SNP Links for Protein (Select 401461821) - SNP

Links from Protein

Items: 1 to 20 of 324

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Select item 14860455651.

rs1486045565 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 17:81715069 (GRCh38)
17:79682099 (GRCh37)
Canonical SPDI:: NC_000017.11:81715068:A:T
Gene:: SLC25A10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000017.11:g.81715069A>T, NC_000017.10:g.79682099A>T, NM_012140.5:c.210A>T, NM_012140.4:c.210A>T, NM_001270888.2:c.210A>T, NM_001270888.1:c.210A>T, NM_001270953.2:c.210A>T, NM_001270953.1:c.210A>T, XM_047435432.1:c.81A>T, XM_047435431.1:c.210A>T, NP_036272.2:p.Arg70Ser, NP_001257817.1:p.Arg70Ser, NP_001257882.1:p.Arg70Ser, XP_047291388.1:p.Arg27Ser, XP_047291387.1:p.Arg70Ser

Select item 14860302402.

rs1486030240 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:81720053 (GRCh38)
17:79687083 (GRCh37)
Canonical SPDI:: NC_000017.11:81720052:C:T
Gene:: SLC25A10 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,synonymous_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000111/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.81720053C>T, NC_000017.10:g.79687083C>T, NM_012140.5:c.840C>T, NM_012140.4:c.840C>T, NM_001270888.2:c.867C>T, NM_001270888.1:c.867C>T, NM_001270953.2:c.757C>T, NM_001270953.1:c.757C>T, XM_047435432.1:c.711C>T, NP_001257882.1:p.Leu253Phe

Select item 14816354543.

rs1481635454 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:81717067 (GRCh38)
17:79684097 (GRCh37)
Canonical SPDI:: NC_000017.11:81717066:G:C
Gene:: SLC25A10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.81717067G>C, NC_000017.10:g.79684097G>C, NM_012140.5:c.529G>C, NM_012140.4:c.529G>C, NM_001270888.2:c.529G>C, NM_001270888.1:c.529G>C, NM_001270953.2:c.529G>C, NM_001270953.1:c.529G>C, XM_047435432.1:c.400G>C, XM_047435431.1:c.529G>C, NP_036272.2:p.Gly177Arg, NP_001257817.1:p.Gly177Arg, NP_001257882.1:p.Gly177Arg, XP_047291388.1:p.Gly134Arg, XP_047291387.1:p.Gly177Arg

Select item 14811468874.

rs1481146887 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:81720060 (GRCh38)
17:79687090 (GRCh37)
Canonical SPDI:: NC_000017.11:81720059:A:G
Gene:: SLC25A10 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.81720060A>G, NC_000017.10:g.79687090A>G, NM_012140.5:c.847A>G, NM_012140.4:c.847A>G, NM_001270888.2:c.874A>G, NM_001270888.1:c.874A>G, NM_001270953.2:c.764A>G, NM_001270953.1:c.764A>G, XM_047435432.1:c.718A>G, NP_036272.2:p.Ile283Val, NP_001257817.1:p.Ile292Val, NP_001257882.1:p.His255Arg, XP_047291388.1:p.Ile240Val

Select item 14803657645.

rs1480365764 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:81716030 (GRCh38)
17:79683060 (GRCh37)
Canonical SPDI:: NC_000017.11:81716029:G:C
Gene:: SLC25A10 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000017.11:g.81716030G>C, NC_000017.10:g.79683060G>C, NM_012140.5:c.399G>C, NM_012140.4:c.399G>C, NM_001270888.2:c.399G>C, NM_001270888.1:c.399G>C, NM_001270953.2:c.399G>C, NM_001270953.1:c.399G>C, XM_047435432.1:c.270G>C, XM_047435431.1:c.399G>C

Select item 14745736596.

