SNP Links for Protein (Select 662033864) - SNP

Links from Protein

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Select item 14908226781.

rs1490822678 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:13663042 (GRCh38)
X:13681161 (GRCh37)
Canonical SPDI:: NC_000023.11:13663041:A:G
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000006/1 (GnomAD_exomes)
G=0.00001/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.13663042A>G, NC_000023.10:g.13681161A>G, NM_152634.4:c.624A>G, NM_152634.3:c.624A>G, NM_152634.2:c.624A>G, NM_001297563.2:c.534A>G, NM_001297563.1:c.534A>G, XM_017029316.2:c.624A>G, XM_017029316.1:c.624A>G, NM_001297564.2:c.534A>G, NM_001297564.1:c.534A>G, NP_689847.2:p.Ile208Met, NP_001284492.1:p.Ile178Met, XP_016884805.1:p.Ile208Met, NP_001284493.1:p.Ile178Met

Select item 14882530582.

rs1488253058 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:13662600 (GRCh38)
X:13680719 (GRCh37)
Canonical SPDI:: NC_000023.11:13662599:C:T
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000022/4 (GnomAD_exomes)
HGVS:: NC_000023.11:g.13662600C>T, NC_000023.10:g.13680719C>T, NM_152634.4:c.182C>T, NM_152634.3:c.182C>T, NM_152634.2:c.182C>T, NM_001297563.2:c.92C>T, NM_001297563.1:c.92C>T, XM_017029316.2:c.182C>T, XM_017029316.1:c.182C>T, NM_001297564.2:c.92C>T, NM_001297564.1:c.92C>T, NP_689847.2:p.Thr61Ile, NP_001284492.1:p.Thr31Ile, XP_016884805.1:p.Thr61Ile, NP_001284493.1:p.Thr31Ile

Select item 14872869783.

rs1487286978 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:13662571 (GRCh38)
X:13680690 (GRCh37)
Canonical SPDI:: NC_000023.11:13662570:G:T
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.13662571G>T, NC_000023.10:g.13680690G>T, NM_152634.4:c.153G>T, NM_152634.3:c.153G>T, NM_152634.2:c.153G>T, NM_001297563.2:c.63G>T, NM_001297563.1:c.63G>T, XM_017029316.2:c.153G>T, XM_017029316.1:c.153G>T, NM_001297564.2:c.63G>T, NM_001297564.1:c.63G>T, NP_689847.2:p.Arg51Ser, NP_001284492.1:p.Arg21Ser, XP_016884805.1:p.Arg51Ser, NP_001284493.1:p.Arg21Ser

Select item 14864683804.

rs1486468380 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: X:13662730 (GRCh38)
X:13680849 (GRCh37)
Canonical SPDI:: NC_000023.11:13662729:G:A,NC_000023.11:13662729:G:T
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
HGVS:: NC_000023.11:g.13662730G>A, NC_000023.11:g.13662730G>T, NC_000023.10:g.13680849G>A, NC_000023.10:g.13680849G>T, NM_152634.4:c.312G>A, NM_152634.4:c.312G>T, NM_152634.3:c.312G>A, NM_152634.3:c.312G>T, NM_152634.2:c.312G>A, NM_152634.2:c.312G>T, NM_001297563.2:c.222G>A, NM_001297563.2:c.222G>T, NM_001297563.1:c.222G>A, NM_001297563.1:c.222G>T, XM_017029316.2:c.312G>A, XM_017029316.2:c.312G>T, XM_017029316.1:c.312G>A, XM_017029316.1:c.312G>T, NM_001297564.2:c.222G>A, NM_001297564.2:c.222G>T, NM_001297564.1:c.222G>A, NM_001297564.1:c.222G>T, NP_689847.2:p.Lys104Asn, NP_001284492.1:p.Lys74Asn, XP_016884805.1:p.Lys104Asn, NP_001284493.1:p.Lys74Asn

Select item 14810443485.

