SNP Links for Protein (Select 224548983) - SNP

Links from Protein

Items: 1 to 20 of 181

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Select item 14848033941.

rs1484803394 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 13:108270074 (GRCh38)
13:108922422 (GRCh37)
Canonical SPDI:: NC_000013.11:108270073:G:C
Gene:: TNFSF13B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000013.11:g.108270074G>C, NC_000013.10:g.108922422G>C, NG_029524.1:g.5446G>C, NM_006573.5:c.179G>C, NM_006573.4:c.179G>C, NM_001145645.2:c.179G>C, XM_047430055.1:c.179G>C, NP_006564.1:p.Cys60Ser, NP_001139117.1:p.Cys60Ser, XP_047286011.1:p.Cys60Ser

Select item 14820304132.

rs1482030413 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 13:108269925 (GRCh38)
13:108922273 (GRCh37)
Canonical SPDI:: NC_000013.11:108269924:A:T
Gene:: TNFSF13B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.108269925A>T, NC_000013.10:g.108922273A>T, NG_029524.1:g.5297A>T, NM_006573.5:c.30A>T, NM_006573.4:c.30A>T, NM_001145645.2:c.30A>T, XM_047430055.1:c.30A>T

Select item 14762831173.

rs1476283117 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 13:108270133 (GRCh38)
13:108922481 (GRCh37)
Canonical SPDI:: NC_000013.11:108270132:C:A,NC_000013.11:108270132:C:T
Gene:: TNFSF13B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.108270133C>A, NC_000013.11:g.108270133C>T, NC_000013.10:g.108922481C>A, NC_000013.10:g.108922481C>T, NG_029524.1:g.5505C>A, NG_029524.1:g.5505C>T, NM_006573.5:c.238C>A, NM_006573.5:c.238C>T, NM_006573.4:c.238C>A, NM_006573.4:c.238C>T, NM_001145645.2:c.238C>A, NM_001145645.2:c.238C>T, XM_047430055.1:c.238C>A, XM_047430055.1:c.238C>T, NP_006564.1:p.Arg80Trp, NP_001139117.1:p.Arg80Trp, XP_047286011.1:p.Arg80Trp

Select item 14751811854.

rs1475181185 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:108270033 (GRCh38)
13:108922381 (GRCh37)
Canonical SPDI:: NC_000013.11:108270032:G:A
Gene:: TNFSF13B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.108270033G>A, NC_000013.10:g.108922381G>A, NG_029524.1:g.5405G>A, NM_006573.5:c.138G>A, NM_006573.4:c.138G>A, NM_001145645.2:c.138G>A, XM_047430055.1:c.138G>A

Select item 14652669245.

rs1465266924 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:108270396 (GRCh38)
13:108922744 (GRCh37)
Canonical SPDI:: NC_000013.11:108270395:G:A
Gene:: TNFSF13B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.108270396G>A, NC_000013.10:g.108922744G>A, NG_029524.1:g.5768G>A, NM_006573.5:c.396G>A, NM_006573.4:c.396G>A, NM_001145645.2:c.396G>A, XM_047430055.1:c.396G>A

Select item 14647523126.

rs1464752312 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:108270391 (GRCh38)
13:108922739 (GRCh37)
Canonical SPDI:: NC_000013.11:108270390:A:G
Gene:: TNFSF13B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.108270391A>G, NC_000013.10:g.108922739A>G, NG_029524.1:g.5763A>G, NM_006573.5:c.391A>G, NM_006573.4:c.391A>G, NM_001145645.2:c.391A>G, XM_047430055.1:c.391A>G, NP_006564.1:p.Asn131Asp, NP_001139117.1:p.Asn131Asp, XP_047286011.1:p.Asn131Asp

Select item 14572960727.

rs1457296072 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:108303604 (GRCh38)
13:108955952 (GRCh37)
Canonical SPDI:: NC_000013.11:108303603:G:A
Gene:: TNFSF13B (Varview)
Functional Consequence:: missense_variant,downstream_transcript_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.108303604G>A, NC_000013.10:g.108955952G>A, NG_029524.1:g.38976G>A, NM_006573.5:c.745G>A, NM_006573.4:c.745G>A, NM_001145645.2:c.688G>A, NP_006564.1:p.Gly249Ser, NP_001139117.1:p.Gly230Ser