rs1474573659 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 17:81715490 (GRCh38)
17:79682520 (GRCh37)
Canonical SPDI:: NC_000017.11:81715489:C:G
Gene:: SLC25A10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000014/2 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000017.11:g.81715490C>G, NC_000017.10:g.79682520C>G, NM_012140.5:c.226C>G, NM_012140.4:c.226C>G, NM_001270888.2:c.226C>G, NM_001270888.1:c.226C>G, NM_001270953.2:c.226C>G, NM_001270953.1:c.226C>G, XM_047435432.1:c.97C>G, XM_047435431.1:c.226C>G, NP_036272.2:p.Leu76Val, NP_001257817.1:p.Leu76Val, NP_001257882.1:p.Leu76Val, XP_047291388.1:p.Leu33Val, XP_047291387.1:p.Leu76Val

Select item 14700773157.

rs1470077315 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 17:81717062 (GRCh38)
17:79684092 (GRCh37)
Canonical SPDI:: NC_000017.11:81717061:C:A,NC_000017.11:81717061:C:T
Gene:: SLC25A10 (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)
HGVS:: NC_000017.11:g.81717062C>A, NC_000017.11:g.81717062C>T, NC_000017.10:g.79684092C>A, NC_000017.10:g.79684092C>T, NM_012140.5:c.524C>A, NM_012140.5:c.524C>T, NM_012140.4:c.524C>A, NM_012140.4:c.524C>T, NM_001270888.2:c.524C>A, NM_001270888.2:c.524C>T, NM_001270888.1:c.524C>A, NM_001270888.1:c.524C>T, NM_001270953.2:c.524C>A, NM_001270953.2:c.524C>T, NM_001270953.1:c.524C>A, NM_001270953.1:c.524C>T, XM_047435432.1:c.395C>A, XM_047435432.1:c.395C>T, XM_047435431.1:c.524C>A, XM_047435431.1:c.524C>T, NP_036272.2:p.Thr175Asn, NP_036272.2:p.Thr175Ile, NP_001257817.1:p.Thr175Asn, NP_001257817.1:p.Thr175Ile, NP_001257882.1:p.Thr175Asn, NP_001257882.1:p.Thr175Ile, XP_047291388.1:p.Thr132Asn, XP_047291388.1:p.Thr132Ile, XP_047291387.1:p.Thr175Asn, XP_047291387.1:p.Thr175Ile

Select item 14670824088.

rs1467082408 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:81712498 (GRCh38)
17:79679528 (GRCh37)
Canonical SPDI:: NC_000017.11:81712497:G:A
Gene:: SLC25A10 (Varview)
Functional Consequence:: synonymous_variant,genic_upstream_transcript_variant,upstream_transcript_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.81712498G>A, NC_000017.10:g.79679528G>A, NM_012140.5:c.72G>A, NM_012140.4:c.72G>A, NM_001270888.2:c.72G>A, NM_001270888.1:c.72G>A, NM_001270953.2:c.72G>A, NM_001270953.1:c.72G>A, XM_047435431.1:c.72G>A

Select item 14631989899.

rs1463198989 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:81717473 (GRCh38)
17:79684503 (GRCh37)
Canonical SPDI:: NC_000017.11:81717472:T:C
Gene:: SLC25A10 (Varview)
Functional Consequence:: synonymous_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.81717473T>C, NC_000017.10:g.79684503T>C, NM_012140.5:c.609T>C, NM_012140.4:c.609T>C, NM_001270888.2:c.609T>C, NM_001270888.1:c.609T>C, XM_047435432.1:c.480T>C, XM_047435431.1:c.609T>C

Select item 145700479010.

rs1457004790 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 17:81715552 (GRCh38)
17:79682582 (GRCh37)
Canonical SPDI:: NC_000017.11:81715551:T:G
Gene:: SLC25A10 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000017.11:g.81715552T>G, NC_000017.10:g.79682582T>G, NM_012140.5:c.288T>G, NM_012140.4:c.288T>G, NM_001270888.2:c.288T>G, NM_001270888.1:c.288T>G, NM_001270953.2:c.288T>G, NM_001270953.1:c.288T>G, XM_047435432.1:c.159T>G, XM_047435431.1:c.288T>G

Select item 145564036711.

