SNP Links for Protein (Select 170172518) - SNP

Links from Protein

Items: 1 to 20 of 930

<< First< Prev

Page of 47

Next >Last >>

Select item 14907547301.

rs1490754730 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 22:17896329 (GRCh38)
22:18379095 (GRCh37)
Canonical SPDI:: NC_000022.11:17896328:C:G
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000111/1 (ALFA)
G=0.000006/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.17896329C>G, NC_000022.10:g.18379095C>G, NM_015241.3:c.1239G>C, NM_015241.2:c.1239G>C, NM_001136004.3:c.1239G>C, NM_001136004.2:c.1239G>C, NM_001136004.1:c.1239G>C, NM_001122731.2:c.1239G>C, NM_001122731.1:c.1239G>C, NM_020793.1:c.1239G>C

Select item 14897312612.

rs1489731261 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 22:17904774 (GRCh38)
22:18387540 (GRCh37)
Canonical SPDI:: NC_000022.11:17904773:G:C
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.17904774G>C, NC_000022.10:g.18387540G>C, NM_015241.3:c.330C>G, NM_015241.2:c.330C>G, NM_001136004.3:c.330C>G, NM_001136004.2:c.330C>G, NM_001136004.1:c.330C>G, NM_001122731.2:c.330C>G, NM_001122731.1:c.330C>G, NM_020793.1:c.330C>G

Select item 14884310273.

rs1488431027 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 22:17834542 (GRCh38)
22:18317308 (GRCh37)
Canonical SPDI:: NC_000022.11:17834541:C:G,NC_000022.11:17834541:C:T
Gene:: MICAL3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.17834542C>G, NC_000022.11:g.17834542C>T, NC_000022.10:g.18317308C>G, NC_000022.10:g.18317308C>T, NM_001122731.2:c.2809G>C, NM_001122731.2:c.2809G>A, NM_001122731.1:c.2809G>C, NM_001122731.1:c.2809G>A, NP_001116203.1:p.Val937Leu, NP_001116203.1:p.Val937Ile

Select item 14854189914.

rs1485418991 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:17842017 (GRCh38)
22:18324783 (GRCh37)
Canonical SPDI:: NC_000022.11:17842016:C:T
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
HGVS:: NC_000022.11:g.17842017C>T, NC_000022.10:g.18324783C>T, NM_015241.3:c.2606G>A, NM_015241.2:c.2606G>A, NM_001122731.2:c.2606G>A, NM_001122731.1:c.2606G>A, NM_020793.1:c.2606G>A, NP_056056.2:p.Gly869Asp, NP_001116203.1:p.Gly869Asp

Select item 14843524825.

rs1484352482 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 22:17885951 (GRCh38)
22:18368717 (GRCh37)
Canonical SPDI:: NC_000022.11:17885950:T:C,NC_000022.11:17885950:T:G
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.17885951T>C, NC_000022.11:g.17885951T>G, NC_000022.10:g.18368717T>C, NC_000022.10:g.18368717T>G, NM_015241.3:c.2168A>G, NM_015241.3:c.2168A>C, NM_015241.2:c.2168A>G, NM_015241.2:c.2168A>C, NM_001136004.3:c.2168A>G, NM_001136004.3:c.2168A>C, NM_001136004.2:c.2168A>G, NM_001136004.2:c.2168A>C, NM_001136004.1:c.2168A>G, NM_001136004.1:c.2168A>C, NM_001122731.2:c.2168A>G, NM_001122731.2:c.2168A>C, NM_001122731.1:c.2168A>G, NM_001122731.1:c.2168A>C, NM_020793.1:c.2168A>G, NM_020793.1:c.2168A>C, NP_056056.2:p.Lys723Arg, NP_056056.2:p.Lys723Thr, NP_001129476.1:p.Lys723Arg, NP_001129476.1:p.Lys723Thr, NP_001116203.1:p.Lys723Arg, NP_001116203.1:p.Lys723Thr

Select item 14840691756.

rs1484069175 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:17906621 (GRCh38)
22:18389387 (GRCh37)
Canonical SPDI:: NC_000022.11:17906620:G:A
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.17906621G>A, NC_000022.10:g.18389387G>A, NM_015241.3:c.192C>T, NM_015241.2:c.192C>T, NM_001136004.3:c.192C>T, NM_001136004.2:c.192C>T, NM_001136004.1:c.192C>T, NM_001122731.2:c.192C>T, NM_001122731.1:c.192C>T, NM_020793.1:c.192C>T

Select item 14839266137.