Select item 14389952868.

rs1438995286 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:108303467 (GRCh38)
13:108955815 (GRCh37)
Canonical SPDI:: NC_000013.11:108303466:A:G
Gene:: TNFSF13B (Varview)
Functional Consequence:: downstream_transcript_variant,genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.108303467A>G, NC_000013.10:g.108955815A>G, NG_029524.1:g.38839A>G, NM_006573.5:c.608A>G, NM_006573.4:c.608A>G, NM_001145645.2:c.551A>G, NP_006564.1:p.Asp203Gly, NP_001139117.1:p.Asp184Gly

Select item 14351394149.

rs1435139414 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 13:108269989 (GRCh38)
13:108922337 (GRCh37)
Canonical SPDI:: NC_000013.11:108269988:C:G,NC_000013.11:108269988:C:T
Gene:: TNFSF13B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000013.11:g.108269989C>G, NC_000013.11:g.108269989C>T, NC_000013.10:g.108922337C>G, NC_000013.10:g.108922337C>T, NG_029524.1:g.5361C>G, NG_029524.1:g.5361C>T, NM_006573.5:c.94C>G, NM_006573.5:c.94C>T, NM_006573.4:c.94C>G, NM_006573.4:c.94C>T, NM_001145645.2:c.94C>G, NM_001145645.2:c.94C>T, XM_047430055.1:c.94C>G, XM_047430055.1:c.94C>T, NP_006564.1:p.Pro32Ala, NP_006564.1:p.Pro32Ser, NP_001139117.1:p.Pro32Ala, NP_001139117.1:p.Pro32Ser, XP_047286011.1:p.Pro32Ala, XP_047286011.1:p.Pro32Ser

Select item 143333264010.

rs1433332640 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:108270163 (GRCh38)
13:108922511 (GRCh37)
Canonical SPDI:: NC_000013.11:108270162:A:G
Gene:: TNFSF13B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.108270163A>G, NC_000013.10:g.108922511A>G, NG_029524.1:g.5535A>G, NM_006573.5:c.268A>G, NM_006573.4:c.268A>G, NM_001145645.2:c.268A>G, XM_047430055.1:c.268A>G, NP_006564.1:p.Lys90Glu, NP_001139117.1:p.Lys90Glu, XP_047286011.1:p.Lys90Glu

Select item 143310625111.

rs1433106251 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 13:108303568 (GRCh38)
13:108955916 (GRCh37)
Canonical SPDI:: NC_000013.11:108303567:C:A
Gene:: TNFSF13B (Varview)
Functional Consequence:: downstream_transcript_variant,genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000013.11:g.108303568C>A, NC_000013.10:g.108955916C>A, NG_029524.1:g.38940C>A, NM_006573.5:c.709C>A, NM_006573.4:c.709C>A, NM_001145645.2:c.652C>A, NP_006564.1:p.Pro237Thr, NP_001139117.1:p.Pro218Thr

Select item 142049360512.

rs1420493605 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 13:108270147 (GRCh38)
13:108922495 (GRCh37)
Canonical SPDI:: NC_000013.11:108270146:G:C
Gene:: TNFSF13B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.108270147G>C, NC_000013.10:g.108922495G>C, NG_029524.1:g.5519G>C, NM_006573.5:c.252G>C, NM_006573.4:c.252G>C, NM_001145645.2:c.252G>C, XM_047430055.1:c.252G>C, NP_006564.1:p.Gln84His, NP_001139117.1:p.Gln84His, XP_047286011.1:p.Gln84His

Select item 142047953313.