rs1455640367 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:81717435 (GRCh38)
17:79684465 (GRCh37)
Canonical SPDI:: NC_000017.11:81717434:A:G
Gene:: SLC25A10 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000016/4 (GnomAD_exomes)
G=0.000023/6 (TOPMED)
HGVS:: NC_000017.11:g.81717435A>G, NC_000017.10:g.79684465A>G, NM_012140.5:c.571A>G, NM_012140.4:c.571A>G, NM_001270888.2:c.571A>G, NM_001270888.1:c.571A>G, XM_047435432.1:c.442A>G, XM_047435431.1:c.571A>G, NP_036272.2:p.Ser191Gly, NP_001257817.1:p.Ser191Gly, XP_047291388.1:p.Ser148Gly, XP_047291387.1:p.Ser191Gly

Select item 145381602312.

rs1453816023 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 17:81717786 (GRCh38)
17:79684816 (GRCh37)
Canonical SPDI:: NC_000017.11:81717785:T:G
Gene:: SLC25A10 (Varview)
Functional Consequence:: synonymous_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.81717786T>G, NC_000017.10:g.79684816T>G, NM_012140.5:c.630T>G, NM_012140.4:c.630T>G, NM_001270888.2:c.657T>G, NM_001270888.1:c.657T>G, NM_001270953.2:c.547T>G, NM_001270953.1:c.547T>G, XM_047435432.1:c.501T>G, XM_047435431.1:c.630T>G, NP_001257882.1:p.Trp183Gly

Select item 145058961813.

rs1450589618 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:81715070 (GRCh38)
17:79682100 (GRCh37)
Canonical SPDI:: NC_000017.11:81715069:C:T
Gene:: SLC25A10 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000026/7 (TOPMED)
T=0.000036/5 (GnomAD)
HGVS:: NC_000017.11:g.81715070C>T, NC_000017.10:g.79682100C>T, NM_012140.5:c.211C>T, NM_012140.4:c.211C>T, NM_001270888.2:c.211C>T, NM_001270888.1:c.211C>T, NM_001270953.2:c.211C>T, NM_001270953.1:c.211C>T, XM_047435432.1:c.82C>T, XM_047435431.1:c.211C>T, NP_036272.2:p.Gln71Ter, NP_001257817.1:p.Gln71Ter, NP_001257882.1:p.Gln71Ter, XP_047291388.1:p.Gln28Ter, XP_047291387.1:p.Gln71Ter

Select item 144887494514.

rs1448874945 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 17:81715580 (GRCh38)
17:79682610 (GRCh37)
Canonical SPDI:: NC_000017.11:81715579:G:C,NC_000017.11:81715579:G:T
Gene:: SLC25A10 (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)
HGVS:: NC_000017.11:g.81715580G>C, NC_000017.11:g.81715580G>T, NC_000017.10:g.79682610G>C, NC_000017.10:g.79682610G>T, NM_012140.5:c.316G>C, NM_012140.5:c.316G>T, NM_012140.4:c.316G>C, NM_012140.4:c.316G>T, NM_001270888.2:c.316G>C, NM_001270888.2:c.316G>T, NM_001270888.1:c.316G>C, NM_001270888.1:c.316G>T, NM_001270953.2:c.316G>C, NM_001270953.2:c.316G>T, NM_001270953.1:c.316G>C, NM_001270953.1:c.316G>T, XM_047435432.1:c.187G>C, XM_047435432.1:c.187G>T, XM_047435431.1:c.316G>C, XM_047435431.1:c.316G>T, NP_036272.2:p.Gly106Arg, NP_036272.2:p.Gly106Cys, NP_001257817.1:p.Gly106Arg, NP_001257817.1:p.Gly106Cys, NP_001257882.1:p.Gly106Arg, NP_001257882.1:p.Gly106Cys, XP_047291388.1:p.Gly63Arg, XP_047291388.1:p.Gly63Cys, XP_047291387.1:p.Gly106Arg, XP_047291387.1:p.Gly106Cys

Select item 144319559215.

