SNP Links for Protein (Select 530395905) - SNP

Links from Protein

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Select item 14909827891.

rs1490982789 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5679916 (GRCh38)
11:5701146 (GRCh37)
Canonical SPDI:: NC_000011.10:5679915:C:T
Gene:: TRIM5 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5679916C>T, NC_000011.9:g.5701146C>T, NG_029122.1:g.10194G>A, NM_033092.4:c.262G>A, NM_033092.3:c.262G>A, NM_033092.2:c.262G>A, NM_033093.4:c.262G>A, NM_033093.3:c.262G>A, NM_033093.2:c.262G>A, NM_033034.3:c.262G>A, NM_033034.2:c.262G>A, NM_001410958.1:c.262G>A, XM_006718358.4:c.262G>A, XM_006718358.3:c.262G>A, XM_006718358.2:c.262G>A, XM_006718358.1:c.262G>A, XM_005253183.4:c.262G>A, XM_005253183.3:c.262G>A, XM_005253183.2:c.262G>A, XM_005253183.1:c.262G>A, XM_005253184.4:c.262G>A, XM_005253184.3:c.262G>A, XM_005253184.2:c.262G>A, XM_005253184.1:c.262G>A, XM_011520426.4:c.262G>A, XM_011520426.3:c.262G>A, XM_011520426.2:c.262G>A, XM_011520426.1:c.262G>A, XR_001748014.3:n.530G>A, XR_001748014.2:n.540G>A, XR_001748014.1:n.551G>A, XM_017018463.3:c.262G>A, XM_017018461.3:c.262G>A, XM_017018461.2:c.262G>A, XM_017018461.1:c.262G>A, XM_017018460.3:c.262G>A, XM_017018460.2:c.262G>A, XM_017018460.1:c.262G>A, XR_007062519.1:n.530G>A, XR_007062518.1:n.382G>A, XR_007062522.1:n.382G>A, XM_047427784.1:c.262G>A, XM_047427783.1:c.262G>A, XR_007062517.1:n.530G>A, XR_007062520.1:n.530G>A, XR_007062521.1:n.382G>A, NP_149083.2:p.Glu88Lys, NP_149084.2:p.Glu88Lys, NP_149023.2:p.Glu88Lys, XP_006718421.1:p.Glu88Lys, XP_005253240.1:p.Glu88Lys, XP_005253241.1:p.Glu88Lys, XP_011518728.1:p.Glu88Lys, XP_016873952.1:p.Glu88Lys, XP_016873950.1:p.Glu88Lys, XP_016873949.1:p.Glu88Lys, XP_047283740.1:p.Glu88Lys, XP_047283739.1:p.Glu88Lys

Select item 14897840532.

rs1489784053 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5678225 (GRCh38)
11:5699455 (GRCh37)
Canonical SPDI:: NC_000011.10:5678224:C:T
Gene:: TRIM5 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000015/4 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.5678225C>T, NC_000011.9:g.5699455C>T, NG_029122.1:g.11885G>A, NM_033092.4:c.723G>A, NM_033092.3:c.723G>A, NM_033092.2:c.723G>A, NM_033093.4:c.723G>A, NM_033093.3:c.723G>A, NM_033093.2:c.723G>A, NM_033034.3:c.723G>A, NM_033034.2:c.723G>A, NM_001410958.1:c.723G>A, XM_006718358.4:c.723G>A, XM_006718358.3:c.723G>A, XM_006718358.2:c.723G>A, XM_006718358.1:c.723G>A, XM_005253183.4:c.723G>A, XM_005253183.3:c.723G>A, XM_005253183.2:c.723G>A, XM_005253183.1:c.723G>A, XM_005253184.4:c.723G>A, XM_005253184.3:c.723G>A, XM_005253184.2:c.723G>A, XM_005253184.1:c.723G>A, XM_011520426.4:c.723G>A, XM_011520426.3:c.723G>A, XM_011520426.2:c.723G>A, XM_011520426.1:c.723G>A, XR_001748014.3:n.991G>A, XR_001748014.2:n.1001G>A, XR_001748014.1:n.1012G>A, XM_017018463.3:c.723G>A, XM_017018461.3:c.723G>A, XM_017018461.2:c.723G>A, XM_017018461.1:c.723G>A, XM_017018460.3:c.723G>A, XM_017018460.2:c.723G>A, XM_017018460.1:c.723G>A, XR_007062519.1:n.991G>A, XR_007062518.1:n.843G>A, XR_007062522.1:n.843G>A, XM_047427784.1:c.723G>A, XM_047427783.1:c.723G>A, XR_007062517.1:n.991G>A, XR_007062520.1:n.991G>A, XR_007062521.1:n.843G>A

