SNP Links for Protein (Select 6912328) - SNP

Links from Protein

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Select item 14890975031.

rs1489097503 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:85321557 (GRCh38)
1:85787240 (GRCh37)
Canonical SPDI:: NC_000001.11:85321556:T:C
Gene:: DDAH1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.85321557T>C, NC_000001.10:g.85787240T>C, NM_012137.4:c.753A>G, NM_012137.3:c.753A>G, XM_005270710.3:c.444A>G, XM_005270710.2:c.444A>G, XM_005270710.1:c.444A>G, XM_005270707.3:c.468A>G, XM_005270707.2:c.468A>G, XM_005270707.1:c.468A>G, NM_001134445.2:c.444A>G, NM_001134445.1:c.444A>G, XM_011541158.2:c.453A>G, XM_011541158.1:c.453A>G, NM_001330655.2:c.453A>G, NM_001330655.1:c.453A>G, XM_017000889.2:c.474A>G, XM_017000889.1:c.474A>G, XM_047416630.1:c.453A>G

Select item 14884844012.

rs1488484401 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:85464773 (GRCh38)
1:85930456 (GRCh37)
Canonical SPDI:: NC_000001.11:85464772:G:T
Gene:: DDAH1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,coding_sequence_variant,synonymous_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.85464773G>T, NC_000001.10:g.85930456G>T, NM_012137.4:c.273C>A, NM_012137.3:c.273C>A

Select item 14857565903.

rs1485756590 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:85464990 (GRCh38)
1:85930673 (GRCh37)
Canonical SPDI:: NC_000001.11:85464989:C:A
Gene:: DDAH1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,coding_sequence_variant,missense_variant,genic_upstream_transcript_variant
HGVS:: NC_000001.11:g.85464990C>A, NC_000001.10:g.85930673C>A, NM_012137.4:c.56G>T, NM_012137.3:c.56G>T, NP_036269.1:p.Arg19Leu

Select item 14853438414.

rs1485343841 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:85464785 (GRCh38)
1:85930468 (GRCh37)
Canonical SPDI:: NC_000001.11:85464784:C:A
Gene:: DDAH1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,coding_sequence_variant,synonymous_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.85464785C>A, NC_000001.10:g.85930468C>A, NM_012137.4:c.261G>T, NM_012137.3:c.261G>T

Select item 14818325495.

rs1481832549 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:85321567 (GRCh38)
1:85787250 (GRCh37)
Canonical SPDI:: NC_000001.11:85321566:A:G
Gene:: DDAH1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.85321567A>G, NC_000001.10:g.85787250A>G, NM_012137.4:c.743T>C, NM_012137.3:c.743T>C, XM_005270710.3:c.434T>C, XM_005270710.2:c.434T>C, XM_005270710.1:c.434T>C, XM_005270707.3:c.458T>C, XM_005270707.2:c.458T>C, XM_005270707.1:c.458T>C, NM_001134445.2:c.434T>C, NM_001134445.1:c.434T>C, XM_011541158.2:c.443T>C, XM_011541158.1:c.443T>C, NM_001330655.2:c.443T>C, NM_001330655.1:c.443T>C, XM_017000889.2:c.464T>C, XM_017000889.1:c.464T>C, XM_047416630.1:c.443T>C, NP_036269.1:p.Val248Ala, XP_005270767.1:p.Val145Ala, XP_005270764.1:p.Val153Ala, NP_001127917.1:p.Val145Ala, XP_011539460.1:p.Val148Ala, NP_001317584.1:p.Val148Ala, XP_016856378.1:p.Val155Ala, XP_047272586.1:p.Val148Ala

Select item 14812499996.

