SNP Links for Protein (Select 1034575971) - SNP

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:5667911 (GRCh38)
11:5689141 (GRCh37)
Canonical SPDI:: NC_000011.10:5667910:A:G
Gene:: TRIM5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000019/5 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.5667911A>G, NC_000011.9:g.5689141A>G, NG_029122.1:g.22199T>C, XM_017018460.3:c.933T>C, XM_017018460.2:c.933T>C, XM_017018460.1:c.933T>C

Select item 146851813011.

rs1468518130 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:5679785 (GRCh38)
11:5701015 (GRCh37)
Canonical SPDI:: NC_000011.10:5679784:T:C
Gene:: TRIM5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.5679785T>C, NC_000011.9:g.5701015T>C, NG_029122.1:g.10325A>G, NM_033092.4:c.393A>G, NM_033092.3:c.393A>G, NM_033092.2:c.393A>G, NM_033093.4:c.393A>G, NM_033093.3:c.393A>G, NM_033093.2:c.393A>G, NM_033034.3:c.393A>G, NM_033034.2:c.393A>G, NM_001410958.1:c.393A>G, XM_006718358.4:c.393A>G, XM_006718358.3:c.393A>G, XM_006718358.2:c.393A>G, XM_006718358.1:c.393A>G, XM_005253183.4:c.393A>G, XM_005253183.3:c.393A>G, XM_005253183.2:c.393A>G, XM_005253183.1:c.393A>G, XM_005253184.4:c.393A>G, XM_005253184.3:c.393A>G, XM_005253184.2:c.393A>G, XM_005253184.1:c.393A>G, XM_011520426.4:c.393A>G, XM_011520426.3:c.393A>G, XM_011520426.2:c.393A>G, XM_011520426.1:c.393A>G, XR_001748014.3:n.661A>G, XR_001748014.2:n.671A>G, XR_001748014.1:n.682A>G, XM_017018463.3:c.393A>G, XM_017018461.3:c.393A>G, XM_017018461.2:c.393A>G, XM_017018461.1:c.393A>G, XM_017018460.3:c.393A>G, XM_017018460.2:c.393A>G, XM_017018460.1:c.393A>G, XR_007062519.1:n.661A>G, XR_007062518.1:n.513A>G, XR_007062522.1:n.513A>G, XM_047427784.1:c.393A>G, XM_047427783.1:c.393A>G, XR_007062517.1:n.661A>G, XR_007062520.1:n.661A>G, XR_007062521.1:n.513A>G

Select item 146684691212.

rs1466846912 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:5678205 (GRCh38)
11:5699435 (GRCh37)
Canonical SPDI:: NC_000011.10:5678204:T:A
Gene:: TRIM5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000007/1 (GnomAD)
A=0.00002/5 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5678205T>A, NC_000011.9:g.5699435T>A, NG_029122.1:g.11905A>T, NM_033092.4:c.743A>T, NM_033092.3:c.743A>T, NM_033092.2:c.743A>T, NM_033093.4:c.743A>T, NM_033093.3:c.743A>T, NM_033093.2:c.743A>T, NM_033034.3:c.743A>T, NM_033034.2:c.743A>T, NM_001410958.1:c.743A>T, XM_006718358.4:c.743A>T, XM_006718358.3:c.743A>T, XM_006718358.2:c.743A>T, XM_006718358.1:c.743A>T, XM_005253183.4:c.743A>T, XM_005253183.3:c.743A>T, XM_005253183.2:c.743A>T, XM_005253183.1:c.743A>T, XM_005253184.4:c.743A>T, XM_005253184.3:c.743A>T, XM_005253184.2:c.743A>T, XM_005253184.1:c.743A>T, XM_011520426.4:c.743A>T, XM_011520426.3:c.743A>T, XM_011520426.2:c.743A>T, XM_011520426.1:c.743A>T, XR_001748014.3:n.1011A>T, XR_001748014.2:n.1021A>T, XR_001748014.1:n.1032A>T, XM_017018463.3:c.743A>T, XM_017018461.3:c.743A>T, XM_017018461.2:c.743A>T, XM_017018461.1:c.743A>T, XM_017018460.3:c.743A>T, XM_017018460.2:c.743A>T, XM_017018460.1:c.743A>T, XR_007062519.1:n.1011A>T, XR_007062518.1:n.863A>T, XR_007062522.1:n.863A>T, XM_047427784.1:c.743A>T, XM_047427783.1:c.743A>T, XR_007062517.1:n.1011A>T, XR_007062520.1:n.1011A>T, XR_007062521.1:n.863A>T, NP_149083.2:p.Gln248Leu, NP_149084.2:p.Gln248Leu, NP_149023.2:p.Gln248Leu, XP_006718421.1:p.Gln248Leu, XP_005253240.1:p.Gln248Leu, XP_005253241.1:p.Gln248Leu, XP_011518728.1:p.Gln248Leu, XP_016873952.1:p.Gln248Leu, XP_016873950.1:p.Gln248Leu, XP_016873949.1:p.Gln248Leu, XP_047283740.1:p.Gln248Leu, XP_047283739.1:p.Gln248Leu