Select item 14872554383.

rs1487255438 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5678333 (GRCh38)
11:5699563 (GRCh37)
Canonical SPDI:: NC_000011.10:5678332:C:T
Gene:: TRIM5 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.5678333C>T, NC_000011.9:g.5699563C>T, NG_029122.1:g.11777G>A, NM_033092.4:c.615G>A, NM_033092.3:c.615G>A, NM_033092.2:c.615G>A, NM_033093.4:c.615G>A, NM_033093.3:c.615G>A, NM_033093.2:c.615G>A, NM_033034.3:c.615G>A, NM_033034.2:c.615G>A, NM_001410958.1:c.615G>A, XM_006718358.4:c.615G>A, XM_006718358.3:c.615G>A, XM_006718358.2:c.615G>A, XM_006718358.1:c.615G>A, XM_005253183.4:c.615G>A, XM_005253183.3:c.615G>A, XM_005253183.2:c.615G>A, XM_005253183.1:c.615G>A, XM_005253184.4:c.615G>A, XM_005253184.3:c.615G>A, XM_005253184.2:c.615G>A, XM_005253184.1:c.615G>A, XM_011520426.4:c.615G>A, XM_011520426.3:c.615G>A, XM_011520426.2:c.615G>A, XM_011520426.1:c.615G>A, XR_001748014.3:n.883G>A, XR_001748014.2:n.893G>A, XR_001748014.1:n.904G>A, XM_017018463.3:c.615G>A, XM_017018461.3:c.615G>A, XM_017018461.2:c.615G>A, XM_017018461.1:c.615G>A, XM_017018460.3:c.615G>A, XM_017018460.2:c.615G>A, XM_017018460.1:c.615G>A, XR_007062519.1:n.883G>A, XR_007062518.1:n.735G>A, XR_007062522.1:n.735G>A, XM_047427784.1:c.615G>A, XM_047427783.1:c.615G>A, XR_007062517.1:n.883G>A, XR_007062520.1:n.883G>A, XR_007062521.1:n.735G>A

Select item 14836620004.

rs1483662000 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5678290 (GRCh38)
11:5699520 (GRCh37)
Canonical SPDI:: NC_000011.10:5678289:C:T
Gene:: TRIM5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.5678290C>T, NC_000011.9:g.5699520C>T, NG_029122.1:g.11820G>A, NM_033092.4:c.658G>A, NM_033092.3:c.658G>A, NM_033092.2:c.658G>A, NM_033093.4:c.658G>A, NM_033093.3:c.658G>A, NM_033093.2:c.658G>A, NM_033034.3:c.658G>A, NM_033034.2:c.658G>A, NM_001410958.1:c.658G>A, XM_006718358.4:c.658G>A, XM_006718358.3:c.658G>A, XM_006718358.2:c.658G>A, XM_006718358.1:c.658G>A, XM_005253183.4:c.658G>A, XM_005253183.3:c.658G>A, XM_005253183.2:c.658G>A, XM_005253183.1:c.658G>A, XM_005253184.4:c.658G>A, XM_005253184.3:c.658G>A, XM_005253184.2:c.658G>A, XM_005253184.1:c.658G>A, XM_011520426.4:c.658G>A, XM_011520426.3:c.658G>A, XM_011520426.2:c.658G>A, XM_011520426.1:c.658G>A, XR_001748014.3:n.926G>A, XR_001748014.2:n.936G>A, XR_001748014.1:n.947G>A, XM_017018463.3:c.658G>A, XM_017018461.3:c.658G>A, XM_017018461.2:c.658G>A, XM_017018461.1:c.658G>A, XM_017018460.3:c.658G>A, XM_017018460.2:c.658G>A, XM_017018460.1:c.658G>A, XR_007062519.1:n.926G>A, XR_007062518.1:n.778G>A, XR_007062522.1:n.778G>A, XM_047427784.1:c.658G>A, XM_047427783.1:c.658G>A, XR_007062517.1:n.926G>A, XR_007062520.1:n.926G>A, XR_007062521.1:n.778G>A, NP_149083.2:p.Glu220Lys, NP_149084.2:p.Glu220Lys, NP_149023.2:p.Glu220Lys, XP_006718421.1:p.Glu220Lys, XP_005253240.1:p.Glu220Lys, XP_005253241.1:p.Glu220Lys, XP_011518728.1:p.Glu220Lys, XP_016873952.1:p.Glu220Lys, XP_016873950.1:p.Glu220Lys, XP_016873949.1:p.Glu220Lys, XP_047283740.1:p.Glu220Lys, XP_047283739.1:p.Glu220Lys