rs1443195592 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:81719851 (GRCh38)
17:79686881 (GRCh37)
Canonical SPDI:: NC_000017.11:81719850:G:T
Gene:: SLC25A10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant,stop_gained
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.81719851G>T, NC_000017.10:g.79686881G>T, NM_012140.5:c.726G>T, NM_012140.4:c.726G>T, NM_001270888.2:c.753G>T, NM_001270888.1:c.753G>T, NM_001270953.2:c.643G>T, NM_001270953.1:c.643G>T, XM_047435432.1:c.597G>T, NP_001257882.1:p.Gly215Ter

Select item 144290471316.

rs1442904713 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:81716846 (GRCh38)
17:79683876 (GRCh37)
Canonical SPDI:: NC_000017.11:81716845:G:C
Gene:: SLC25A10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000017.11:g.81716846G>C, NC_000017.10:g.79683876G>C, NM_012140.5:c.454G>C, NM_012140.4:c.454G>C, NM_001270888.2:c.454G>C, NM_001270888.1:c.454G>C, NM_001270953.2:c.454G>C, NM_001270953.1:c.454G>C, XM_047435432.1:c.325G>C, XM_047435431.1:c.454G>C, NP_036272.2:p.Ala152Pro, NP_001257817.1:p.Ala152Pro, NP_001257882.1:p.Ala152Pro, XP_047291388.1:p.Ala109Pro, XP_047291387.1:p.Ala152Pro

Select item 143724354317.

rs1437243543 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:81712491 (GRCh38)
17:79679521 (GRCh37)
Canonical SPDI:: NC_000017.11:81712490:G:A
Gene:: SLC25A10 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,coding_sequence_variant,missense_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000017.11:g.81712491G>A, NC_000017.10:g.79679521G>A, NM_012140.5:c.65G>A, NM_012140.4:c.65G>A, NM_001270888.2:c.65G>A, NM_001270888.1:c.65G>A, NM_001270953.2:c.65G>A, NM_001270953.1:c.65G>A, XM_047435431.1:c.65G>A, NP_036272.2:p.Cys22Tyr, NP_001257817.1:p.Cys22Tyr, NP_001257882.1:p.Cys22Tyr, XP_047291387.1:p.Cys22Tyr

Select item 142853092618.

rs1428530926 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:81719993 (GRCh38)
17:79687023 (GRCh37)
Canonical SPDI:: NC_000017.11:81719992:C:T
Gene:: SLC25A10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.81719993C>T, NC_000017.10:g.79687023C>T, NM_012140.5:c.780C>T, NM_012140.4:c.780C>T, NM_001270888.2:c.807C>T, NM_001270888.1:c.807C>T, NM_001270953.2:c.697C>T, NM_001270953.1:c.697C>T, XM_047435432.1:c.651C>T, NP_001257882.1:p.His233Tyr

Select item 142250426019.

rs1422504260 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:81712486 (GRCh38)
17:79679516 (GRCh37)
Canonical SPDI:: NC_000017.11:81712485:C:T
Gene:: SLC25A10 (Varview)
Functional Consequence:: synonymous_variant,genic_upstream_transcript_variant,upstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.00003/8 (TOPMED)
HGVS:: NC_000017.11:g.81712486C>T, NC_000017.10:g.79679516C>T, NM_012140.5:c.60C>T, NM_012140.4:c.60C>T, NM_001270888.2:c.60C>T, NM_001270888.1:c.60C>T, NM_001270953.2:c.60C>T, NM_001270953.1:c.60C>T, XM_047435431.1:c.60C>T

Select item 142146630420.

rs1421466304 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:81719847 (GRCh38)
17:79686877 (GRCh37)
Canonical SPDI:: NC_000017.11:81719846:C:T
Gene:: SLC25A10 (Varview)
Functional Consequence:: synonymous_variant,genic_downstream_transcript_variant,missense_variant,coding_sequence_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_000017.11:g.81719847C>T, NC_000017.10:g.79686877C>T, NM_012140.5:c.722C>T, NM_012140.4:c.722C>T, NM_001270888.2:c.749C>T, NM_001270888.1:c.749C>T, NM_001270953.2:c.639C>T, NM_001270953.1:c.639C>T, XM_047435432.1:c.593C>T, NP_036272.2:p.Ala241Val, NP_001257817.1:p.Ala250Val, XP_047291388.1:p.Ala198Val

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