rs1420479533 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 13:108270014 (GRCh38)
13:108922362 (GRCh37)
Canonical SPDI:: NC_000013.11:108270013:G:T
Gene:: TNFSF13B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000013.11:g.108270014G>T, NC_000013.10:g.108922362G>T, NG_029524.1:g.5386G>T, NM_006573.5:c.119G>T, NM_006573.4:c.119G>T, NM_001145645.2:c.119G>T, XM_047430055.1:c.119G>T, NP_006564.1:p.Arg40Leu, NP_001139117.1:p.Arg40Leu, XP_047286011.1:p.Arg40Leu

Select item 142023295314.

rs1420232953 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:108270202 (GRCh38)
13:108922550 (GRCh37)
Canonical SPDI:: NC_000013.11:108270201:G:A
Gene:: TNFSF13B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.108270202G>A, NC_000013.10:g.108922550G>A, NG_029524.1:g.5574G>A, NM_006573.5:c.307G>A, NM_006573.4:c.307G>A, NM_001145645.2:c.307G>A, XM_047430055.1:c.307G>A, NP_006564.1:p.Glu103Lys, NP_001139117.1:p.Glu103Lys, XP_047286011.1:p.Glu103Lys

Select item 141668475815.

rs1416684758 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:108270351 (GRCh38)
13:108922699 (GRCh37)
Canonical SPDI:: NC_000013.11:108270350:A:G
Gene:: TNFSF13B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.108270351A>G, NC_000013.10:g.108922699A>G, NG_029524.1:g.5723A>G, NM_006573.5:c.351A>G, NM_006573.4:c.351A>G, NM_001145645.2:c.351A>G, XM_047430055.1:c.351A>G

Select item 141642975216.

rs1416429752 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:108303485 (GRCh38)
13:108955833 (GRCh37)
Canonical SPDI:: NC_000013.11:108303484:G:A
Gene:: TNFSF13B (Varview)
Functional Consequence:: genic_downstream_transcript_variant,missense_variant,downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.108303485G>A, NC_000013.10:g.108955833G>A, NG_029524.1:g.38857G>A, NM_006573.5:c.626G>A, NM_006573.4:c.626G>A, NM_001145645.2:c.569G>A, NP_006564.1:p.Gly209Glu, NP_001139117.1:p.Gly190Glu

Select item 141233161517.

rs1412331615 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:108270037 (GRCh38)
13:108922385 (GRCh37)
Canonical SPDI:: NC_000013.11:108270036:C:T
Gene:: TNFSF13B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.108270037C>T, NC_000013.10:g.108922385C>T, NG_029524.1:g.5409C>T, NM_006573.5:c.142C>T, NM_006573.4:c.142C>T, NM_001145645.2:c.142C>T, XM_047430055.1:c.142C>T

Select item 140645731818.

rs1406457318 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:108306854 (GRCh38)
13:108959202 (GRCh37)
Canonical SPDI:: NC_000013.11:108306853:A:G
Gene:: TNFSF13B (Varview)
Functional Consequence:: synonymous_variant,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
G=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000013.11:g.108306854A>G, NC_000013.10:g.108959202A>G, NG_029524.1:g.42226A>G, NM_006573.5:c.774A>G, NM_006573.4:c.774A>G, NM_001145645.2:c.717A>G

Select item 139780285619.

rs1397802856 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 13:108270228 (GRCh38)
13:108922576 (GRCh37)
Canonical SPDI:: NC_000013.11:108270227:A:C
Gene:: TNFSF13B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.108270228A>C, NC_000013.10:g.108922576A>C, NG_029524.1:g.5600A>C, NM_006573.5:c.333A>C, NM_006573.4:c.333A>C, NM_001145645.2:c.333A>C, XM_047430055.1:c.333A>C

Select item 138963876520.

rs1389638765 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:108303320 (GRCh38)
13:108955668 (GRCh37)
Canonical SPDI:: NC_000013.11:108303319:T:C
Gene:: TNFSF13B (Varview)
Functional Consequence:: coding_sequence_variant,3_prime_UTR_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000013.11:g.108303320T>C, NC_000013.10:g.108955668T>C, NG_029524.1:g.38692T>C, NM_006573.5:c.549T>C, NM_006573.4:c.549T>C, NM_001145645.2:c.492T>C, XM_047430055.1:c.*67T>C

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