SNP Links for Nucleotide (Select 433660867) - SNP

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Select item 14915805061.

rs1491580506 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 15:64154957 (GRCh38)
15:64447157 (GRCh37)
Canonical SPDI:: NC_000015.10:64154957::C
Gene:: SNX22 (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.00008/1 (ALFA)
HGVS:: NC_000015.10:g.64154957_64154958insC, NC_000015.9:g.64447156_64447157insC, NG_012979.1:g.13198_13199insG, NG_033071.1:g.8241_8242insC, NM_024798.3:c.*449_*450insC, NM_024798.2:c.*449_*450insC, NR_073534.2:n.1123_1124insC, NR_073534.1:n.1137_1138insC, XM_017022581.2:c.*449_*450insC, XM_017022581.1:c.*449_*450insC

Select item 14915049082.

rs1491504908 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 15:64153483 (GRCh38)
15:64445682 (GRCh37)
Canonical SPDI:: NC_000015.10:64153482:CT:
Gene:: SNX22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.64153483_64153484del, NC_000015.9:g.64445682_64445683del, NG_033071.1:g.6767_6768del

Select item 14914289173.

rs1491428917 has merged into rs1403969301 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>-,TT [Show Flanks]
Chromosome:: 15:64153484 (GRCh38)
15:64445683 (GRCh37)
Canonical SPDI:: NC_000015.10:64153483:TTTTTTTT:TTTTTTT,NC_000015.10:64153483:TTTTTTTT:TTTTTTTTT
Gene:: SNX22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.00007/2 (TOMMO)
HGVS:: NC_000015.10:g.64153491del, NC_000015.10:g.64153491dup, NC_000015.9:g.64445690del, NC_000015.9:g.64445690dup, NG_033071.1:g.6775del, NG_033071.1:g.6775dup

Select item 14912357964.

rs1491235796 has merged into rs759317254 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 15:64154967 (GRCh38)
15:64447166 (GRCh37)
Canonical SPDI:: NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000015.10:64154956:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: SNX22 (Varview)
Functional Consequence:: 3_prime_UTR_variant,non_coding_transcript_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
T=0.45/18 (GENOME_DK)
HGVS:: NC_000015.10:g.64154967_64154980del, NC_000015.10:g.64154968_64154980del, NC_000015.10:g.64154969_64154980del, NC_000015.10:g.64154970_64154980del, NC_000015.10:g.64154971_64154980del, NC_000015.10:g.64154972_64154980del, NC_000015.10:g.64154973_64154980del, NC_000015.10:g.64154974_64154980del, NC_000015.10:g.64154975_64154980del, NC_000015.10:g.64154976_64154980del, NC_000015.10:g.64154977_64154980del, NC_000015.10:g.64154978_64154980del, NC_000015.10:g.64154979_64154980del, NC_000015.10:g.64154980del, NC_000015.10:g.64154980dup, NC_000015.10:g.64154979_64154980dup, NC_000015.10:g.64154978_64154980dup, NC_000015.10:g.64154977_64154980dup, NC_000015.10:g.64154976_64154980dup, NC_000015.10:g.64154975_64154980dup, NC_000015.10:g.64154974_64154980dup, NC_000015.10:g.64154973_64154980dup, NC_000015.10:g.64154972_64154980dup, NC_000015.9:g.64447166_64447179del, NC_000015.9:g.64447167_64447179del, NC_000015.9:g.64447168_64447179del, NC_000015.9:g.64447169_64447179del, NC_000015.9:g.64447170_64447179del, NC_000015.9:g.64447171_64447179del, NC_000015.9:g.64447172_64447179del, NC_000015.9:g.64447173_64447179del, NC_000015.9:g.64447174_64447179del, NC_000015.9:g.64447175_64447179del, NC_000015.9:g.64447176_64447179del, NC_000015.9:g.64447177_64447179del, NC_000015.9:g.64447178_64447179del, NC_000015.9:g.64447179del, NC_000015.9:g.64447179dup, NC_000015.9:g.64447178_64447179dup, NC_000015.9:g.64447177_64447179dup, NC_000015.9:g.64447176_64447179dup, NC_000015.9:g.64447175_64447179dup, NC_000015.9:g.64447174_64447179dup, NC_000015.9:g.64447173_64447179dup, NC_000015.9:g.64447172_64447179dup, NC_000015.9:g.64447171_64447179dup, NG_012979.1:g.13186_13199del, NG_012979.1:g.13187_13199del, NG_012979.1:g.13188_13199del, NG_012979.1:g.13189_13199del, NG_012979.1:g.13190_13199del, NG_012979.1:g.13191_13199del, NG_012979.1:g.13192_13199del, NG_012979.1:g.13193_13199del, NG_012979.1:g.13194_13199del, NG_012979.1:g.13195_13199del, NG_012979.1:g.13196_13199del, NG_012979.1:g.13197_13199del, NG_012979.1:g.13198_13199del, NG_012979.1:g.13199del, NG_012979.1:g.13199dup, NG_012979.1:g.13198_13199dup, NG_012979.1:g.13197_13199dup, NG_012979.1:g.13196_13199dup, NG_012979.1:g.13195_13199dup, NG_012979.1:g.13194_13199dup, NG_012979.1:g.13193_13199dup, NG_012979.1:g.13192_13199dup, NG_012979.1:g.13191_13199dup, NG_033071.1:g.8251_8264del, NG_033071.1:g.8252_8264del, NG_033071.1:g.8253_8264del, NG_033071.1:g.8254_8264del, NG_033071.1:g.8255_8264del, NG_033071.1:g.8256_8264del, NG_033071.1:g.8257_8264del, NG_033071.1:g.8258_8264del, NG_033071.1:g.8259_8264del, NG_033071.1:g.8260_8264del, NG_033071.1:g.8261_8264del, NG_033071.1:g.8262_8264del, NG_033071.1:g.8263_8264del, NG_033071.1:g.8264del, NG_033071.1:g.8264dup, NG_033071.1:g.8263_8264dup, NG_033071.1:g.8262_8264dup, NG_033071.1:g.8261_8264dup, NG_033071.1:g.8260_8264dup, NG_033071.1:g.8259_8264dup, NG_033071.1:g.8258_8264dup, NG_033071.1:g.8257_8264dup, NG_033071.1:g.8256_8264dup, NM_024798.3:c.*459_*472del, NM_024798.3:c.*460_*472del, NM_024798.3:c.*461_*472del, NM_024798.3:c.*462_*472del, NM_024798.3:c.*463_*472del, NM_024798.3:c.*464_*472del, NM_024798.3:c.*465_*472del, NM_024798.3:c.*466_*472del, NM_024798.3:c.*467_*472del, NM_024798.3:c.*468_*472del, NM_024798.3:c.*469_*472del, NM_024798.3:c.*470_*472del, NM_024798.3:c.*471_*472del, NM_024798.3:c.*472del, NM_024798.3:c.*472dup, NM_024798.3:c.*471_*472dup, NM_024798.3:c.*470_*472dup, NM_024798.3:c.*469_*472dup, NM_024798.3:c.*468_*472dup, NM_024798.3:c.*467_*472dup, NM_024798.3:c.*466_*472dup, NM_024798.3:c.*465_*472dup, NM_024798.3:c.*464_*472dup, NM_024798.2:c.*459_*472del, NM_024798.2:c.*460_*472del, NM_024798.2:c.*461_*472del, NM_024798.2:c.*462_*472del, NM_024798.2:c.*463_*472del, NM_024798.2:c.*464_*472del, NM_024798.2:c.*465_*472del, NM_024798.2:c.*466_*472del, NM_024798.2:c.*467_*472del, NM_024798.2:c.*468_*472del, NM_024798.2:c.*469_*472del, NM_024798.2:c.*470_*472del, NM_024798.2:c.*471_*472del, NM_024798.2:c.*472del, NM_024798.2:c.*472dup, NM_024798.2:c.*471_*472dup, NM_024798.2:c.*470_*472dup, NM_024798.2:c.*469_*472dup, NM_024798.2:c.*468_*472dup, NM_024798.2:c.*467_*472dup, NM_024798.2:c.*466_*472dup, NM_024798.2:c.*465_*472dup, NM_024798.2:c.*464_*472dup, NR_073534.2:n.1133_1146del, NR_073534.2:n.1134_1146del, NR_073534.2:n.1135_1146del, NR_073534.2:n.1136_1146del, NR_073534.2:n.1137_1146del, NR_073534.2:n.1138_1146del, NR_073534.2:n.1139_1146del, NR_073534.2:n.1140_1146del, NR_073534.2:n.1141_1146del, NR_073534.2:n.1142_1146del, NR_073534.2:n.1143_1146del, NR_073534.2:n.1144_1146del, NR_073534.2:n.1145_1146del, NR_073534.2:n.1146del, NR_073534.2:n.1146dup, NR_073534.2:n.1145_1146dup, NR_073534.2:n.1144_1146dup, NR_073534.2:n.1143_1146dup, NR_073534.2:n.1142_1146dup, NR_073534.2:n.1141_1146dup, NR_073534.2:n.1140_1146dup, NR_073534.2:n.1139_1146dup, NR_073534.2:n.1138_1146dup, NR_073534.1:n.1147_1160del, NR_073534.1:n.1148_1160del, NR_073534.1:n.1149_1160del, NR_073534.1:n.1150_1160del, NR_073534.1:n.1151_1160del, NR_073534.1:n.1152_1160del, NR_073534.1:n.1153_1160del, NR_073534.1:n.1154_1160del, NR_073534.1:n.1155_1160del, NR_073534.1:n.1156_1160del, NR_073534.1:n.1157_1160del, NR_073534.1:n.1158_1160del, NR_073534.1:n.1159_1160del, NR_073534.1:n.1160del, NR_073534.1:n.1160dup, NR_073534.1:n.1159_1160dup, NR_073534.1:n.1158_1160dup, NR_073534.1:n.1157_1160dup, NR_073534.1:n.1156_1160dup, NR_073534.1:n.1155_1160dup, NR_073534.1:n.1154_1160dup, NR_073534.1:n.1153_1160dup, NR_073534.1:n.1152_1160dup, XM_017022581.2:c.*459_*472del, XM_017022581.2:c.*460_*472del, XM_017022581.2:c.*461_*472del, XM_017022581.2:c.*462_*472del, XM_017022581.2:c.*463_*472del, XM_017022581.2:c.*464_*472del, XM_017022581.2:c.*465_*472del, XM_017022581.2:c.*466_*472del, XM_017022581.2:c.*467_*472del, XM_017022581.2:c.*468_*472del, XM_017022581.2:c.*469_*472del, XM_017022581.2:c.*470_*472del, XM_017022581.2:c.*471_*472del, XM_017022581.2:c.*472del, XM_017022581.2:c.*472dup, XM_017022581.2:c.*471_*472dup, XM_017022581.2:c.*470_*472dup, XM_017022581.2:c.*469_*472dup, XM_017022581.2:c.*468_*472dup, XM_017022581.2:c.*467_*472dup, XM_017022581.2:c.*466_*472dup, XM_017022581.2:c.*465_*472dup, XM_017022581.2:c.*464_*472dup, XM_017022581.1:c.*459_*472del, XM_017022581.1:c.*460_*472del, XM_017022581.1:c.*461_*472del, XM_017022581.1:c.*462_*472del, XM_017022581.1:c.*463_*472del, XM_017022581.1:c.*464_*472del, XM_017022581.1:c.*465_*472del, XM_017022581.1:c.*466_*472del, XM_017022581.1:c.*467_*472del, XM_017022581.1:c.*468_*472del, XM_017022581.1:c.*469_*472del, XM_017022581.1:c.*470_*472del, XM_017022581.1:c.*471_*472del, XM_017022581.1:c.*472del, XM_017022581.1:c.*472dup, XM_017022581.1:c.*471_*472dup, XM_017022581.1:c.*470_*472dup, XM_017022581.1:c.*469_*472dup, XM_017022581.1:c.*468_*472dup, XM_017022581.1:c.*467_*472dup, XM_017022581.1:c.*466_*472dup, XM_017022581.1:c.*465_*472dup, XM_017022581.1:c.*464_*472dup