rs1481249999 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:85350454 (GRCh38)
1:85816137 (GRCh37)
Canonical SPDI:: NC_000001.11:85350453:G:A,NC_000001.11:85350453:G:T
Gene:: DDAH1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.85350454G>A, NC_000001.11:g.85350454G>T, NC_000001.10:g.85816137G>A, NC_000001.10:g.85816137G>T, NM_012137.4:c.558C>T, NM_012137.4:c.558C>A, NM_012137.3:c.558C>T, NM_012137.3:c.558C>A, XM_005270710.3:c.249C>T, XM_005270710.3:c.249C>A, XM_005270710.2:c.249C>T, XM_005270710.2:c.249C>A, XM_005270710.1:c.249C>T, XM_005270710.1:c.249C>A, XM_005270707.3:c.273C>T, XM_005270707.3:c.273C>A, XM_005270707.2:c.273C>T, XM_005270707.2:c.273C>A, XM_005270707.1:c.273C>T, XM_005270707.1:c.273C>A, NM_001134445.2:c.249C>T, NM_001134445.2:c.249C>A, NM_001134445.1:c.249C>T, NM_001134445.1:c.249C>A, XM_011541158.2:c.258C>T, XM_011541158.2:c.258C>A, XM_011541158.1:c.258C>T, XM_011541158.1:c.258C>A, NM_001330655.2:c.258C>T, NM_001330655.2:c.258C>A, NM_001330655.1:c.258C>T, NM_001330655.1:c.258C>A, XM_017000889.2:c.279C>T, XM_017000889.2:c.279C>A, XM_017000889.1:c.279C>T, XM_017000889.1:c.279C>A, XM_047416630.1:c.258C>T, XM_047416630.1:c.258C>A

Select item 14791962497.

rs1479196249 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:85464802 (GRCh38)
1:85930485 (GRCh37)
Canonical SPDI:: NC_000001.11:85464801:C:T
Gene:: DDAH1 (Varview)
Functional Consequence:: missense_variant,intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.85464802C>T, NC_000001.10:g.85930485C>T, NM_012137.4:c.244G>A, NM_012137.3:c.244G>A, NP_036269.1:p.Val82Met

Select item 14739304688.

rs1473930468 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 1:85321540 (GRCh38)
1:85787223 (GRCh37)
Canonical SPDI:: NC_000001.11:85321539:A:G,NC_000001.11:85321539:A:T
Gene:: DDAH1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.85321540A>G, NC_000001.11:g.85321540A>T, NC_000001.10:g.85787223A>G, NC_000001.10:g.85787223A>T, NM_012137.4:c.770T>C, NM_012137.4:c.770T>A, NM_012137.3:c.770T>C, NM_012137.3:c.770T>A, XM_005270710.3:c.461T>C, XM_005270710.3:c.461T>A, XM_005270710.2:c.461T>C, XM_005270710.2:c.461T>A, XM_005270710.1:c.461T>C, XM_005270710.1:c.461T>A, XM_005270707.3:c.485T>C, XM_005270707.3:c.485T>A, XM_005270707.2:c.485T>C, XM_005270707.2:c.485T>A, XM_005270707.1:c.485T>C, XM_005270707.1:c.485T>A, NM_001134445.2:c.461T>C, NM_001134445.2:c.461T>A, NM_001134445.1:c.461T>C, NM_001134445.1:c.461T>A, XM_011541158.2:c.470T>C, XM_011541158.2:c.470T>A, XM_011541158.1:c.470T>C, XM_011541158.1:c.470T>A, NM_001330655.2:c.470T>C, NM_001330655.2:c.470T>A, NM_001330655.1:c.470T>C, NM_001330655.1:c.470T>A, XM_017000889.2:c.491T>C, XM_017000889.2:c.491T>A, XM_017000889.1:c.491T>C, XM_017000889.1:c.491T>A, XM_047416630.1:c.470T>C, XM_047416630.1:c.470T>A, NP_036269.1:p.Leu257Pro, NP_036269.1:p.Leu257Gln, XP_005270767.1:p.Leu154Pro, XP_005270767.1:p.Leu154Gln, XP_005270764.1:p.Leu162Pro, XP_005270764.1:p.Leu162Gln, NP_001127917.1:p.Leu154Pro, NP_001127917.1:p.Leu154Gln, XP_011539460.1:p.Leu157Pro, XP_011539460.1:p.Leu157Gln, NP_001317584.1:p.Leu157Pro, NP_001317584.1:p.Leu157Gln, XP_016856378.1:p.Leu164Pro, XP_016856378.1:p.Leu164Gln, XP_047272586.1:p.Leu157Pro, XP_047272586.1:p.Leu157Gln

Select item 14736571709.

rs1473657170 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:85465009 (GRCh38)
1:85930692 (GRCh37)
Canonical SPDI:: NC_000001.11:85465008:C:T
Gene:: DDAH1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,coding_sequence_variant,upstream_transcript_variant,missense_variant,intron_variant
HGVS:: NC_000001.11:g.85465009C>T, NC_000001.10:g.85930692C>T, NM_012137.4:c.37G>A, NM_012137.3:c.37G>A, NP_036269.1:p.Ala13Thr

Select item 147360236010.