rs1481044348 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:13663105 (GRCh38)
X:13681224 (GRCh37)
Canonical SPDI:: NC_000023.11:13663104:A:G
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.13663105A>G, NC_000023.10:g.13681224A>G, NM_152634.4:c.687A>G, NM_152634.3:c.687A>G, NM_152634.2:c.687A>G, NM_001297563.2:c.597A>G, NM_001297563.1:c.597A>G, XM_017029316.2:c.687A>G, XM_017029316.1:c.687A>G, NM_001297564.2:c.597A>G, NM_001297564.1:c.597A>G

Select item 14797385226.

rs1479738522 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:13663445 (GRCh38)
X:13681564 (GRCh37)
Canonical SPDI:: NC_000023.11:13663444:G:A
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.13663445G>A, NC_000023.10:g.13681564G>A, NM_152634.4:c.1027G>A, NM_152634.3:c.1027G>A, NM_152634.2:c.1027G>A, NM_001297563.2:c.937G>A, NM_001297563.1:c.937G>A, XM_017029316.2:c.1027G>A, XM_017029316.1:c.1027G>A, NM_001297564.2:c.937G>A, NM_001297564.1:c.937G>A, NP_689847.2:p.Gly343Arg, NP_001284492.1:p.Gly313Arg, XP_016884805.1:p.Gly343Arg, NP_001284493.1:p.Gly313Arg

Select item 14706937437.

rs1470693743 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:13662892 (GRCh38)
X:13681011 (GRCh37)
Canonical SPDI:: NC_000023.11:13662891:T:C
Gene:: TCEANC (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000006/1 (GnomAD_exomes)
C=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.13662892T>C, NC_000023.10:g.13681011T>C, NM_152634.4:c.474T>C, NM_152634.3:c.474T>C, NM_152634.2:c.474T>C, NM_001297563.2:c.384T>C, NM_001297563.1:c.384T>C, XM_017029316.2:c.474T>C, XM_017029316.1:c.474T>C, NM_001297564.2:c.384T>C, NM_001297564.1:c.384T>C

Select item 14653480518.

rs1465348051 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:13663472 (GRCh38)
X:13681591 (GRCh37)
Canonical SPDI:: NC_000023.11:13663471:C:T
Gene:: TCEANC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000023.11:g.13663472C>T, NC_000023.10:g.13681591C>T, NM_152634.4:c.1054C>T, NM_152634.3:c.1054C>T, NM_152634.2:c.1054C>T, NM_001297563.2:c.964C>T, NM_001297563.1:c.964C>T, XM_017029316.2:c.1054C>T, XM_017029316.1:c.1054C>T, NM_001297564.2:c.964C>T, NM_001297564.1:c.964C>T, NP_689847.2:p.Arg352Trp, NP_001284492.1:p.Arg322Trp, XP_016884805.1:p.Arg352Trp, NP_001284493.1:p.Arg322Trp

Select item 14542670169.

rs1454267016 [Homo sapiens]

Variant type:: INS
Alleles:: ->CA [Show Flanks]
Chromosome:: X:13662790 (GRCh38)
X:13680910 (GRCh37)
Canonical SPDI:: NC_000023.11:13662790::CA
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
HGVS:: NC_000023.11:g.13662790_13662791insCA, NC_000023.10:g.13680909_13680910insCA, NM_152634.4:c.372_373insCA, NM_152634.3:c.372_373insCA, NM_152634.2:c.372_373insCA, NM_001297563.2:c.282_283insCA, NM_001297563.1:c.282_283insCA, XM_017029316.2:c.372_373insCA, XM_017029316.1:c.372_373insCA, NM_001297564.2:c.282_283insCA, NM_001297564.1:c.282_283insCA, NP_689847.2:p.Val125fs, NP_001284492.1:p.Val95fs, XP_016884805.1:p.Val125fs, NP_001284493.1:p.Val95fs

Select item 145324228110.

rs1453242281 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:13662973 (GRCh38)
X:13681092 (GRCh37)
Canonical SPDI:: NC_000023.11:13662972:C:T
Gene:: TCEANC (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=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.13662973C>T, NC_000023.10:g.13681092C>T, NM_152634.4:c.555C>T, NM_152634.3:c.555C>T, NM_152634.2:c.555C>T, NM_001297563.2:c.465C>T, NM_001297563.1:c.465C>T, XM_017029316.2:c.555C>T, XM_017029316.1:c.555C>T, NM_001297564.2:c.465C>T, NM_001297564.1:c.465C>T