Select item 14792289525.

rs1479228952 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5665667 (GRCh38)
11:5686897 (GRCh37)
Canonical SPDI:: NC_000011.10:5665666:C:T
Gene:: TRIM5 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,non_coding_transcript_variant,genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000006/1 (GnomAD_exomes)
T=0.000011/3 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.5665667C>T, NC_000011.9:g.5686897C>T, NG_029122.1:g.24443G>A, NM_033092.4:c.884G>A, NM_033092.3:c.884G>A, NM_033092.2:c.884G>A, NM_033093.4:c.884G>A, NM_033093.3:c.884G>A, NM_033093.2:c.884G>A, NM_033034.3:c.884G>A, NM_033034.2:c.884G>A, NM_001410958.1:c.783G>A, XM_006718358.4:c.783G>A, XM_006718358.3:c.783G>A, XM_006718358.2:c.783G>A, XM_006718358.1:c.783G>A, XM_005253183.4:c.884G>A, XM_005253183.3:c.884G>A, XM_005253183.2:c.884G>A, XM_005253183.1:c.884G>A, XM_005253184.4:c.884G>A, XM_005253184.3:c.884G>A, XM_005253184.2:c.884G>A, XM_005253184.1:c.884G>A, XM_011520426.4:c.783G>A, XM_011520426.3:c.783G>A, XM_011520426.2:c.783G>A, XM_011520426.1:c.783G>A, XR_001748014.3:n.1152G>A, XR_001748014.2:n.1162G>A, XR_001748014.1:n.1173G>A, XM_017018463.3:c.783G>A, XM_017018461.3:c.783G>A, XM_017018461.2:c.783G>A, XM_017018461.1:c.783G>A, NR_002777.3:n.552C>T, NR_002777.2:n.552C>T, XR_007062519.1:n.1129G>A, XR_007062518.1:n.903G>A, XM_047427783.1:c.783G>A, XR_007062517.1:n.1051G>A, NR_002777.1:n.553C>T, NP_149083.2:p.Arg295Gln, NP_149084.2:p.Arg295Gln, NP_149023.2:p.Arg295Gln, XP_005253240.1:p.Arg295Gln, XP_005253241.1:p.Arg295Gln

Select item 14766654786.

rs1476665478 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:5679979 (GRCh38)
11:5701209 (GRCh37)
Canonical SPDI:: NC_000011.10:5679978:T:G
Gene:: TRIM5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.000043/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.5679979T>G, NC_000011.9:g.5701209T>G, NG_029122.1:g.10131A>C, NM_033092.4:c.199A>C, NM_033092.3:c.199A>C, NM_033092.2:c.199A>C, NM_033093.4:c.199A>C, NM_033093.3:c.199A>C, NM_033093.2:c.199A>C, NM_033034.3:c.199A>C, NM_033034.2:c.199A>C, NM_001410958.1:c.199A>C, XM_006718358.4:c.199A>C, XM_006718358.3:c.199A>C, XM_006718358.2:c.199A>C, XM_006718358.1:c.199A>C, XM_005253183.4:c.199A>C, XM_005253183.3:c.199A>C, XM_005253183.2:c.199A>C, XM_005253183.1:c.199A>C, XM_005253184.4:c.199A>C, XM_005253184.3:c.199A>C, XM_005253184.2:c.199A>C, XM_005253184.1:c.199A>C, XM_011520426.4:c.199A>C, XM_011520426.3:c.199A>C, XM_011520426.2:c.199A>C, XM_011520426.1:c.199A>C, XR_001748014.3:n.467A>C, XR_001748014.2:n.477A>C, XR_001748014.1:n.488A>C, XM_017018463.3:c.199A>C, XM_017018461.3:c.199A>C, XM_017018461.2:c.199A>C, XM_017018461.1:c.199A>C, XM_017018460.3:c.199A>C, XM_017018460.2:c.199A>C, XM_017018460.1:c.199A>C, XR_007062519.1:n.467A>C, XR_007062518.1:n.319A>C, XR_007062522.1:n.319A>C, XM_047427784.1:c.199A>C, XM_047427783.1:c.199A>C, XR_007062517.1:n.467A>C, XR_007062520.1:n.467A>C, XR_007062521.1:n.319A>C, NP_149083.2:p.Ile67Leu, NP_149084.2:p.Ile67Leu, NP_149023.2:p.Ile67Leu, XP_006718421.1:p.Ile67Leu, XP_005253240.1:p.Ile67Leu, XP_005253241.1:p.Ile67Leu, XP_011518728.1:p.Ile67Leu, XP_016873952.1:p.Ile67Leu, XP_016873950.1:p.Ile67Leu, XP_016873949.1:p.Ile67Leu, XP_047283740.1:p.Ile67Leu, XP_047283739.1:p.Ile67Leu