rs1473602360 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:85358774 (GRCh38)
1:85824457 (GRCh37)
Canonical SPDI:: NC_000001.11:85358773:A:G
Gene:: DDAH1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.85358774A>G, NC_000001.10:g.85824457A>G, NM_012137.4:c.377T>C, NM_012137.3:c.377T>C, XM_005270710.3:c.68T>C, XM_005270710.2:c.68T>C, XM_005270710.1:c.68T>C, XM_005270707.3:c.92T>C, XM_005270707.2:c.92T>C, XM_005270707.1:c.92T>C, NM_001134445.2:c.68T>C, NM_001134445.1:c.68T>C, XM_011541158.2:c.77T>C, XM_011541158.1:c.77T>C, NM_001330655.2:c.77T>C, NM_001330655.1:c.77T>C, XM_017000889.2:c.98T>C, XM_017000889.1:c.98T>C, XM_047416630.1:c.77T>C, NP_036269.1:p.Leu126Ser, XP_005270767.1:p.Leu23Ser, XP_005270764.1:p.Leu31Ser, NP_001127917.1:p.Leu23Ser, XP_011539460.1:p.Leu26Ser, NP_001317584.1:p.Leu26Ser, XP_016856378.1:p.Leu33Ser, XP_047272586.1:p.Leu26Ser

Select item 147186673011.

rs1471866730 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:85464938 (GRCh38)
1:85930621 (GRCh37)
Canonical SPDI:: NC_000001.11:85464937:C:G,NC_000001.11:85464937:C:T
Gene:: DDAH1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,synonymous_variant,coding_sequence_variant,upstream_transcript_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0.000007/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.85464938C>G, NC_000001.11:g.85464938C>T, NC_000001.10:g.85930621C>G, NC_000001.10:g.85930621C>T, NM_012137.4:c.108G>C, NM_012137.4:c.108G>A, NM_012137.3:c.108G>C, NM_012137.3:c.108G>A, NP_036269.1:p.Glu36Asp

Select item 147136574112.

rs1471365741 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:85464752 (GRCh38)
1:85930435 (GRCh37)
Canonical SPDI:: NC_000001.11:85464751:C:G
Gene:: DDAH1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,synonymous_variant,coding_sequence_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.85464752C>G, NC_000001.10:g.85930435C>G, NM_012137.4:c.294G>C, NM_012137.3:c.294G>C

Select item 146689119713.

rs1466891197 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:85464959 (GRCh38)
1:85930642 (GRCh37)
Canonical SPDI:: NC_000001.11:85464958:C:A
Gene:: DDAH1 (Varview)
Functional Consequence:: upstream_transcript_variant,synonymous_variant,genic_upstream_transcript_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.85464959C>A, NC_000001.10:g.85930642C>A, NM_012137.4:c.87G>T, NM_012137.3:c.87G>T

Select item 146327172914.

rs1463271729 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:85464905 (GRCh38)
1:85930588 (GRCh37)
Canonical SPDI:: NC_000001.11:85464904:G:A
Gene:: DDAH1 (Varview)
Functional Consequence:: upstream_transcript_variant,synonymous_variant,genic_upstream_transcript_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.85464905G>A, NC_000001.10:g.85930588G>A, NM_012137.4:c.141C>T, NM_012137.3:c.141C>T

Select item 146264145615.

rs1462641456 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TTCATCT [Show Flanks]
Chromosome:: 1:85358783 (GRCh38)
1:85824467 (GRCh37)
Canonical SPDI:: NC_000001.11:85358783:TTTCATCTTTCATCT:TTTCATCTTTCATCTTTCATCT
Gene:: DDAH1 (Varview)
Functional Consequence:: inframe_indel,coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: TTTCATCTTTCATCTTTCATCT=0./0 (ALFA)
TTTCATC=0.000004/1 (TOPMED)
TTTCATC=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.85358785TTCATCT[3], NC_000001.10:g.85824468TTCATCT[3], NM_012137.4:c.361_367dup, NM_012137.3:c.361_367dup, XM_005270710.3:c.52_58dup, XM_005270710.2:c.52_58dup, XM_005270710.1:c.52_58dup, XM_005270707.3:c.76_82dup, XM_005270707.2:c.76_82dup, XM_005270707.1:c.76_82dup, NM_001134445.2:c.52_58dup, NM_001134445.1:c.52_58dup, XM_011541158.2:c.61_67dup, XM_011541158.1:c.61_67dup, NM_001330655.2:c.61_67dup, NM_001330655.1:c.61_67dup, XM_017000889.2:c.82_88dup, XM_017000889.1:c.82_88dup, XM_047416630.1:c.61_67dup, NP_036269.1:p.Asn123delinsArgTer, XP_005270767.1:p.Asn20delinsArgTer, XP_005270764.1:p.Asn28delinsArgTer, NP_001127917.1:p.Asn20delinsArgTer, XP_011539460.1:p.Asn23delinsArgTer, NP_001317584.1:p.Asn23delinsArgTer, XP_016856378.1:p.Asn30delinsArgTer, XP_047272586.1:p.Asn23delinsArgTer