Select item 144623026111.

rs1446230261 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:13663370 (GRCh38)
X:13681489 (GRCh37)
Canonical SPDI:: NC_000023.11:13663369:G:T
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000026/7 (TOPMED)
HGVS:: NC_000023.11:g.13663370G>T, NC_000023.10:g.13681489G>T, NM_152634.4:c.952G>T, NM_152634.3:c.952G>T, NM_152634.2:c.952G>T, NM_001297563.2:c.862G>T, NM_001297563.1:c.862G>T, XM_017029316.2:c.952G>T, XM_017029316.1:c.952G>T, NM_001297564.2:c.862G>T, NM_001297564.1:c.862G>T, NP_689847.2:p.Asp318Tyr, NP_001284492.1:p.Asp288Tyr, XP_016884805.1:p.Asp318Tyr, NP_001284493.1:p.Asp288Tyr

Select item 144519405112.

rs1445194051 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:13663207 (GRCh38)
X:13681326 (GRCh37)
Canonical SPDI:: NC_000023.11:13663206:C:T
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.13663207C>T, NC_000023.10:g.13681326C>T, NM_152634.4:c.789C>T, NM_152634.3:c.789C>T, NM_152634.2:c.789C>T, NM_001297563.2:c.699C>T, NM_001297563.1:c.699C>T, XM_017029316.2:c.789C>T, XM_017029316.1:c.789C>T, NM_001297564.2:c.699C>T, NM_001297564.1:c.699C>T

Select item 144412406313.

rs1444124063 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:13662903 (GRCh38)
X:13681022 (GRCh37)
Canonical SPDI:: NC_000023.11:13662902:G:A
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000011/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.13662903G>A, NC_000023.10:g.13681022G>A, NM_152634.4:c.485G>A, NM_152634.3:c.485G>A, NM_152634.2:c.485G>A, NM_001297563.2:c.395G>A, NM_001297563.1:c.395G>A, XM_017029316.2:c.485G>A, XM_017029316.1:c.485G>A, NM_001297564.2:c.395G>A, NM_001297564.1:c.395G>A, NP_689847.2:p.Ser162Asn, NP_001284492.1:p.Ser132Asn, XP_016884805.1:p.Ser162Asn, NP_001284493.1:p.Ser132Asn

Select item 144129435714.

rs1441294357 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:13663307 (GRCh38)
X:13681426 (GRCh37)
Canonical SPDI:: NC_000023.11:13663306:A:C
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.13663307A>C, NC_000023.10:g.13681426A>C, NM_152634.4:c.889A>C, NM_152634.3:c.889A>C, NM_152634.2:c.889A>C, NM_001297563.2:c.799A>C, NM_001297563.1:c.799A>C, XM_017029316.2:c.889A>C, XM_017029316.1:c.889A>C, NM_001297564.2:c.799A>C, NM_001297564.1:c.799A>C, NP_689847.2:p.Lys297Gln, NP_001284492.1:p.Lys267Gln, XP_016884805.1:p.Lys297Gln, NP_001284493.1:p.Lys267Gln

Select item 143804806015.

rs1438048060 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:13662850 (GRCh38)
X:13680969 (GRCh37)
Canonical SPDI:: NC_000023.11:13662849:A:G
Gene:: TCEANC (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000006/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.13662850A>G, NC_000023.10:g.13680969A>G, NM_152634.4:c.432A>G, NM_152634.3:c.432A>G, NM_152634.2:c.432A>G, NM_001297563.2:c.342A>G, NM_001297563.1:c.342A>G, XM_017029316.2:c.432A>G, XM_017029316.1:c.432A>G, NM_001297564.2:c.342A>G, NM_001297564.1:c.342A>G

Select item 143469362616.

rs1434693626 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:13663484 (GRCh38)
X:13681603 (GRCh37)
Canonical SPDI:: NC_000023.11:13663483:C:G
Gene:: TCEANC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00003/8 (TOPMED)
G=0.000038/4 (GnomAD)
HGVS:: NC_000023.11:g.13663484C>G, NC_000023.10:g.13681603C>G, NM_152634.4:c.1066C>G, NM_152634.3:c.1066C>G, NM_152634.2:c.1066C>G, NM_001297563.2:c.976C>G, NM_001297563.1:c.976C>G, XM_017029316.2:c.1066C>G, XM_017029316.1:c.1066C>G, NM_001297564.2:c.976C>G, NM_001297564.1:c.976C>G, NP_689847.2:p.Pro356Ala, NP_001284492.1:p.Pro326Ala, XP_016884805.1:p.Pro356Ala, NP_001284493.1:p.Pro326Ala

Select item 143277358517.

rs1432773585 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:13662871 (GRCh38)
X:13680990 (GRCh37)
Canonical SPDI:: NC_000023.11:13662870:T:A
Gene:: TCEANC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.13662871T>A, NC_000023.10:g.13680990T>A, NM_152634.4:c.453T>A, NM_152634.3:c.453T>A, NM_152634.2:c.453T>A, NM_001297563.2:c.363T>A, NM_001297563.1:c.363T>A, XM_017029316.2:c.453T>A, XM_017029316.1:c.453T>A, NM_001297564.2:c.363T>A, NM_001297564.1:c.363T>A, NP_689847.2:p.Asn151Lys, NP_001284492.1:p.Asn121Lys, XP_016884805.1:p.Asn151Lys, NP_001284493.1:p.Asn121Lys

Select item 143192998418.

rs1431929984 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:13662533 (GRCh38)
X:13680652 (GRCh37)
Canonical SPDI:: NC_000023.11:13662532:G:T
Gene:: TCEANC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.13662533G>T, NC_000023.10:g.13680652G>T, NM_152634.4:c.115G>T, NM_152634.3:c.115G>T, NM_152634.2:c.115G>T, NM_001297563.2:c.25G>T, NM_001297563.1:c.25G>T, XM_017029316.2:c.115G>T, XM_017029316.1:c.115G>T, NM_001297564.2:c.25G>T, NM_001297564.1:c.25G>T, NP_689847.2:p.Ala39Ser, NP_001284492.1:p.Ala9Ser, XP_016884805.1:p.Ala39Ser, NP_001284493.1:p.Ala9Ser

Select item 143180102919.

rs1431801029 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:13662690 (GRCh38)
X:13680809 (GRCh37)
Canonical SPDI:: NC_000023.11:13662689:C:G
Gene:: TCEANC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.13662690C>G, NC_000023.10:g.13680809C>G, NM_152634.4:c.272C>G, NM_152634.3:c.272C>G, NM_152634.2:c.272C>G, NM_001297563.2:c.182C>G, NM_001297563.1:c.182C>G, XM_017029316.2:c.272C>G, XM_017029316.1:c.272C>G, NM_001297564.2:c.182C>G, NM_001297564.1:c.182C>G, NP_689847.2:p.Ser91Cys, NP_001284492.1:p.Ser61Cys, XP_016884805.1:p.Ser91Cys, NP_001284493.1:p.Ser61Cys

Select item 142916109220.

rs1429161092 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:13662615 (GRCh38)
X:13680734 (GRCh37)
Canonical SPDI:: NC_000023.11:13662614:T:G
Gene:: TCEANC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.13662615T>G, NC_000023.10:g.13680734T>G, NM_152634.4:c.197T>G, NM_152634.3:c.197T>G, NM_152634.2:c.197T>G, NM_001297563.2:c.107T>G, NM_001297563.1:c.107T>G, XM_017029316.2:c.197T>G, XM_017029316.1:c.197T>G, NM_001297564.2:c.107T>G, NM_001297564.1:c.107T>G, NP_689847.2:p.Ile66Ser, NP_001284492.1:p.Ile36Ser, XP_016884805.1:p.Ile66Ser, NP_001284493.1:p.Ile36Ser

dbSNP

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