31915952:C:T
Gene:: PTP4A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.31915953C>T, NC_000001.10:g.32381554C>T, NM_080391.4:c.131G>A, NM_080391.3:c.131G>A, NM_001195100.2:c.131G>A, NM_001195100.1:c.131G>A, NM_003479.2:c.131G>A, NM_080392.2:c.131G>A, NM_001369859.1:c.131G>A, NM_001369860.1:c.131G>A, XM_047431030.1:c.131G>A, XM_047431017.1:c.131G>A, XM_047431024.1:c.131G>A, XM_047431028.1:c.131G>A, XM_047431032.1:c.131G>A, NM_080392.1:c.131G>A, NM_003479.1:c.131G>A, NP_536316.1:p.Arg44Gln, NP_001182029.1:p.Arg44Gln, NP_001356788.1:p.Arg44Gln, NP_001356789.1:p.Arg44Gln, XP_047286986.1:p.Arg44Gln, XP_047286973.1:p.Arg44Gln, XP_047286980.1:p.Arg44Gln, XP_047286984.1:p.Arg44Gln, XP_047286988.1:p.Arg44Gln

Select item 14700085374.

rs1470008537 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:31908870 (GRCh38)
1:32374471 (GRCh37)
Canonical SPDI:: NC_000001.11:31908869:C:A
Gene:: PTP4A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.31908870C>A, NC_000001.10:g.32374471C>A, NM_080391.4:c.486G>T, NM_080391.3:c.486G>T, NM_001195100.2:c.411G>T, NM_001195100.1:c.411G>T, NM_001195101.2:c.393G>T, NM_001195101.1:c.393G>T, NM_003479.2:c.486G>T, NM_080392.2:c.*31G>T, NM_001369859.1:c.486G>T, NM_001369860.1:c.486G>T, NM_001369858.1:c.393G>T, XM_047431030.1:c.486G>T, XM_047431017.1:c.486G>T, XM_047431024.1:c.486G>T, XM_047431039.1:c.393G>T, XM_047431028.1:c.486G>T, XM_047431032.1:c.411G>T, XM_047431035.1:c.393G>T, NM_080392.1:c.*31G>T, NM_003479.1:c.486G>T

Select item 14544984605.

rs1454498460 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:31908909 (GRCh38)
1:32374510 (GRCh37)
Canonical SPDI:: NC_000001.11:31908908:G:A
Gene:: PTP4A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0.000111/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.31908909G>A, NC_000001.10:g.32374510G>A, NM_080391.4:c.447C>T, NM_080391.3:c.447C>T, NM_001195100.2:c.372C>T, NM_001195100.1:c.372C>T, NM_001195101.2:c.354C>T, NM_001195101.1:c.354C>T, NM_003479.2:c.447C>T, NM_080392.2:c.241C>T, NM_001369859.1:c.447C>T, NM_001369860.1:c.447C>T, NM_001369858.1:c.354C>T, XM_047431030.1:c.447C>T, XM_047431017.1:c.447C>T, XM_047431024.1:c.447C>T, XM_047431039.1:c.354C>T, XM_047431028.1:c.447C>T, XM_047431032.1:c.372C>T, XM_047431035.1:c.354C>T, NM_080392.1:c.241C>T, NM_003479.1:c.447C>T

Select item 14505374246.

rs1450537424 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:31919006 (GRCh38)
1:32384607 (GRCh37)
Canonical SPDI:: NC_000001.11:31919005:G:A
Gene:: PTP4A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.31919006G>A, NC_000001.10:g.32384607G>A, NM_080391.4:c.60C>T, NM_080391.3:c.60C>T, NM_001195100.2:c.60C>T, NM_001195100.1:c.60C>T, NM_001195101.2:c.60C>T, NM_001195101.1:c.60C>T, NM_003479.2:c.60C>T, NM_080392.2:c.60C>T, NM_001369859.1:c.60C>T, NM_001369860.1:c.60C>T, NM_001369858.1:c.60C>T, XM_047431030.1:c.60C>T, XM_047431017.1:c.60C>T, XM_047431024.1:c.60C>T, XM_047431039.1:c.60C>T, XM_047431028.1:c.60C>T, XM_047431032.1:c.60C>T, XM_047431035.1:c.60C>T, NM_080392.1:c.60C>T, NM_003479.1:c.60C>T