Select item 146312783313.

rs1463127833 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:5667908 (GRCh38)
11:5689138 (GRCh37)
Canonical SPDI:: NC_000011.10:5667907:G:C
Gene:: TRIM5 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.5667908G>C, NC_000011.9:g.5689138G>C, NG_029122.1:g.22202C>G, XM_017018460.3:c.936C>G, XM_017018460.2:c.936C>G, XM_017018460.1:c.936C>G, XP_016873949.1:p.Phe312Leu

Select item 146249651214.

rs1462496512 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:5680097 (GRCh38)
11:5701327 (GRCh37)
Canonical SPDI:: NC_000011.10:5680096:G:C
Gene:: TRIM5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000028/1 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.5680097G>C, NC_000011.9:g.5701327G>C, NG_029122.1:g.10013C>G, NM_033092.4:c.81C>G, NM_033092.3:c.81C>G, NM_033092.2:c.81C>G, NM_033093.4:c.81C>G, NM_033093.3:c.81C>G, NM_033093.2:c.81C>G, NM_033034.3:c.81C>G, NM_033034.2:c.81C>G, NM_001410958.1:c.81C>G, XM_006718358.4:c.81C>G, XM_006718358.3:c.81C>G, XM_006718358.2:c.81C>G, XM_006718358.1:c.81C>G, XM_005253183.4:c.81C>G, XM_005253183.3:c.81C>G, XM_005253183.2:c.81C>G, XM_005253183.1:c.81C>G, XM_005253184.4:c.81C>G, XM_005253184.3:c.81C>G, XM_005253184.2:c.81C>G, XM_005253184.1:c.81C>G, XM_011520426.4:c.81C>G, XM_011520426.3:c.81C>G, XM_011520426.2:c.81C>G, XM_011520426.1:c.81C>G, XR_001748014.3:n.349C>G, XR_001748014.2:n.359C>G, XR_001748014.1:n.370C>G, XM_017018463.3:c.81C>G, XM_017018461.3:c.81C>G, XM_017018461.2:c.81C>G, XM_017018461.1:c.81C>G, XM_017018460.3:c.81C>G, XM_017018460.2:c.81C>G, XM_017018460.1:c.81C>G, XR_007062519.1:n.349C>G, XR_007062518.1:n.201C>G, XR_007062522.1:n.201C>G, XM_047427784.1:c.81C>G, XM_047427783.1:c.81C>G, XR_007062517.1:n.349C>G, XR_007062520.1:n.349C>G, XR_007062521.1:n.201C>G, NP_149083.2:p.Ser27Arg, NP_149084.2:p.Ser27Arg, NP_149023.2:p.Ser27Arg, XP_006718421.1:p.Ser27Arg, XP_005253240.1:p.Ser27Arg, XP_005253241.1:p.Ser27Arg, XP_011518728.1:p.Ser27Arg, XP_016873952.1:p.Ser27Arg, XP_016873950.1:p.Ser27Arg, XP_016873949.1:p.Ser27Arg, XP_047283740.1:p.Ser27Arg, XP_047283739.1:p.Ser27Arg

Select item 145793909415.

