SNP Links for Protein (Select 952556270) - SNP

Links from Protein

Items: 1 to 20 of 74

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Select item 14886745761.

rs1488674576 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:149970062 (GRCh38)
6:150291198 (GRCh37)
Canonical SPDI:: NC_000006.12:149970061:C:T
Gene:: ULBP1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.149970062C>T, NC_000006.11:g.150291198C>T, NM_025218.4:c.672C>T, NM_025218.3:c.672C>T, NM_025218.2:c.672C>T, NR_133659.2:n.2127C>T, NR_133659.1:n.2096C>T, NM_001317089.2:c.132C>T, NM_001317089.1:c.132C>T

Select item 14844605272.

rs1484460527 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 6:149964071 (GRCh38)
6:150285207 (GRCh37)
Canonical SPDI:: NC_000006.12:149964070:G:A,NC_000006.12:149964070:G:T
Gene:: ULBP1 (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 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.00006/1 (TOMMO)
HGVS:: NC_000006.12:g.149964071G>A, NC_000006.12:g.149964071G>T, NC_000006.11:g.150285207G>A, NC_000006.11:g.150285207G>T, NM_025218.4:c.22G>A, NM_025218.4:c.22G>T, NM_025218.3:c.22G>A, NM_025218.3:c.22G>T, NM_025218.2:c.22G>A, NM_025218.2:c.22G>T, NR_133659.2:n.129G>A, NR_133659.2:n.129G>T, NR_133659.1:n.98G>A, NR_133659.1:n.98G>T, XM_017011322.2:c.22G>A, XM_017011322.2:c.22G>T, XM_017011322.1:c.22G>A, XM_017011322.1:c.22G>T, NM_001317089.2:c.22G>A, NM_001317089.2:c.22G>T, NM_001317089.1:c.22G>A, NM_001317089.1:c.22G>T, NP_079494.1:p.Ala8Thr, NP_079494.1:p.Ala8Ser, XP_016866811.1:p.Ala8Thr, XP_016866811.1:p.Ala8Ser, NP_001304018.1:p.Ala8Thr, NP_001304018.1:p.Ala8Ser

Select item 14676199143.

rs1467619914 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:149964124 (GRCh38)
6:150285260 (GRCh37)
Canonical SPDI:: NC_000006.12:149964123:A:G
Gene:: ULBP1 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.149964124A>G, NC_000006.11:g.150285260A>G, NM_025218.4:c.75A>G, NM_025218.3:c.75A>G, NM_025218.2:c.75A>G, NR_133659.2:n.182A>G, NR_133659.1:n.151A>G, XM_017011322.2:c.75A>G, XM_017011322.1:c.75A>G, NM_001317089.2:c.75A>G, NM_001317089.1:c.75A>G

Select item 14571147424.

rs1457114742 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:149964106 (GRCh38)
6:150285242 (GRCh37)
Canonical SPDI:: NC_000006.12:149964105:G:A
Gene:: ULBP1 (Varview)
Functional Consequence:: synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.149964106G>A, NC_000006.11:g.150285242G>A, NM_025218.4:c.57G>A, NM_025218.3:c.57G>A, NM_025218.2:c.57G>A, NR_133659.2:n.164G>A, NR_133659.1:n.133G>A, XM_017011322.2:c.57G>A, XM_017011322.1:c.57G>A, NM_001317089.2:c.57G>A, NM_001317089.1:c.57G>A

Select item 14264431275.

rs1426443127 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 6:149970068 (GRCh38)
6:150291204 (GRCh37)
Canonical SPDI:: NC_000006.12:149970067:C:A,NC_000006.12:149970067:C:T
Gene:: ULBP1 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,synonymous_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (GnomAD)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000006.12:g.149970068C>A, NC_000006.12:g.149970068C>T, NC_000006.11:g.150291204C>A, NC_000006.11:g.150291204C>T, NM_025218.4:c.678C>A, NM_025218.4:c.678C>T, NM_025218.3:c.678C>A, NM_025218.3:c.678C>T, NM_025218.2:c.678C>A, NM_025218.2:c.678C>T, NR_133659.2:n.2133C>A, NR_133659.2:n.2133C>T, NR_133659.1:n.2102C>A, NR_133659.1:n.2102C>T, NM_001317089.2:c.138C>A, NM_001317089.2:c.138C>T, NM_001317089.1:c.138C>A, NM_001317089.1:c.138C>T