Select item 14756831427.

rs1475683142 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:5680109 (GRCh38)
11:5701339 (GRCh37)
Canonical SPDI:: NC_000011.10:5680108: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./0 (ALFA)
C=0.000019/5 (TOPMED)
C=0.000028/7 (GnomAD_exomes)
C=0.000036/5 (GnomAD)
HGVS:: NC_000011.10:g.5680109T>C, NC_000011.9:g.5701339T>C, NG_029122.1:g.10001A>G, NM_033092.4:c.69A>G, NM_033092.3:c.69A>G, NM_033092.2:c.69A>G, NM_033093.4:c.69A>G, NM_033093.3:c.69A>G, NM_033093.2:c.69A>G, NM_033034.3:c.69A>G, NM_033034.2:c.69A>G, NM_001410958.1:c.69A>G, XM_006718358.4:c.69A>G, XM_006718358.3:c.69A>G, XM_006718358.2:c.69A>G, XM_006718358.1:c.69A>G, XM_005253183.4:c.69A>G, XM_005253183.3:c.69A>G, XM_005253183.2:c.69A>G, XM_005253183.1:c.69A>G, XM_005253184.4:c.69A>G, XM_005253184.3:c.69A>G, XM_005253184.2:c.69A>G, XM_005253184.1:c.69A>G, XM_011520426.4:c.69A>G, XM_011520426.3:c.69A>G, XM_011520426.2:c.69A>G, XM_011520426.1:c.69A>G, XR_001748014.3:n.337A>G, XR_001748014.2:n.347A>G, XR_001748014.1:n.358A>G, XM_017018463.3:c.69A>G, XM_017018461.3:c.69A>G, XM_017018461.2:c.69A>G, XM_017018461.1:c.69A>G, XM_017018460.3:c.69A>G, XM_017018460.2:c.69A>G, XM_017018460.1:c.69A>G, XR_007062519.1:n.337A>G, XR_007062518.1:n.189A>G, XR_007062522.1:n.189A>G, XM_047427784.1:c.69A>G, XM_047427783.1:c.69A>G, XR_007062517.1:n.337A>G, XR_007062520.1:n.337A>G, XR_007062521.1:n.189A>G

Select item 14745461218.

rs1474546121 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5678372 (GRCh38)
11:5699602 (GRCh37)
Canonical SPDI:: NC_000011.10:5678371:C:T
Gene:: TRIM5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5678372C>T, NC_000011.9:g.5699602C>T, NG_029122.1:g.11738G>A, NM_033092.4:c.576G>A, NM_033092.3:c.576G>A, NM_033092.2:c.576G>A, NM_033093.4:c.576G>A, NM_033093.3:c.576G>A, NM_033093.2:c.576G>A, NM_033034.3:c.576G>A, NM_033034.2:c.576G>A, NM_001410958.1:c.576G>A, XM_006718358.4:c.576G>A, XM_006718358.3:c.576G>A, XM_006718358.2:c.576G>A, XM_006718358.1:c.576G>A, XM_005253183.4:c.576G>A, XM_005253183.3:c.576G>A, XM_005253183.2:c.576G>A, XM_005253183.1:c.576G>A, XM_005253184.4:c.576G>A, XM_005253184.3:c.576G>A, XM_005253184.2:c.576G>A, XM_005253184.1:c.576G>A, XM_011520426.4:c.576G>A, XM_011520426.3:c.576G>A, XM_011520426.2:c.576G>A, XM_011520426.1:c.576G>A, XR_001748014.3:n.844G>A, XR_001748014.2:n.854G>A, XR_001748014.1:n.865G>A, XM_017018463.3:c.576G>A, XM_017018461.3:c.576G>A, XM_017018461.2:c.576G>A, XM_017018461.1:c.576G>A, XM_017018460.3:c.576G>A, XM_017018460.2:c.576G>A, XM_017018460.1:c.576G>A, XR_007062519.1:n.844G>A, XR_007062518.1:n.696G>A, XR_007062522.1:n.696G>A, XM_047427784.1:c.576G>A, XM_047427783.1:c.576G>A, XR_007062517.1:n.844G>A, XR_007062520.1:n.844G>A, XR_007062521.1:n.696G>A

Select item 14732887799.

rs1473288779 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:5667697 (GRCh38)
11:5688927 (GRCh37)
Canonical SPDI:: NC_000011.10:5667696:G:A
Gene:: TRIM5 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,non_coding_transcript_variant,coding_sequence_variant,downstream_transcript_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5667697G>A, NC_000011.9:g.5688927G>A, NG_029122.1:g.22413C>T, NM_033092.4:c.759C>T, NM_033092.3:c.759C>T, NM_033092.2:c.759C>T, NM_033093.4:c.759C>T, NM_033093.3:c.759C>T, NM_033093.2:c.759C>T, NM_033034.3:c.759C>T, NM_033034.2:c.759C>T, NM_001410958.1:c.759C>T, XM_006718358.4:c.759C>T, XM_006718358.3:c.759C>T, XM_006718358.2:c.759C>T, XM_006718358.1:c.759C>T, XM_005253183.4:c.759C>T, XM_005253183.3:c.759C>T, XM_005253183.2:c.759C>T, XM_005253183.1:c.759C>T, XM_005253184.4:c.759C>T, XM_005253184.3:c.759C>T, XM_005253184.2:c.759C>T, XM_005253184.1:c.759C>T, XM_011520426.4:c.759C>T, XM_011520426.3:c.759C>T, XM_011520426.2:c.759C>T, XM_011520426.1:c.759C>T, XR_001748014.3:n.1027C>T, XR_001748014.2:n.1037C>T, XR_001748014.1:n.1048C>T, XM_017018463.3:c.759C>T, XM_017018461.3:c.759C>T, XM_017018461.2:c.759C>T, XM_017018461.1:c.759C>T, XR_007062518.1:n.879C>T, XM_047427783.1:c.759C>T, XR_007062517.1:n.1027C>T

Select item 147257214810.

rs1472572148 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5680022 (GRCh38)
11:5701252 (GRCh37)
Canonical SPDI:: NC_000011.10:5680021:C:T
Gene:: TRIM5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5680022C>T, NC_000011.9:g.5701252C>T, NG_029122.1:g.10088G>A, NM_033092.4:c.156G>A, NM_033092.3:c.156G>A, NM_033092.2:c.156G>A, NM_033093.4:c.156G>A, NM_033093.3:c.156G>A, NM_033093.2:c.156G>A, NM_033034.3:c.156G>A, NM_033034.2:c.156G>A, NM_001410958.1:c.156G>A, XM_006718358.4:c.156G>A, XM_006718358.3:c.156G>A, XM_006718358.2:c.156G>A, XM_006718358.1:c.156G>A, XM_005253183.4:c.156G>A, XM_005253183.3:c.156G>A, XM_005253183.2:c.156G>A, XM_005253183.1:c.156G>A, XM_005253184.4:c.156G>A, XM_005253184.3:c.156G>A, XM_005253184.2:c.156G>A, XM_005253184.1:c.156G>A, XM_011520426.4:c.156G>A, XM_011520426.3:c.156G>A, XM_011520426.2:c.156G>A, XM_011520426.1:c.156G>A, XR_001748014.3:n.424G>A, XR_001748014.2:n.434G>A, XR_001748014.1:n.445G>A, XM_017018463.3:c.156G>A, XM_017018461.3:c.156G>A, XM_017018461.2:c.156G>A, XM_017018461.1:c.156G>A, XM_017018460.3:c.156G>A, XM_017018460.2:c.156G>A, XM_017018460.1:c.156G>A, XR_007062519.1:n.424G>A, XR_007062518.1:n.276G>A, XR_007062522.1:n.276G>A, XM_047427784.1:c.156G>A, XM_047427783.1:c.156G>A, XR_007062517.1:n.424G>A, XR_007062520.1:n.424G>A, XR_007062521.1:n.276G>A