rs1483926613 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 22:17834544 (GRCh38)
22:18317310 (GRCh37)
Canonical SPDI:: NC_000022.11:17834543:C:G
Gene:: MICAL3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000016/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.17834544C>G, NC_000022.10:g.18317310C>G, NM_001122731.2:c.2807G>C, NM_001122731.1:c.2807G>C, NP_001116203.1:p.Trp936Ser

Select item 14774716148.

rs1477471614 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:17900910 (GRCh38)
22:18383676 (GRCh37)
Canonical SPDI:: NC_000022.11:17900909:A:G
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.17900910A>G, NC_000022.10:g.18383676A>G, NM_015241.3:c.779T>C, NM_015241.2:c.779T>C, NM_001136004.3:c.779T>C, NM_001136004.2:c.779T>C, NM_001136004.1:c.779T>C, NM_001122731.2:c.779T>C, NM_001122731.1:c.779T>C, NM_020793.1:c.779T>C, NP_056056.2:p.Val260Ala, NP_001129476.1:p.Val260Ala, NP_001116203.1:p.Val260Ala

Select item 14768923549.

rs1476892354 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:17841954 (GRCh38)
22:18324720 (GRCh37)
Canonical SPDI:: NC_000022.11:17841953:C:T
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000049/13 (TOPMED)
HGVS:: NC_000022.11:g.17841954C>T, NC_000022.10:g.18324720C>T, NM_015241.3:c.2669G>A, NM_015241.2:c.2669G>A, NM_001122731.2:c.2669G>A, NM_001122731.1:c.2669G>A, NM_020793.1:c.2669G>A, NP_056056.2:p.Arg890Gln, NP_001116203.1:p.Arg890Gln

Select item 147596029210.

rs1475960292 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 22:17900880 (GRCh38)
22:18383646 (GRCh37)
Canonical SPDI:: NC_000022.11:17900879:A:C
Gene:: MICAL3 (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_000022.11:g.17900880A>C, NC_000022.10:g.18383646A>C, NM_015241.3:c.809T>G, NM_015241.2:c.809T>G, NM_001136004.3:c.809T>G, NM_001136004.2:c.809T>G, NM_001136004.1:c.809T>G, NM_001122731.2:c.809T>G, NM_001122731.1:c.809T>G, NM_020793.1:c.809T>G, NP_056056.2:p.Phe270Cys, NP_001129476.1:p.Phe270Cys, NP_001116203.1:p.Phe270Cys

Select item 147436938611.

rs1474369386 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 22:17889050 (GRCh38)
22:18371816 (GRCh37)
Canonical SPDI:: NC_000022.11:17889049:G:C
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.17889050G>C, NC_000022.10:g.18371816G>C, NM_015241.3:c.1875C>G, NM_015241.2:c.1875C>G, NM_001136004.3:c.1875C>G, NM_001136004.2:c.1875C>G, NM_001136004.1:c.1875C>G, NM_001122731.2:c.1875C>G, NM_001122731.1:c.1875C>G, NM_020793.1:c.1875C>G, NP_056056.2:p.Asp625Glu, NP_001129476.1:p.Asp625Glu, NP_001116203.1:p.Asp625Glu

Select item 147089058312.

rs1470890583 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:17904675 (GRCh38)
22:18387441 (GRCh37)
Canonical SPDI:: NC_000022.11:17904674:C:T
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000022.11:g.17904675C>T, NC_000022.10:g.18387441C>T, NM_015241.3:c.429G>A, NM_015241.2:c.429G>A, NM_001136004.3:c.429G>A, NM_001136004.2:c.429G>A, NM_001136004.1:c.429G>A, NM_001122731.2:c.429G>A, NM_001122731.1:c.429G>A, NM_020793.1:c.429G>A

Select item 147021985313.

rs1470219853 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 22:17893847 (GRCh38)
22:18376613 (GRCh37)
Canonical SPDI:: NC_000022.11:17893846:G:A,NC_000022.11:17893846:G:C
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000224/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000223/1 (Estonian)
HGVS:: NC_000022.11:g.17893847G>A, NC_000022.11:g.17893847G>C, NC_000022.10:g.18376613G>A, NC_000022.10:g.18376613G>C, NM_015241.3:c.1507C>T, NM_015241.3:c.1507C>G, NM_015241.2:c.1507C>T, NM_015241.2:c.1507C>G, NM_001136004.3:c.1507C>T, NM_001136004.3:c.1507C>G, NM_001136004.2:c.1507C>T, NM_001136004.2:c.1507C>G, NM_001136004.1:c.1507C>T, NM_001136004.1:c.1507C>G, NM_001122731.2:c.1507C>T, NM_001122731.2:c.1507C>G, NM_001122731.1:c.1507C>T, NM_001122731.1:c.1507C>G, NM_020793.1:c.1507C>T, NM_020793.1:c.1507C>G, NP_056056.2:p.Leu503Val, NP_001129476.1:p.Leu503Val, NP_001116203.1:p.Leu503Val