Select item 14237824876.

rs1423782487 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:149964123 (GRCh38)
6:150285259 (GRCh37)
Canonical SPDI:: NC_000006.12:149964122:C:A
Gene:: ULBP1 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
HGVS:: NC_000006.12:g.149964123C>A, NC_000006.11:g.150285259C>A, NM_025218.4:c.74C>A, NM_025218.3:c.74C>A, NM_025218.2:c.74C>A, NR_133659.2:n.181C>A, NR_133659.1:n.150C>A, XM_017011322.2:c.74C>A, XM_017011322.1:c.74C>A, NM_001317089.2:c.74C>A, NM_001317089.1:c.74C>A, NP_079494.1:p.Ala25Glu, XP_016866811.1:p.Ala25Glu, NP_001304018.1:p.Ala25Glu

Select item 14122079307.

rs1412207930 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:149964053 (GRCh38)
6:150285189 (GRCh37)
Canonical SPDI:: NC_000006.12:149964052:G:A
Gene:: ULBP1 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.149964053G>A, NC_000006.11:g.150285189G>A, NM_025218.4:c.4G>A, NM_025218.3:c.4G>A, NM_025218.2:c.4G>A, NR_133659.2:n.111G>A, NR_133659.1:n.80G>A, XM_017011322.2:c.4G>A, XM_017011322.1:c.4G>A, NM_001317089.2:c.4G>A, NM_001317089.1:c.4G>A, NP_079494.1:p.Ala2Thr, XP_016866811.1:p.Ala2Thr, NP_001304018.1:p.Ala2Thr

Select item 14012456438.

rs1401245643 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:149970066 (GRCh38)
6:150291202 (GRCh37)
Canonical SPDI:: NC_000006.12:149970065:A:G
Gene:: ULBP1 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant,non_coding_transcript_variant
HGVS:: NC_000006.12:g.149970066A>G, NC_000006.11:g.150291202A>G, NM_025218.4:c.676A>G, NM_025218.3:c.676A>G, NM_025218.2:c.676A>G, NR_133659.2:n.2131A>G, NR_133659.1:n.2100A>G, NM_001317089.2:c.136A>G, NM_001317089.1:c.136A>G, NP_079494.1:p.Thr226Ala, NP_001304018.1:p.Thr46Ala

Select item 13968607869.

rs1396860786 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 6:149970122 (GRCh38)
6:150291258 (GRCh37)
Canonical SPDI:: NC_000006.12:149970121:A:T
Gene:: ULBP1 (Varview)
Functional Consequence:: intron_variant,missense_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)
HGVS:: NC_000006.12:g.149970122A>T, NC_000006.11:g.150291258A>T, NM_025218.4:c.732A>T, NM_025218.3:c.732A>T, NM_025218.2:c.732A>T, NR_133659.2:n.2187A>T, NR_133659.1:n.2156A>T, NM_001317089.2:c.192A>T, NM_001317089.1:c.192A>T, NP_079494.1:p.Arg244Ser, NP_001304018.1:p.Arg64Ser

Select item 138201043010.

rs1382010430 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:149970101 (GRCh38)
6:150291237 (GRCh37)
Canonical SPDI:: NC_000006.12:149970100:C:T
Gene:: ULBP1 (Varview)
Functional Consequence:: synonymous_variant,non_coding_transcript_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.149970101C>T, NC_000006.11:g.150291237C>T, NM_025218.4:c.711C>T, NM_025218.3:c.711C>T, NM_025218.2:c.711C>T, NR_133659.2:n.2166C>T, NR_133659.1:n.2135C>T, NM_001317089.2:c.171C>T, NM_001317089.1:c.171C>T

Select item 136436565311.