rs1457939094 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:5679881 (GRCh38)
11:5701111 (GRCh37)
Canonical SPDI:: NC_000011.10:5679880:T:C
Gene:: TRIM5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5679881T>C, NC_000011.9:g.5701111T>C, NG_029122.1:g.10229A>G, NM_033092.4:c.297A>G, NM_033092.3:c.297A>G, NM_033092.2:c.297A>G, NM_033093.4:c.297A>G, NM_033093.3:c.297A>G, NM_033093.2:c.297A>G, NM_033034.3:c.297A>G, NM_033034.2:c.297A>G, NM_001410958.1:c.297A>G, XM_006718358.4:c.297A>G, XM_006718358.3:c.297A>G, XM_006718358.2:c.297A>G, XM_006718358.1:c.297A>G, XM_005253183.4:c.297A>G, XM_005253183.3:c.297A>G, XM_005253183.2:c.297A>G, XM_005253183.1:c.297A>G, XM_005253184.4:c.297A>G, XM_005253184.3:c.297A>G, XM_005253184.2:c.297A>G, XM_005253184.1:c.297A>G, XM_011520426.4:c.297A>G, XM_011520426.3:c.297A>G, XM_011520426.2:c.297A>G, XM_011520426.1:c.297A>G, XR_001748014.3:n.565A>G, XR_001748014.2:n.575A>G, XR_001748014.1:n.586A>G, XM_017018463.3:c.297A>G, XM_017018461.3:c.297A>G, XM_017018461.2:c.297A>G, XM_017018461.1:c.297A>G, XM_017018460.3:c.297A>G, XM_017018460.2:c.297A>G, XM_017018460.1:c.297A>G, XR_007062519.1:n.565A>G, XR_007062518.1:n.417A>G, XR_007062522.1:n.417A>G, XM_047427784.1:c.297A>G, XM_047427783.1:c.297A>G, XR_007062517.1:n.565A>G, XR_007062520.1:n.565A>G, XR_007062521.1:n.417A>G

Select item 144843004116.

rs1448430041 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:5680067 (GRCh38)
11:5701297 (GRCh37)
Canonical SPDI:: NC_000011.10:5680066:T:A,NC_000011.10:5680066:T:C
Gene:: TRIM5 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.5680067T>A, NC_000011.10:g.5680067T>C, NC_000011.9:g.5701297T>A, NC_000011.9:g.5701297T>C, NG_029122.1:g.10043A>T, NG_029122.1:g.10043A>G, NM_033092.4:c.111A>T, NM_033092.4:c.111A>G, NM_033092.3:c.111A>T, NM_033092.3:c.111A>G, NM_033092.2:c.111A>T, NM_033092.2:c.111A>G, NM_033093.4:c.111A>T, NM_033093.4:c.111A>G, NM_033093.3:c.111A>T, NM_033093.3:c.111A>G, NM_033093.2:c.111A>T, NM_033093.2:c.111A>G, NM_033034.3:c.111A>T, NM_033034.3:c.111A>G, NM_033034.2:c.111A>T, NM_033034.2:c.111A>G, NM_001410958.1:c.111A>T, NM_001410958.1:c.111A>G, XM_006718358.4:c.111A>T, XM_006718358.4:c.111A>G, XM_006718358.3:c.111A>T, XM_006718358.3:c.111A>G, XM_006718358.2:c.111A>T, XM_006718358.2:c.111A>G, XM_006718358.1:c.111A>T, XM_006718358.1:c.111A>G, XM_005253183.4:c.111A>T, XM_005253183.4:c.111A>G, XM_005253183.3:c.111A>T, XM_005253183.3:c.111A>G, XM_005253183.2:c.111A>T, XM_005253183.2:c.111A>G, XM_005253183.1:c.111A>T, XM_005253183.1:c.111A>G, XM_005253184.4:c.111A>T, XM_005253184.4:c.111A>G, XM_005253184.3:c.111A>T, XM_005253184.3:c.111A>G, XM_005253184.2:c.111A>T, XM_005253184.2:c.111A>G, XM_005253184.1:c.111A>T, XM_005253184.1:c.111A>G, XM_011520426.4:c.111A>T, XM_011520426.4:c.111A>G, XM_011520426.3:c.111A>T, XM_011520426.3:c.111A>G, XM_011520426.2:c.111A>T, XM_011520426.2:c.111A>G, XM_011520426.1:c.111A>T, XM_011520426.1:c.111A>G, XR_001748014.3:n.379A>T, XR_001748014.3:n.379A>G, XR_001748014.2:n.389A>T, XR_001748014.2:n.389A>G, XR_001748014.1:n.400A>T, XR_001748014.1:n.400A>G, XM_017018463.3:c.111A>T, XM_017018463.3:c.111A>G, XM_017018461.3:c.111A>T, XM_017018461.3:c.111A>G, XM_017018461.2:c.111A>T, XM_017018461.2:c.111A>G, XM_017018461.1:c.111A>T, XM_017018461.1:c.111A>G, XM_017018460.3:c.111A>T, XM_017018460.3:c.111A>G, XM_017018460.2:c.111A>T, XM_017018460.2:c.111A>G, XM_017018460.1:c.111A>T, XM_017018460.1:c.111A>G, XR_007062519.1:n.379A>T, XR_007062519.1:n.379A>G, XR_007062518.1:n.231A>T, XR_007062518.1:n.231A>G, XR_007062522.1:n.231A>T, XR_007062522.1:n.231A>G, XM_047427784.1:c.111A>T, XM_047427784.1:c.111A>G, XM_047427783.1:c.111A>T, XM_047427783.1:c.111A>G, XR_007062517.1:n.379A>T, XR_007062517.1:n.379A>G, XR_007062520.1:n.379A>T, XR_007062520.1:n.379A>G, XR_007062521.1:n.231A>T, XR_007062521.1:n.231A>G