Select item 146239176816.

rs1462391768 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 1:85464924 (GRCh38)
1:85930607 (GRCh37)
Canonical SPDI:: NC_000001.11:85464923:G:C,NC_000001.11:85464923:G:T
Gene:: DDAH1 (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,genic_upstream_transcript_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.85464924G>C, NC_000001.11:g.85464924G>T, NC_000001.10:g.85930607G>C, NC_000001.10:g.85930607G>T, NM_012137.4:c.122C>G, NM_012137.4:c.122C>A, NM_012137.3:c.122C>G, NM_012137.3:c.122C>A, NP_036269.1:p.Ala41Gly, NP_036269.1:p.Ala41Asp

Select item 146022537217.

rs1460225372 [Homo sapiens]

Variant type:: DELINS
Alleles:: TCTT>- [Show Flanks]
Chromosome:: 1:85321466 (GRCh38)
1:85787149 (GRCh37)
Canonical SPDI:: NC_000001.11:85321462:CTTTCTT:CTT
Gene:: DDAH1 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.85321466_85321469del, NC_000001.10:g.85787149_85787152del, NM_012137.4:c.844_847del, NM_012137.3:c.844_847del, XM_005270710.3:c.535_538del, XM_005270710.2:c.535_538del, XM_005270710.1:c.535_538del, XM_005270707.3:c.559_562del, XM_005270707.2:c.559_562del, XM_005270707.1:c.559_562del, NM_001134445.2:c.535_538del, NM_001134445.1:c.535_538del, XM_011541158.2:c.544_547del, XM_011541158.1:c.544_547del, NM_001330655.2:c.544_547del, NM_001330655.1:c.544_547del, XM_017000889.2:c.565_568del, XM_017000889.1:c.565_568del, XM_047416630.1:c.544_547del, NP_036269.1:p.Lys281_Lys282insTer, XP_005270767.1:p.Lys178_Lys179insTer, XP_005270764.1:p.Lys186_Lys187insTer, NP_001127917.1:p.Lys178_Lys179insTer, XP_011539460.1:p.Lys181_Lys182insTer, NP_001317584.1:p.Lys181_Lys182insTer, XP_016856378.1:p.Lys188_Lys189insTer, XP_047272586.1:p.Lys181_Lys182insTer

Select item 145284033618.

rs1452840336 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:85465020 (GRCh38)
1:85930703 (GRCh37)
Canonical SPDI:: NC_000001.11:85465019:G:A,NC_000001.11:85465019:G:C
Gene:: DDAH1 (Varview)
Functional Consequence:: coding_sequence_variant,upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.85465020G>A, NC_000001.11:g.85465020G>C, NC_000001.10:g.85930703G>A, NC_000001.10:g.85930703G>C, NM_012137.4:c.26C>T, NM_012137.4:c.26C>G, NM_012137.3:c.26C>T, NM_012137.3:c.26C>G, NP_036269.1:p.Ala9Val, NP_036269.1:p.Ala9Gly

Select item 145183429519.

rs1451834295 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:85464808 (GRCh38)
1:85930491 (GRCh37)
Canonical SPDI:: NC_000001.11:85464807:C:T
Gene:: DDAH1 (Varview)
Functional Consequence:: coding_sequence_variant,upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.85464808C>T, NC_000001.10:g.85930491C>T, NM_012137.4:c.238G>A, NM_012137.3:c.238G>A, NP_036269.1:p.Val80Met

Select item 144074685520.

rs1440746855 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:85465003 (GRCh38)
1:85930686 (GRCh37)
Canonical SPDI:: NC_000001.11:85465002:G:A
Gene:: DDAH1 (Varview)
Functional Consequence:: missense_variant,genic_upstream_transcript_variant,intron_variant,coding_sequence_variant,upstream_transcript_variant
HGVS:: NC_000001.11:g.85465003G>A, NC_000001.10:g.85930686G>A, NM_012137.4:c.43C>T, NM_012137.3:c.43C>T, NP_036269.1:p.His15Tyr

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