Select item 14000890127.

rs1400089012 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:31908933 (GRCh38)
1:32374534 (GRCh37)
Canonical SPDI:: NC_000001.11:31908932:T:C
Gene:: PTP4A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.31908933T>C, NC_000001.10:g.32374534T>C, NM_080391.4:c.423A>G, NM_080391.3:c.423A>G, NM_001195100.2:c.348A>G, NM_001195100.1:c.348A>G, NM_001195101.2:c.330A>G, NM_001195101.1:c.330A>G, NM_003479.2:c.423A>G, NM_080392.2:c.217A>G, NM_001369859.1:c.423A>G, NM_001369860.1:c.423A>G, NM_001369858.1:c.330A>G, XM_047431030.1:c.423A>G, XM_047431017.1:c.423A>G, XM_047431024.1:c.423A>G, XM_047431039.1:c.330A>G, XM_047431028.1:c.423A>G, XM_047431032.1:c.348A>G, XM_047431035.1:c.330A>G, NM_080392.1:c.217A>G, NM_003479.1:c.423A>G

Select item 13978113078.

rs1397811307 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:31911768 (GRCh38)
1:32377369 (GRCh37)
Canonical SPDI:: NC_000001.11:31911767:T:C
Gene:: PTP4A2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.31911768T>C, NC_000001.10:g.32377369T>C, NM_080391.4:c.248A>G, NM_080391.3:c.248A>G, NM_001195100.2:c.248A>G, NM_001195100.1:c.248A>G, NM_001195101.2:c.155A>G, NM_001195101.1:c.155A>G, NM_003479.2:c.248A>G, NM_001369859.1:c.248A>G, NM_001369860.1:c.248A>G, NM_001369858.1:c.155A>G, XM_047431030.1:c.248A>G, XM_047431017.1:c.248A>G, XM_047431024.1:c.248A>G, XM_047431039.1:c.155A>G, XM_047431028.1:c.248A>G, XM_047431032.1:c.248A>G, XM_047431035.1:c.155A>G, NM_003479.1:c.248A>G, NP_536316.1:p.Asn83Ser, NP_001182029.1:p.Asn83Ser, NP_001182030.1:p.Asn52Ser, NP_001356788.1:p.Asn83Ser, NP_001356789.1:p.Asn83Ser, NP_001356787.1:p.Asn52Ser, XP_047286986.1:p.Asn83Ser, XP_047286973.1:p.Asn83Ser, XP_047286980.1:p.Asn83Ser, XP_047286995.1:p.Asn52Ser, XP_047286984.1:p.Asn83Ser, XP_047286988.1:p.Asn83Ser, XP_047286991.1:p.Asn52Ser

Select item 13959235419.

rs1395923541 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 1:31915907 (GRCh38)
1:32381508 (GRCh37)
Canonical SPDI:: NC_000001.11:31915906:T:C,NC_000001.11:31915906:T:G
Gene:: PTP4A2 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.31915907T>C, NC_000001.11:g.31915907T>G, NC_000001.10:g.32381508T>C, NC_000001.10:g.32381508T>G, NM_080391.4:c.177A>G, NM_080391.4:c.177A>C, NM_080391.3:c.177A>G, NM_080391.3:c.177A>C, NM_001195100.2:c.177A>G, NM_001195100.2:c.177A>C, NM_001195100.1:c.177A>G, NM_001195100.1:c.177A>C, NM_003479.2:c.177A>G, NM_003479.2:c.177A>C, NM_080392.2:c.177A>G, NM_080392.2:c.177A>C, NM_001369859.1:c.177A>G, NM_001369859.1:c.177A>C, NM_001369860.1:c.177A>G, NM_001369860.1:c.177A>C, XM_047431030.1:c.177A>G, XM_047431030.1:c.177A>C, XM_047431017.1:c.177A>G, XM_047431017.1:c.177A>C, XM_047431024.1:c.177A>G, XM_047431024.1:c.177A>C, XM_047431028.1:c.177A>G, XM_047431028.1:c.177A>C, XM_047431032.1:c.177A>G, XM_047431032.1:c.177A>C, NM_080392.1:c.177A>G, NM_080392.1:c.177A>C, NM_003479.1:c.177A>G, NM_003479.1:c.177A>C

Select item 138320022010.

rs1383200220 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:31915964 (GRCh38)
1:32381565 (GRCh37)
Canonical SPDI:: NC_000001.11:31915963:C:T
Gene:: PTP4A2 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.31915964C>T, NC_000001.10:g.32381565C>T, NM_080391.4:c.120G>A, NM_080391.3:c.120G>A, NM_001195100.2:c.120G>A, NM_001195100.1:c.120G>A, NM_003479.2:c.120G>A, NM_080392.2:c.120G>A, NM_001369859.1:c.120G>A, NM_001369860.1:c.120G>A, XM_047431030.1:c.120G>A, XM_047431017.1:c.120G>A, XM_047431024.1:c.120G>A, XM_047431028.1:c.120G>A, XM_047431032.1:c.120G>A, NM_080392.1:c.120G>A, NM_003479.1:c.120G>A

Select item 138112693211.

rs1381126932 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:31919048 (GRCh38)
1:32384649 (GRCh37)
Canonical SPDI:: NC_000001.11:31919047:A:C
Gene:: PTP4A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by cluster
HGVS:: NC_000001.11:g.31919048A>C, NC_000001.10:g.32384649A>C, NM_080391.4:c.18T>G, NM_080391.3:c.18T>G, NM_001195100.2:c.18T>G, NM_001195100.1:c.18T>G, NM_001195101.2:c.18T>G, NM_001195101.1:c.18T>G, NM_003479.2:c.18T>G, NM_080392.2:c.18T>G, NM_001369859.1:c.18T>G, NM_001369860.1:c.18T>G, NM_001369858.1:c.18T>G, XM_047431030.1:c.18T>G, XM_047431017.1:c.18T>G, XM_047431024.1:c.18T>G, XM_047431039.1:c.18T>G, XM_047431028.1:c.18T>G, XM_047431032.1:c.18T>G, XM_047431035.1:c.18T>G, NM_080392.1:c.18T>G, NM_003479.1:c.18T>G

Select item 137295877912.

rs1372958779 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:31918996 (GRCh38)
1:32384597 (GRCh37)
Canonical SPDI:: NC_000001.11:31918995:T:C
Gene:: PTP4A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000012/3 (GnomAD_exomes)
C=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.31918996T>C, NC_000001.10:g.32384597T>C, NM_080391.4:c.70A>G, NM_080391.3:c.70A>G, NM_001195100.2:c.70A>G, NM_001195100.1:c.70A>G, NM_001195101.2:c.70A>G, NM_001195101.1:c.70A>G, NM_003479.2:c.70A>G, NM_080392.2:c.70A>G, NM_001369859.1:c.70A>G, NM_001369860.1:c.70A>G, NM_001369858.1:c.70A>G, XM_047431030.1:c.70A>G, XM_047431017.1:c.70A>G, XM_047431024.1:c.70A>G, XM_047431039.1:c.70A>G, XM_047431028.1:c.70A>G, XM_047431032.1:c.70A>G, XM_047431035.1:c.70A>G, NM_080392.1:c.70A>G, NM_003479.1:c.70A>G, NP_536316.1:p.Asn24Asp, NP_001182029.1:p.Asn24Asp, NP_001182030.1:p.Asn24Asp, NP_001356788.1:p.Asn24Asp, NP_001356789.1:p.Asn24Asp, NP_001356787.1:p.Asn24Asp, XP_047286986.1:p.Asn24Asp, XP_047286973.1:p.Asn24Asp, XP_047286980.1:p.Asn24Asp, XP_047286995.1:p.Asn24Asp, XP_047286984.1:p.Asn24Asp, XP_047286988.1:p.Asn24Asp, XP_047286991.1:p.Asn24Asp

Select item 134651566713.

rs1346515667 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:31908958 (GRCh38)
1:32374559 (GRCh37)
Canonical SPDI:: NC_000001.11:31908957:T:C
Gene:: PTP4A2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.31908958T>C, NC_000001.10:g.32374559T>C, NM_080391.4:c.398A>G, NM_080391.3:c.398A>G, NM_001195100.2:c.323A>G, NM_001195100.1:c.323A>G, NM_001195101.2:c.305A>G, NM_001195101.1:c.305A>G, NM_003479.2:c.398A>G, NM_080392.2:c.192A>G, NM_001369859.1:c.398A>G, NM_001369860.1:c.398A>G, NM_001369858.1:c.305A>G, XM_047431030.1:c.398A>G, XM_047431017.1:c.398A>G, XM_047431024.1:c.398A>G, XM_047431039.1:c.305A>G, XM_047431028.1:c.398A>G, XM_047431032.1:c.323A>G, XM_047431035.1:c.305A>G, NM_080392.1:c.192A>G, NM_003479.1:c.398A>G, NP_536316.1:p.Lys133Arg, NP_001182029.1:p.Lys108Arg, NP_001182030.1:p.Lys102Arg, NP_001356788.1:p.Lys133Arg, NP_001356789.1:p.Lys133Arg, NP_001356787.1:p.Lys102Arg, XP_047286986.1:p.Lys133Arg, XP_047286973.1:p.Lys133Arg, XP_047286980.1:p.Lys133Arg, XP_047286995.1:p.Lys102Arg, XP_047286984.1:p.Lys133Arg, XP_047286988.1:p.Lys108Arg, XP_047286991.1:p.Lys102Arg

Select item 134567959714.

rs1345679597 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:31919043 (GRCh38)
1:32384644 (GRCh37)
Canonical SPDI:: NC_000001.11:31919042:T:A
Gene:: PTP4A2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.31919043T>A, NC_000001.10:g.32384644T>A, NM_080391.4:c.23A>T, NM_080391.3:c.23A>T, NM_001195100.2:c.23A>T, NM_001195100.1:c.23A>T, NM_001195101.2:c.23A>T, NM_001195101.1:c.23A>T, NM_003479.2:c.23A>T, NM_080392.2:c.23A>T, NM_001369859.1:c.23A>T, NM_001369860.1:c.23A>T, NM_001369858.1:c.23A>T, XM_047431030.1:c.23A>T, XM_047431017.1:c.23A>T, XM_047431024.1:c.23A>T, XM_047431039.1:c.23A>T, XM_047431028.1:c.23A>T, XM_047431032.1:c.23A>T, XM_047431035.1:c.23A>T, NM_080392.1:c.23A>T, NM_003479.1:c.23A>T, NP_536316.1:p.Glu8Val, NP_001182029.1:p.Glu8Val, NP_001182030.1:p.Glu8Val, NP_001356788.1:p.Glu8Val, NP_001356789.1:p.Glu8Val, NP_001356787.1:p.Glu8Val, XP_047286986.1:p.Glu8Val, XP_047286973.1:p.Glu8Val, XP_047286980.1:p.Glu8Val, XP_047286995.1:p.Glu8Val, XP_047286984.1:p.Glu8Val, XP_047286988.1:p.Glu8Val, XP_047286991.1:p.Glu8Val

Select item 134554825415.

rs1345548254 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:31911812 (GRCh38)
1:32377413 (GRCh37)
Canonical SPDI:: NC_000001.11:31911811:A:C
Gene:: PTP4A2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000046/2 (ALFA)
C=0.000009/2 (GnomAD_exomes)
C=0.000019/5 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000001.11:g.31911812A>C, NC_000001.10:g.32377413A>C, NM_080391.4:c.204T>G, NM_080391.3:c.204T>G, NM_001195100.2:c.204T>G, NM_001195100.1:c.204T>G, NM_001195101.2:c.111T>G, NM_001195101.1:c.111T>G, NM_003479.2:c.204T>G, NM_001369859.1:c.204T>G, NM_001369860.1:c.204T>G, NM_001369858.1:c.111T>G, XM_047431030.1:c.204T>G, XM_047431017.1:c.204T>G, XM_047431024.1:c.204T>G, XM_047431039.1:c.111T>G, XM_047431028.1:c.204T>G, XM_047431032.1:c.204T>G, XM_047431035.1:c.111T>G, NM_003479.1:c.204T>G, NP_536316.1:p.Asp68Glu, NP_001182029.1:p.Asp68Glu, NP_001182030.1:p.Asp37Glu, NP_001356788.1:p.Asp68Glu, NP_001356789.1:p.Asp68Glu, NP_001356787.1:p.Asp37Glu, XP_047286986.1:p.Asp68Glu, XP_047286973.1:p.Asp68Glu, XP_047286980.1:p.Asp68Glu, XP_047286995.1:p.Asp37Glu, XP_047286984.1:p.Asp68Glu, XP_047286988.1:p.Asp68Glu, XP_047286991.1:p.Asp37Glu

Select item 134111491516.

rs1341114915 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:31919018 (GRCh38)
1:32384619 (GRCh37)
Canonical SPDI:: NC_000001.11:31919017:A:G
Gene:: PTP4A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.31919018A>G, NC_000001.10:g.32384619A>G, NM_080391.4:c.48T>C, NM_080391.3:c.48T>C, NM_001195100.2:c.48T>C, NM_001195100.1:c.48T>C, NM_001195101.2:c.48T>C, NM_001195101.1:c.48T>C, NM_003479.2:c.48T>C, NM_080392.2:c.48T>C, NM_001369859.1:c.48T>C, NM_001369860.1:c.48T>C, NM_001369858.1:c.48T>C, XM_047431030.1:c.48T>C, XM_047431017.1:c.48T>C, XM_047431024.1:c.48T>C, XM_047431039.1:c.48T>C, XM_047431028.1:c.48T>C, XM_047431032.1:c.48T>C, XM_047431035.1:c.48T>C, NM_080392.1:c.48T>C, NM_003479.1:c.48T>C

Select item 133364176417.

rs1333641764 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:31919000 (GRCh38)
1:32384601 (GRCh37)
Canonical SPDI:: NC_000001.11:31918999:A:G
Gene:: PTP4A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.31919000A>G, NC_000001.10:g.32384601A>G, NM_080391.4:c.66T>C, NM_080391.3:c.66T>C, NM_001195100.2:c.66T>C, NM_001195100.1:c.66T>C, NM_001195101.2:c.66T>C, NM_001195101.1:c.66T>C, NM_003479.2:c.66T>C, NM_080392.2:c.66T>C, NM_001369859.1:c.66T>C, NM_001369860.1:c.66T>C, NM_001369858.1:c.66T>C, XM_047431030.1:c.66T>C, XM_047431017.1:c.66T>C, XM_047431024.1:c.66T>C, XM_047431039.1:c.66T>C, XM_047431028.1:c.66T>C, XM_047431032.1:c.66T>C, XM_047431035.1:c.66T>C, NM_080392.1:c.66T>C, NM_003479.1:c.66T>C

Select item 133145533418.

rs1331455334 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:31915900 (GRCh38)
1:32381501 (GRCh37)
Canonical SPDI:: NC_000001.11:31915899:C:A,NC_000001.11:31915899:C:T
Gene:: PTP4A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.31915900C>A, NC_000001.11:g.31915900C>T, NC_000001.10:g.32381501C>A, NC_000001.10:g.32381501C>T, NM_080391.4:c.184G>T, NM_080391.4:c.184G>A, NM_080391.3:c.184G>T, NM_080391.3:c.184G>A, NM_001195100.2:c.184G>T, NM_001195100.2:c.184G>A, NM_001195100.1:c.184G>T, NM_001195100.1:c.184G>A, NM_003479.2:c.184G>T, NM_003479.2:c.184G>A, NM_080392.2:c.184G>T, NM_080392.2:c.184G>A, NM_001369859.1:c.184G>T, NM_001369859.1:c.184G>A, NM_001369860.1:c.184G>T, NM_001369860.1:c.184G>A, XM_047431030.1:c.184G>T, XM_047431030.1:c.184G>A, XM_047431017.1:c.184G>T, XM_047431017.1:c.184G>A, XM_047431024.1:c.184G>T, XM_047431024.1:c.184G>A, XM_047431028.1:c.184G>T, XM_047431028.1:c.184G>A, XM_047431032.1:c.184G>T, XM_047431032.1:c.184G>A, NM_080392.1:c.184G>T, NM_080392.1:c.184G>A, NM_003479.1:c.184G>T, NM_003479.1:c.184G>A, NP_536316.1:p.Val62Phe, NP_536316.1:p.Val62Ile, NP_001182029.1:p.Val62Phe, NP_001182029.1:p.Val62Ile, NP_001356788.1:p.Val62Phe, NP_001356788.1:p.Val62Ile, NP_001356789.1:p.Val62Phe, NP_001356789.1:p.Val62Ile, XP_047286986.1:p.Val62Phe, XP_047286986.1:p.Val62Ile, XP_047286973.1:p.Val62Phe, XP_047286973.1:p.Val62Ile, XP_047286980.1:p.Val62Phe, XP_047286980.1:p.Val62Ile, XP_047286984.1:p.Val62Phe, XP_047286984.1:p.Val62Ile, XP_047286988.1:p.Val62Phe, XP_047286988.1:p.Val62Ile

Select item 133124265619.

rs1331242656 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:31911786 (GRCh38)
1:32377387 (GRCh37)
Canonical SPDI:: NC_000001.11:31911785:A:G
Gene:: PTP4A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.31911786A>G, NC_000001.10:g.32377387A>G, NM_080391.4:c.230T>C, NM_080391.3:c.230T>C, NM_001195100.2:c.230T>C, NM_001195100.1:c.230T>C, NM_001195101.2:c.137T>C, NM_001195101.1:c.137T>C, NM_003479.2:c.230T>C, NM_001369859.1:c.230T>C, NM_001369860.1:c.230T>C, NM_001369858.1:c.137T>C, XM_047431030.1:c.230T>C, XM_047431017.1:c.230T>C, XM_047431024.1:c.230T>C, XM_047431039.1:c.137T>C, XM_047431028.1:c.230T>C, XM_047431032.1:c.230T>C, XM_047431035.1:c.137T>C, NM_003479.1:c.230T>C, NP_536316.1:p.Ile77Thr, NP_001182029.1:p.Ile77Thr, NP_001182030.1:p.Ile46Thr, NP_001356788.1:p.Ile77Thr, NP_001356789.1:p.Ile77Thr, NP_001356787.1:p.Ile46Thr, XP_047286986.1:p.Ile77Thr, XP_047286973.1:p.Ile77Thr, XP_047286980.1:p.Ile77Thr, XP_047286995.1:p.Ile46Thr, XP_047286984.1:p.Ile77Thr, XP_047286988.1:p.Ile77Thr, XP_047286991.1:p.Ile46Thr

Select item 131317114120.

rs1313171141 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:31908927 (GRCh38)
1:32374528 (GRCh37)
Canonical SPDI:: NC_000001.11:31908926:C:T
Gene:: PTP4A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000001.11:g.31908927C>T, NC_000001.10:g.32374528C>T, NM_080391.4:c.429G>A, NM_080391.3:c.429G>A, NM_001195100.2:c.354G>A, NM_001195100.1:c.354G>A, NM_001195101.2:c.336G>A, NM_001195101.1:c.336G>A, NM_003479.2:c.429G>A, NM_080392.2:c.223G>A, NM_001369859.1:c.429G>A, NM_001369860.1:c.429G>A, NM_001369858.1:c.336G>A, XM_047431030.1:c.429G>A, XM_047431017.1:c.429G>A, XM_047431024.1:c.429G>A, XM_047431039.1:c.336G>A, XM_047431028.1:c.429G>A, XM_047431032.1:c.354G>A, XM_047431035.1:c.336G>A, NM_080392.1:c.223G>A, NM_003479.1:c.429G>A

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Result Filters

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Items: 1 to 20 of 99

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