Select item 144755679217.

rs1447556792 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:5668008 (GRCh38)
11:5689238 (GRCh37)
Canonical SPDI:: NC_000011.10:5668007:A:T
Gene:: TRIM5 (Varview)
Functional Consequence:: intron_variant,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_000011.10:g.5668008A>T, NC_000011.9:g.5689238A>T, NG_029122.1:g.22102T>A, XM_017018460.3:c.836T>A, XM_017018460.2:c.836T>A, XM_017018460.1:c.836T>A, XP_016873949.1:p.Ile279Lys

Select item 144730393218.

rs1447303932 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:5680173 (GRCh38)
11:5701403 (GRCh37)
Canonical SPDI:: NC_000011.10:5680172:G:A,NC_000011.10:5680172:G:T
Gene:: TRIM5 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5680173G>A, NC_000011.10:g.5680173G>T, NC_000011.9:g.5701403G>A, NC_000011.9:g.5701403G>T, NG_029122.1:g.9937C>T, NG_029122.1:g.9937C>A, NM_033092.4:c.5C>T, NM_033092.4:c.5C>A, NM_033092.3:c.5C>T, NM_033092.3:c.5C>A, NM_033092.2:c.5C>T, NM_033092.2:c.5C>A, NM_033093.4:c.5C>T, NM_033093.4:c.5C>A, NM_033093.3:c.5C>T, NM_033093.3:c.5C>A, NM_033093.2:c.5C>T, NM_033093.2:c.5C>A, NM_033034.3:c.5C>T, NM_033034.3:c.5C>A, NM_033034.2:c.5C>T, NM_033034.2:c.5C>A, NM_001410958.1:c.5C>T, NM_001410958.1:c.5C>A, XM_006718358.4:c.5C>T, XM_006718358.4:c.5C>A, XM_006718358.3:c.5C>T, XM_006718358.3:c.5C>A, XM_006718358.2:c.5C>T, XM_006718358.2:c.5C>A, XM_006718358.1:c.5C>T, XM_006718358.1:c.5C>A, XM_005253183.4:c.5C>T, XM_005253183.4:c.5C>A, XM_005253183.3:c.5C>T, XM_005253183.3:c.5C>A, XM_005253183.2:c.5C>T, XM_005253183.2:c.5C>A, XM_005253183.1:c.5C>T, XM_005253183.1:c.5C>A, XM_005253184.4:c.5C>T, XM_005253184.4:c.5C>A, XM_005253184.3:c.5C>T, XM_005253184.3:c.5C>A, XM_005253184.2:c.5C>T, XM_005253184.2:c.5C>A, XM_005253184.1:c.5C>T, XM_005253184.1:c.5C>A, XM_011520426.4:c.5C>T, XM_011520426.4:c.5C>A, XM_011520426.3:c.5C>T, XM_011520426.3:c.5C>A, XM_011520426.2:c.5C>T, XM_011520426.2:c.5C>A, XM_011520426.1:c.5C>T, XM_011520426.1:c.5C>A, XR_001748014.3:n.273C>T, XR_001748014.3:n.273C>A, XR_001748014.2:n.283C>T, XR_001748014.2:n.283C>A, XR_001748014.1:n.294C>T, XR_001748014.1:n.294C>A, XM_017018463.3:c.5C>T, XM_017018463.3:c.5C>A, XM_017018461.3:c.5C>T, XM_017018461.3:c.5C>A, XM_017018461.2:c.5C>T, XM_017018461.2:c.5C>A, XM_017018461.1:c.5C>T, XM_017018461.1:c.5C>A, XM_017018460.3:c.5C>T, XM_017018460.3:c.5C>A, XM_017018460.2:c.5C>T, XM_017018460.2:c.5C>A, XM_017018460.1:c.5C>T, XM_017018460.1:c.5C>A, XR_007062519.1:n.273C>T, XR_007062519.1:n.273C>A, XR_007062518.1:n.125C>T, XR_007062518.1:n.125C>A, XR_007062522.1:n.125C>T, XR_007062522.1:n.125C>A, XM_047427784.1:c.5C>T, XM_047427784.1:c.5C>A, XM_047427783.1:c.5C>T, XM_047427783.1:c.5C>A, XR_007062517.1:n.273C>T, XR_007062517.1:n.273C>A, XR_007062520.1:n.273C>T, XR_007062520.1:n.273C>A, XR_007062521.1:n.125C>T, XR_007062521.1:n.125C>A, NP_149083.2:p.Ala2Val, NP_149083.2:p.Ala2Asp, NP_149084.2:p.Ala2Val, NP_149084.2:p.Ala2Asp, NP_149023.2:p.Ala2Val, NP_149023.2:p.Ala2Asp, XP_006718421.1:p.Ala2Val, XP_006718421.1:p.Ala2Asp, XP_005253240.1:p.Ala2Val, XP_005253240.1:p.Ala2Asp, XP_005253241.1:p.Ala2Val, XP_005253241.1:p.Ala2Asp, XP_011518728.1:p.Ala2Val, XP_011518728.1:p.Ala2Asp, XP_016873952.1:p.Ala2Val, XP_016873952.1:p.Ala2Asp, XP_016873950.1:p.Ala2Val, XP_016873950.1:p.Ala2Asp, XP_016873949.1:p.Ala2Val, XP_016873949.1:p.Ala2Asp, XP_047283740.1:p.Ala2Val, XP_047283740.1:p.Ala2Asp, XP_047283739.1:p.Ala2Val, XP_047283739.1:p.Ala2Asp