Select item 147133037811.

rs1471330378 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:5679076 (GRCh38)
11:5700306 (GRCh37)
Canonical SPDI:: NC_000011.10:5679075:T:C
Gene:: TRIM5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000051/1 (ALFA)
C=0.000012/3 (GnomAD_exomes)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.5679076T>C, NC_000011.9:g.5700306T>C, NG_029122.1:g.11034A>G, NM_033092.4:c.511A>G, NM_033092.3:c.511A>G, NM_033092.2:c.511A>G, NM_033093.4:c.511A>G, NM_033093.3:c.511A>G, NM_033093.2:c.511A>G, NM_033034.3:c.511A>G, NM_033034.2:c.511A>G, NM_001410958.1:c.511A>G, XM_006718358.4:c.511A>G, XM_006718358.3:c.511A>G, XM_006718358.2:c.511A>G, XM_006718358.1:c.511A>G, XM_005253183.4:c.511A>G, XM_005253183.3:c.511A>G, XM_005253183.2:c.511A>G, XM_005253183.1:c.511A>G, XM_005253184.4:c.511A>G, XM_005253184.3:c.511A>G, XM_005253184.2:c.511A>G, XM_005253184.1:c.511A>G, XM_011520426.4:c.511A>G, XM_011520426.3:c.511A>G, XM_011520426.2:c.511A>G, XM_011520426.1:c.511A>G, XR_001748014.3:n.779A>G, XR_001748014.2:n.789A>G, XR_001748014.1:n.800A>G, XM_017018463.3:c.511A>G, XM_017018461.3:c.511A>G, XM_017018461.2:c.511A>G, XM_017018461.1:c.511A>G, XM_017018460.3:c.511A>G, XM_017018460.2:c.511A>G, XM_017018460.1:c.511A>G, XR_007062519.1:n.779A>G, XR_007062518.1:n.631A>G, XR_007062522.1:n.631A>G, XM_047427784.1:c.511A>G, XM_047427783.1:c.511A>G, XR_007062517.1:n.779A>G, XR_007062520.1:n.779A>G, XR_007062521.1:n.631A>G, NP_149083.2:p.Lys171Glu, NP_149084.2:p.Lys171Glu, NP_149023.2:p.Lys171Glu, XP_006718421.1:p.Lys171Glu, XP_005253240.1:p.Lys171Glu, XP_005253241.1:p.Lys171Glu, XP_011518728.1:p.Lys171Glu, XP_016873952.1:p.Lys171Glu, XP_016873950.1:p.Lys171Glu, XP_016873949.1:p.Lys171Glu, XP_047283740.1:p.Lys171Glu, XP_047283739.1:p.Lys171Glu

Select item 147130012012.

rs1471300120 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:5664137 (GRCh38)
11:5685367 (GRCh37)
Canonical SPDI:: NC_000011.10:5664136:G:A
Gene:: TRIM5 (Varview)
Functional Consequence:: intron_variant,3_prime_UTR_variant,missense_variant,synonymous_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000008/1 (GnomAD)
A=0.000106/2 (TOMMO)
HGVS:: NC_000011.10:g.5664137G>A, NC_000011.9:g.5685367G>A, NG_029122.1:g.25973C>T, NM_033092.4:c.*1370C>T, NM_033092.3:c.*1370C>T, NM_033092.2:c.*1370C>T, NM_033093.4:c.932C>T, NM_033093.3:c.932C>T, NM_033093.2:c.932C>T, NM_033034.3:c.*672C>T, NM_033034.2:c.*672C>T, NM_001410958.1:c.*1255C>T, XM_006718358.4:c.*1255C>T, XM_006718358.3:c.*1255C>T, XM_006718358.2:c.*1255C>T, XM_005253183.4:c.*672C>T, XM_005253183.3:c.*672C>T, XM_005253183.2:c.*672C>T, XM_005253183.1:c.*672C>T, XM_005253184.4:c.932C>T, XM_005253184.3:c.932C>T, XM_005253184.2:c.932C>T, XM_005253184.1:c.932C>T, XM_011520426.4:c.831C>T, XM_011520426.3:c.831C>T, XM_011520426.2:c.831C>T, XM_011520426.1:c.831C>T, XM_017018463.3:c.*1255C>T, XM_017018461.3:c.831C>T, XM_017018461.2:c.831C>T, XM_017018461.1:c.831C>T, NP_149084.2:p.Thr311Ile, XP_005253241.1:p.Thr311Ile