Select item 146907888814.

rs1469078888 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 22:17864933 (GRCh38)
22:18347699 (GRCh37)
Canonical SPDI:: NC_000022.11:17864932:G:C
Gene:: MICAL3 (Varview), LOC124905075 (Varview)
Functional Consequence:: 2KB_upstream_variant,coding_sequence_variant,upstream_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000056/2 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000022.11:g.17864933G>C, NC_000022.10:g.18347699G>C, NM_015241.3:c.2571C>G, NM_015241.2:c.2571C>G, NM_001136004.3:c.2943C>G, NM_001136004.2:c.2943C>G, NM_001136004.1:c.2943C>G, NM_001122731.2:c.2571C>G, NM_001122731.1:c.2571C>G, NM_020793.1:c.2571C>G

Select item 146811212115.

rs1468112121 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:17865972 (GRCh38)
22:18348738 (GRCh37)
Canonical SPDI:: NC_000022.11:17865971:A:G
Gene:: MICAL3 (Varview), LOC124905075 (Varview)
Functional Consequence:: 2KB_upstream_variant,coding_sequence_variant,upstream_transcript_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.17865972A>G, NC_000022.10:g.18348738A>G, NM_015241.3:c.2469T>C, NM_015241.2:c.2469T>C, NM_001136004.3:c.2841T>C, NM_001136004.2:c.2841T>C, NM_001136004.1:c.2841T>C, NM_001122731.2:c.2469T>C, NM_001122731.1:c.2469T>C, NM_020793.1:c.2469T>C

Select item 146769287716.

rs1467692877 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 22:17906681 (GRCh38)
22:18389447 (GRCh37)
Canonical SPDI:: NC_000022.11:17906680:C:G
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.17906681C>G, NC_000022.10:g.18389447C>G, NM_015241.3:c.132G>C, NM_015241.2:c.132G>C, NM_001136004.3:c.132G>C, NM_001136004.2:c.132G>C, NM_001136004.1:c.132G>C, NM_001122731.2:c.132G>C, NM_001122731.1:c.132G>C, NM_020793.1:c.132G>C, NP_056056.2:p.Lys44Asn, NP_001129476.1:p.Lys44Asn, NP_001116203.1:p.Lys44Asn

Select item 146635326117.

rs1466353261 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:17841932 (GRCh38)
22:18324698 (GRCh37)
Canonical SPDI:: NC_000022.11:17841931:G:A
Gene:: MICAL3 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.17841932G>A, NC_000022.10:g.18324698G>A, NM_015241.3:c.2691C>T, NM_015241.2:c.2691C>T, NM_001122731.2:c.2691C>T, NM_001122731.1:c.2691C>T, NM_020793.1:c.2691C>T

Select item 146577889618.

rs1465778896 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:17901908 (GRCh38)
22:18384674 (GRCh37)
Canonical SPDI:: NC_000022.11:17901907:C:T
Gene:: MICAL3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000022.11:g.17901908C>T, NC_000022.10:g.18384674C>T, NM_015241.3:c.661G>A, NM_015241.2:c.661G>A, NM_001136004.3:c.661G>A, NM_001136004.2:c.661G>A, NM_001136004.1:c.661G>A, NM_001122731.2:c.661G>A, NM_001122731.1:c.661G>A, NM_020793.1:c.661G>A, NP_056056.2:p.Gly221Ser, NP_001129476.1:p.Gly221Ser, NP_001116203.1:p.Gly221Ser

Select item 146507732519.

rs1465077325 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:17834465 (GRCh38)
22:18317231 (GRCh37)
Canonical SPDI:: NC_000022.11:17834464:C:T
Gene:: MICAL3 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000015/2 (GnomAD_exomes)
HGVS:: NC_000022.11:g.17834465C>T, NC_000022.10:g.18317231C>T, NM_001122731.2:c.2886G>A, NM_001122731.1:c.2886G>A

Select item 146502797920.

rs1465027979 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:17896269 (GRCh38)
22:18379035 (GRCh37)
Canonical SPDI:: NC_000022.11:17896268:G:A
Gene:: MICAL3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.17896269G>A, NC_000022.10:g.18379035G>A, NM_015241.3:c.1299C>T, NM_015241.2:c.1299C>T, NM_001136004.3:c.1299C>T, NM_001136004.2:c.1299C>T, NM_001136004.1:c.1299C>T, NM_001122731.2:c.1299C>T, NM_001122731.1:c.1299C>T, NM_020793.1:c.1299C>T

<< First< Prev

Page of 47

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 Protein

Items: 1 to 20 of 930

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity