SNP Links for Nucleotide (Select 295849295) - SNP

Links from Nucleotide

Items: 1 to 20 of 594

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Select item 14907377441.

rs1490737744 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:89384988 (GRCh38)
10:91144745 (GRCh37)
Canonical SPDI:: NC_000010.11:89384987:A:C
Gene:: IFIT1B (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.89384988A>C, NC_000010.10:g.91144745A>C, NM_001010987.2:c.*250A>C

Select item 14879508802.

rs1487950880 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:89384287 (GRCh38)
10:91144044 (GRCh37)
Canonical SPDI:: NC_000010.11:89384286:C:T
Gene:: IFIT1B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.89384287C>T, NC_000010.10:g.91144044C>T, NM_001010987.2:c.974C>T, NP_001010987.1:p.Ala325Val

Select item 14878090603.

rs1487809060 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:89383410 (GRCh38)
10:91143167 (GRCh37)
Canonical SPDI:: NC_000010.11:89383409:C:G
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000010.11:g.89383410C>G, NC_000010.10:g.91143167C>G, NM_001010987.2:c.97C>G, NP_001010987.1:p.Pro33Ala

Select item 14868314354.

rs1486831435 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:89383451 (GRCh38)
10:91143208 (GRCh37)
Canonical SPDI:: NC_000010.11:89383450:G:A
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.89383451G>A, NC_000010.10:g.91143208G>A, NM_001010987.2:c.138G>A

Select item 14840514765.

rs1484051476 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 10:89384688 (GRCh38)
10:91144445 (GRCh37)
Canonical SPDI:: NC_000010.11:89384687:T:G
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.89384688T>G, NC_000010.10:g.91144445T>G, NM_001010987.2:c.1375T>G, NP_001010987.1:p.Cys459Gly

Select item 14837229986.

rs1483722998 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:89383327 (GRCh38)
10:91143084 (GRCh37)
Canonical SPDI:: NC_000010.11:89383326:C:A
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000010.11:g.89383327C>A, NC_000010.10:g.91143084C>A, NM_001010987.2:c.14C>A, NP_001010987.1:p.Ser5Tyr

Select item 14836548497.

rs1483654849 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 10:89385036 (GRCh38)
10:91144793 (GRCh37)
Canonical SPDI:: NC_000010.11:89385035:A:T
Gene:: IFIT1B (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.89385036A>T, NC_000010.10:g.91144793A>T, NM_001010987.2:c.*298A>T

Select item 14835506128.

rs1483550612 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 10:89384860 (GRCh38)
10:91144617 (GRCh37)
Canonical SPDI:: NC_000010.11:89384859:G:A,NC_000010.11:89384859:G:T
Gene:: IFIT1B (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000010.11:g.89384860G>A, NC_000010.11:g.89384860G>T, NC_000010.10:g.91144617G>A, NC_000010.10:g.91144617G>T, NM_001010987.2:c.*122G>A, NM_001010987.2:c.*122G>T

Select item 14826963579.

rs1482696357 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:89384761 (GRCh38)
10:91144518 (GRCh37)
Canonical SPDI:: NC_000010.11:89384760:T:C
Gene:: IFIT1B (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency
MAF:: C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.89384761T>C, NC_000010.10:g.91144518T>C, NM_001010987.2:c.*23T>C

Select item 148172396910.

rs1481723969 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:89383977 (GRCh38)
10:91143734 (GRCh37)
Canonical SPDI:: NC_000010.11:89383976:C:A
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.89383977C>A, NC_000010.10:g.91143734C>A, NM_001010987.2:c.664C>A, NP_001010987.1:p.Leu222Ile

Select item 148155725711.

rs1481557257 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:89384393 (GRCh38)
10:91144150 (GRCh37)
Canonical SPDI:: NC_000010.11:89384392:G:A
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.89384393G>A, NC_000010.10:g.91144150G>A, NM_001010987.2:c.1080G>A

Select item 148060341412.

rs1480603414 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:89384736 (GRCh38)
10:91144493 (GRCh37)
Canonical SPDI:: NC_000010.11:89384735:T:C
Gene:: IFIT1B (Varview)
Functional Consequence:: terminator_codon_variant,stop_lost
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.89384736T>C, NC_000010.10:g.91144493T>C, NM_001010987.2:c.1423T>C, NP_001010987.1:p.Ter475Gln

Select item 147645366913.

rs1476453669 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 10:89384379 (GRCh38)
10:91144136 (GRCh37)
Canonical SPDI:: NC_000010.11:89384378:C:A,NC_000010.11:89384378:C:G
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
A=0.000142/2 (TOMMO)
HGVS:: NC_000010.11:g.89384379C>A, NC_000010.11:g.89384379C>G, NC_000010.10:g.91144136C>A, NC_000010.10:g.91144136C>G, NM_001010987.2:c.1066C>A, NM_001010987.2:c.1066C>G, NP_001010987.1:p.His356Asn, NP_001010987.1:p.His356Asp

Select item 147525209914.

rs1475252099 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:89383801 (GRCh38)
10:91143558 (GRCh37)
Canonical SPDI:: NC_000010.11:89383800:G:A,NC_000010.11:89383800:G:C
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000028/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.89383801G>A, NC_000010.11:g.89383801G>C, NC_000010.10:g.91143558G>A, NC_000010.10:g.91143558G>C, NM_001010987.2:c.488G>A, NM_001010987.2:c.488G>C, NP_001010987.1:p.Cys163Tyr, NP_001010987.1:p.Cys163Ser

Select item 147321929915.

rs1473219299 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:89384975 (GRCh38)
10:91144732 (GRCh37)
Canonical SPDI:: NC_000010.11:89384974:G:A
Gene:: IFIT1B (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.89384975G>A, NC_000010.10:g.91144732G>A, NM_001010987.2:c.*237G>A

Select item 147224474016.

rs1472244740 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:89384276 (GRCh38)
10:91144033 (GRCh37)
Canonical SPDI:: NC_000010.11:89384275:G:A
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.89384276G>A, NC_000010.10:g.91144033G>A, NM_001010987.2:c.963G>A

Select item 147190973717.

rs1471909737 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 10:89384291 (GRCh38)
10:91144048 (GRCh37)
Canonical SPDI:: NC_000010.11:89384290:A:T
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000010.11:g.89384291A>T, NC_000010.10:g.91144048A>T, NM_001010987.2:c.978A>T

Select item 146884601018.

rs1468846010 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:89383526 (GRCh38)
10:91143283 (GRCh37)
Canonical SPDI:: NC_000010.11:89383525:C:G
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.89383526C>G, NC_000010.10:g.91143283C>G, NM_001010987.2:c.213C>G

Select item 146814277819.

rs1468142778 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:89384593 (GRCh38)
10:91144350 (GRCh37)
Canonical SPDI:: NC_000010.11:89384592:A:G
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000010.11:g.89384593A>G, NC_000010.10:g.91144350A>G, NM_001010987.2:c.1280A>G, NP_001010987.1:p.Lys427Arg

Select item 146738794820.

rs1467387948 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:89383934 (GRCh38)
10:91143691 (GRCh37)
Canonical SPDI:: NC_000010.11:89383933:A:G
Gene:: IFIT1B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.89383934A>G, NC_000010.10:g.91143691A>G, NM_001010987.2:c.621A>G

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