rs1364365653 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:149970086 (GRCh38)
6:150291222 (GRCh37)
Canonical SPDI:: NC_000006.12:149970085:T:C
Gene:: ULBP1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,intron_variant,non_coding_transcript_variant
HGVS:: NC_000006.12:g.149970086T>C, NC_000006.11:g.150291222T>C, NM_025218.4:c.696T>C, NM_025218.3:c.696T>C, NM_025218.2:c.696T>C, NR_133659.2:n.2151T>C, NR_133659.1:n.2120T>C, NM_001317089.2:c.156T>C, NM_001317089.1:c.156T>C

Select item 135601841512.

rs1356018415 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 6:149970024 (GRCh38)
6:150291160 (GRCh37)
Canonical SPDI:: NC_000006.12:149970023:T:A,NC_000006.12:149970023:T:G
Gene:: ULBP1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.149970024T>A, NC_000006.12:g.149970024T>G, NC_000006.11:g.150291160T>A, NC_000006.11:g.150291160T>G, NM_025218.4:c.634T>A, NM_025218.4:c.634T>G, NM_025218.3:c.634T>A, NM_025218.3:c.634T>G, NM_025218.2:c.634T>A, NM_025218.2:c.634T>G, NR_133659.2:n.2089T>A, NR_133659.2:n.2089T>G, NR_133659.1:n.2058T>A, NR_133659.1:n.2058T>G, NM_001317089.2:c.94T>A, NM_001317089.2:c.94T>G, NM_001317089.1:c.94T>A, NM_001317089.1:c.94T>G, NP_079494.1:p.Ser212Thr, NP_079494.1:p.Ser212Ala, NP_001304018.1:p.Ser32Thr, NP_001304018.1:p.Ser32Ala

Select item 134540719113.

rs1345407191 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:149970042 (GRCh38)
6:150291178 (GRCh37)
Canonical SPDI:: NC_000006.12:149970041:A:G
Gene:: ULBP1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.149970042A>G, NC_000006.11:g.150291178A>G, NM_025218.4:c.652A>G, NM_025218.3:c.652A>G, NM_025218.2:c.652A>G, NR_133659.2:n.2107A>G, NR_133659.1:n.2076A>G, NM_001317089.2:c.112A>G, NM_001317089.1:c.112A>G, NP_079494.1:p.Thr218Ala, NP_001304018.1:p.Thr38Ala

Select item 132348172714.

rs1323481727 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 6:149964068 (GRCh38)
6:150285204 (GRCh37)
Canonical SPDI:: NC_000006.12:149964067:C:G,NC_000006.12:149964067:C:T
Gene:: ULBP1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.149964068C>G, NC_000006.12:g.149964068C>T, NC_000006.11:g.150285204C>G, NC_000006.11:g.150285204C>T, NM_025218.4:c.19C>G, NM_025218.4:c.19C>T, NM_025218.3:c.19C>G, NM_025218.3:c.19C>T, NM_025218.2:c.19C>G, NM_025218.2:c.19C>T, NR_133659.2:n.126C>G, NR_133659.2:n.126C>T, NR_133659.1:n.95C>G, NR_133659.1:n.95C>T, XM_017011322.2:c.19C>G, XM_017011322.2:c.19C>T, XM_017011322.1:c.19C>G, XM_017011322.1:c.19C>T, NM_001317089.2:c.19C>G, NM_001317089.2:c.19C>T, NM_001317089.1:c.19C>G, NM_001317089.1:c.19C>T, NP_079494.1:p.Pro7Ala, NP_079494.1:p.Pro7Ser, XP_016866811.1:p.Pro7Ala, XP_016866811.1:p.Pro7Ser, NP_001304018.1:p.Pro7Ala, NP_001304018.1:p.Pro7Ser

Select item 130607912515.

rs1306079125 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 6:149970046 (GRCh38)
6:150291182 (GRCh37)
Canonical SPDI:: NC_000006.12:149970045:A:C
Gene:: ULBP1 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000094/2 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.149970046A>C, NC_000006.11:g.150291182A>C, NM_025218.4:c.656A>C, NM_025218.3:c.656A>C, NM_025218.2:c.656A>C, NR_133659.2:n.2111A>C, NR_133659.1:n.2080A>C, NM_001317089.2:c.116A>C, NM_001317089.1:c.116A>C, NP_079494.1:p.Gln219Pro, NP_001304018.1:p.Gln39Pro