Select item 144680930419.

rs1446809304 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5680069 (GRCh38)
11:5701299 (GRCh37)
Canonical SPDI:: NC_000011.10:5680068:C:T
Gene:: TRIM5 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
T=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.5680069C>T, NC_000011.9:g.5701299C>T, NG_029122.1:g.10041G>A, NM_033092.4:c.109G>A, NM_033092.3:c.109G>A, NM_033092.2:c.109G>A, NM_033093.4:c.109G>A, NM_033093.3:c.109G>A, NM_033093.2:c.109G>A, NM_033034.3:c.109G>A, NM_033034.2:c.109G>A, NM_001410958.1:c.109G>A, XM_006718358.4:c.109G>A, XM_006718358.3:c.109G>A, XM_006718358.2:c.109G>A, XM_006718358.1:c.109G>A, XM_005253183.4:c.109G>A, XM_005253183.3:c.109G>A, XM_005253183.2:c.109G>A, XM_005253183.1:c.109G>A, XM_005253184.4:c.109G>A, XM_005253184.3:c.109G>A, XM_005253184.2:c.109G>A, XM_005253184.1:c.109G>A, XM_011520426.4:c.109G>A, XM_011520426.3:c.109G>A, XM_011520426.2:c.109G>A, XM_011520426.1:c.109G>A, XR_001748014.3:n.377G>A, XR_001748014.2:n.387G>A, XR_001748014.1:n.398G>A, XM_017018463.3:c.109G>A, XM_017018461.3:c.109G>A, XM_017018461.2:c.109G>A, XM_017018461.1:c.109G>A, XM_017018460.3:c.109G>A, XM_017018460.2:c.109G>A, XM_017018460.1:c.109G>A, XR_007062519.1:n.377G>A, XR_007062518.1:n.229G>A, XR_007062522.1:n.229G>A, XM_047427784.1:c.109G>A, XM_047427783.1:c.109G>A, XR_007062517.1:n.377G>A, XR_007062520.1:n.377G>A, XR_007062521.1:n.229G>A, NP_149083.2:p.Ala37Thr, NP_149084.2:p.Ala37Thr, NP_149023.2:p.Ala37Thr, XP_006718421.1:p.Ala37Thr, XP_005253240.1:p.Ala37Thr, XP_005253241.1:p.Ala37Thr, XP_011518728.1:p.Ala37Thr, XP_016873952.1:p.Ala37Thr, XP_016873950.1:p.Ala37Thr, XP_016873949.1:p.Ala37Thr, XP_047283740.1:p.Ala37Thr, XP_047283739.1:p.Ala37Thr

Select item 144328657020.

rs1443286570 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:5667972 (GRCh38)
11:5689202 (GRCh37)
Canonical SPDI:: NC_000011.10:5667971:A:G
Gene:: TRIM5 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.5667972A>G, NC_000011.9:g.5689202A>G, NG_029122.1:g.22138T>C, XM_017018460.3:c.872T>C, XM_017018460.2:c.872T>C, XM_017018460.1:c.872T>C, XP_016873949.1:p.Phe291Ser

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