Select item 146851813013.

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 146684691214.

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 146481570515.

rs1464815705 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:5664095 (GRCh38)
11:5685325 (GRCh37)
Canonical SPDI:: NC_000011.10:5664094:G:T
Gene:: TRIM5 (Varview)
Functional Consequence:: missense_variant,genic_downstream_transcript_variant,synonymous_variant,3_prime_UTR_variant,intron_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.5664095G>T, NC_000011.9:g.5685325G>T, NG_029122.1:g.26015C>A, NM_033092.4:c.*1412C>A, NM_033092.3:c.*1412C>A, NM_033092.2:c.*1412C>A, NM_033093.4:c.974C>A, NM_033093.3:c.974C>A, NM_033093.2:c.974C>A, NM_033034.3:c.*714C>A, NM_033034.2:c.*714C>A, NM_001410958.1:c.*1297C>A, XM_006718358.4:c.*1297C>A, XM_006718358.3:c.*1297C>A, XM_006718358.2:c.*1297C>A, XM_005253183.4:c.*714C>A, XM_005253183.3:c.*714C>A, XM_005253183.2:c.*714C>A, XM_005253183.1:c.*714C>A, XM_005253184.4:c.974C>A, XM_005253184.3:c.974C>A, XM_005253184.2:c.974C>A, XM_005253184.1:c.974C>A, XM_011520426.4:c.873C>A, XM_011520426.3:c.873C>A, XM_011520426.2:c.873C>A, XM_011520426.1:c.873C>A, XM_017018463.3:c.*1297C>A, XM_017018461.3:c.873C>A, XM_017018461.2:c.873C>A, XM_017018461.1:c.873C>A, NP_149084.2:p.Pro325His, XP_005253241.1:p.Pro325His

Select item 146249651216.

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 145793909417.

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 145552824518.

rs1455528245 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:5664142 (GRCh38)
11:5685372 (GRCh37)
Canonical SPDI:: NC_000011.10:5664141:A:G
Gene:: TRIM5 (Varview)
Functional Consequence:: missense_variant,genic_downstream_transcript_variant,synonymous_variant,3_prime_UTR_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.5664142A>G, NC_000011.9:g.5685372A>G, NG_029122.1:g.25968T>C, NM_033092.4:c.*1365T>C, NM_033092.3:c.*1365T>C, NM_033092.2:c.*1365T>C, NM_033093.4:c.927T>C, NM_033093.3:c.927T>C, NM_033093.2:c.927T>C, NM_033034.3:c.*667T>C, NM_033034.2:c.*667T>C, NM_001410958.1:c.*1250T>C, XM_006718358.4:c.*1250T>C, XM_006718358.3:c.*1250T>C, XM_006718358.2:c.*1250T>C, XM_005253183.4:c.*667T>C, XM_005253183.3:c.*667T>C, XM_005253183.2:c.*667T>C, XM_005253183.1:c.*667T>C, XM_005253184.4:c.927T>C, XM_005253184.3:c.927T>C, XM_005253184.2:c.927T>C, XM_005253184.1:c.927T>C, XM_011520426.4:c.826T>C, XM_011520426.3:c.826T>C, XM_011520426.2:c.826T>C, XM_011520426.1:c.826T>C, XM_017018463.3:c.*1250T>C, XM_017018461.3:c.826T>C, XM_017018461.2:c.826T>C, XM_017018461.1:c.826T>C, XP_011518728.1:p.Cys276Arg, XP_016873950.1:p.Cys276Arg

Select item 144843004119.

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 144730393220.

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

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