Select item 124964758316.

rs1249647583 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:149970056 (GRCh38)
6:150291192 (GRCh37)
Canonical SPDI:: NC_000006.12:149970055:C:G
Gene:: ULBP1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.149970056C>G, NC_000006.11:g.150291192C>G, NM_025218.4:c.666C>G, NM_025218.3:c.666C>G, NM_025218.2:c.666C>G, NR_133659.2:n.2121C>G, NR_133659.1:n.2090C>G, NM_001317089.2:c.126C>G, NM_001317089.1:c.126C>G

Select item 124802464917.

rs1248024649 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:149964114 (GRCh38)
6:150285250 (GRCh37)
Canonical SPDI:: NC_000006.12:149964113:G:T
Gene:: ULBP1 (Varview)
Functional Consequence:: non_coding_transcript_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_000006.12:g.149964114G>T, NC_000006.11:g.150285250G>T, NM_025218.4:c.65G>T, NM_025218.3:c.65G>T, NM_025218.2:c.65G>T, NR_133659.2:n.172G>T, NR_133659.1:n.141G>T, XM_017011322.2:c.65G>T, XM_017011322.1:c.65G>T, NM_001317089.2:c.65G>T, NM_001317089.1:c.65G>T, NP_079494.1:p.Trp22Leu, XP_016866811.1:p.Trp22Leu, NP_001304018.1:p.Trp22Leu

Select item 122033664418.

rs1220336644 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:149970060 (GRCh38)
6:150291196 (GRCh37)
Canonical SPDI:: NC_000006.12:149970059:G:A
Gene:: ULBP1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000006.12:g.149970060G>A, NC_000006.11:g.150291196G>A, NM_025218.4:c.670G>A, NM_025218.3:c.670G>A, NM_025218.2:c.670G>A, NR_133659.2:n.2125G>A, NR_133659.1:n.2094G>A, NM_001317089.2:c.130G>A, NM_001317089.1:c.130G>A, NP_079494.1:p.Ala224Thr, NP_001304018.1:p.Ala44Thr

Select item 121982701819.

rs1219827018 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 6:149970044 (GRCh38)
6:150291180 (GRCh37)
Canonical SPDI:: NC_000006.12:149970043:C:A,NC_000006.12:149970043:C:T
Gene:: ULBP1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000006.12:g.149970044C>A, NC_000006.12:g.149970044C>T, NC_000006.11:g.150291180C>A, NC_000006.11:g.150291180C>T, NM_025218.4:c.654C>A, NM_025218.4:c.654C>T, NM_025218.3:c.654C>A, NM_025218.3:c.654C>T, NM_025218.2:c.654C>A, NM_025218.2:c.654C>T, NR_133659.2:n.2109C>A, NR_133659.2:n.2109C>T, NR_133659.1:n.2078C>A, NR_133659.1:n.2078C>T, NM_001317089.2:c.114C>A, NM_001317089.2:c.114C>T, NM_001317089.1:c.114C>A, NM_001317089.1:c.114C>T

Select item 121865337420.

rs1218653374 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:149964085 (GRCh38)
6:150285221 (GRCh37)
Canonical SPDI:: NC_000006.12:149964084:C:A
Gene:: ULBP1 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained,non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.149964085C>A, NC_000006.11:g.150285221C>A, NM_025218.4:c.36C>A, NM_025218.3:c.36C>A, NM_025218.2:c.36C>A, NR_133659.2:n.143C>A, NR_133659.1:n.112C>A, XM_017011322.2:c.36C>A, XM_017011322.1:c.36C>A, NM_001317089.2:c.36C>A, NM_001317089.1:c.36C>A, NP_079494.1:p.Cys12Ter, XP_016866811.1:p.Cys12Ter, NP_001304018.1:p.Cys12Ter

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