Select item 14909109075.

rs1490910907 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:64158758 (GRCh38)
15:64450957 (GRCh37)
Canonical SPDI:: NC_000015.10:64158757:T:C
Gene:: PPIB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.64158758T>C, NC_000015.9:g.64450957T>C, NG_012979.1:g.9398A>G, NG_033071.1:g.12042T>C

Select item 14909106156.

rs1490910615 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 15:64152364 (GRCh38)
15:64444563 (GRCh37)
Canonical SPDI:: NC_000015.10:64152363:C:A,NC_000015.10:64152363:C:T
Gene:: SNX22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.64152364C>A, NC_000015.10:g.64152364C>T, NC_000015.9:g.64444563C>A, NC_000015.9:g.64444563C>T, NG_033071.1:g.5648C>A, NG_033071.1:g.5648C>T

Select item 14908186667.

rs1490818666 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:64152549 (GRCh38)
15:64444748 (GRCh37)
Canonical SPDI:: NC_000015.10:64152548:C:T
Gene:: SNX22 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000015.10:g.64152549C>T, NC_000015.9:g.64444748C>T, NG_033071.1:g.5833C>T

Select item 14904197408.

rs1490419740 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:64158229 (GRCh38)
15:64450428 (GRCh37)
Canonical SPDI:: NC_000015.10:64158228:T:C
Gene:: PPIB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.64158229T>C, NC_000015.9:g.64450428T>C, NG_012979.1:g.9927A>G, NG_033071.1:g.11513T>C

Select item 14904067359.

rs1490406735 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:64156231 (GRCh38)
15:64448430 (GRCh37)
Canonical SPDI:: NC_000015.10:64156230:G:A
Gene:: PPIB (Varview), SNX22 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant,intron_variant,non_coding_transcript_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_000015.10:g.64156231G>A, NC_000015.9:g.64448430G>A, NG_012979.1:g.11925C>T, NG_033071.1:g.9515G>A, NM_024798.3:c.*1723G>A, NM_024798.2:c.*1723G>A, NR_073534.2:n.2397G>A, NR_073534.1:n.2411G>A, XM_017022581.2:c.*1723G>A, XM_017022581.1:c.*1723G>A

Select item 149008430110.

rs1490084301 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:64158355 (GRCh38)
15:64450554 (GRCh37)
Canonical SPDI:: NC_000015.10:64158354:T:G
Gene:: PPIB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.64158355T>G, NC_000015.9:g.64450554T>G, NG_012979.1:g.9801A>C, NG_033071.1:g.11639T>G

Select item 149007059111.

rs1490070591 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:64159179 (GRCh38)
15:64451378 (GRCh37)
Canonical SPDI:: NC_000015.10:64159178:G:A
Gene:: PPIB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.64159179G>A, NC_000015.9:g.64451378G>A, NG_012979.1:g.8977C>T, NG_033071.1:g.12463G>A

Select item 148960732712.

rs1489607327 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:64152093 (GRCh38)
15:64444292 (GRCh37)
Canonical SPDI:: NC_000015.10:64152092:C:A
Gene:: SNX22 (Varview)
Functional Consequence:: intron_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_000015.10:g.64152093C>A, NC_000015.9:g.64444292C>A, NG_033071.1:g.5377C>A

Select item 148952063213.

rs1489520632 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:64150756 (GRCh38)
15:64442955 (GRCh37)
Canonical SPDI:: NC_000015.10:64150755:C:T
Gene:: SNX22 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.64150756C>T, NC_000015.9:g.64442955C>T, NG_033071.1:g.4040C>T

Select item 148928599414.

rs1489285994 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:64151823 (GRCh38)
15:64444022 (GRCh37)
Canonical SPDI:: NC_000015.10:64151822:C:T
Gene:: SNX22 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000015.10:g.64151823C>T, NC_000015.9:g.64444022C>T, NG_033071.1:g.5107C>T, NM_024798.3:c.48C>T, NM_024798.2:c.48C>T, NR_073534.2:n.93C>T, NR_073534.1:n.107C>T, XM_005254677.4:c.48C>T, XM_005254677.3:c.48C>T, XM_005254677.2:c.48C>T, XM_005254677.1:c.48C>T, XM_017022581.2:c.48C>T, XM_017022581.1:c.48C>T

Select item 148921565815.

rs1489215658 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 15:64151509 (GRCh38)
15:64443708 (GRCh37)
Canonical SPDI:: NC_000015.10:64151508:C:A,NC_000015.10:64151508:C:T
Gene:: SNX22 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00007/1 (ALFA)
HGVS:: NC_000015.10:g.64151509C>A, NC_000015.10:g.64151509C>T, NC_000015.9:g.64443708C>A, NC_000015.9:g.64443708C>T, NG_033071.1:g.4793C>A, NG_033071.1:g.4793C>T

Select item 148912951416.

rs1489129514 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 15:64156216 (GRCh38)
15:64448415 (GRCh37)
Canonical SPDI:: NC_000015.10:64156215:G:A,NC_000015.10:64156215:G:C
Gene:: PPIB (Varview), SNX22 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.64156216G>A, NC_000015.10:g.64156216G>C, NC_000015.9:g.64448415G>A, NC_000015.9:g.64448415G>C, NG_012979.1:g.11940C>T, NG_012979.1:g.11940C>G, NG_033071.1:g.9500G>A, NG_033071.1:g.9500G>C, NM_024798.3:c.*1708G>A, NM_024798.3:c.*1708G>C, NM_024798.2:c.*1708G>A, NM_024798.2:c.*1708G>C, NR_073534.2:n.2382G>A, NR_073534.2:n.2382G>C, NR_073534.1:n.2396G>A, NR_073534.1:n.2396G>C, XM_017022581.2:c.*1708G>A, XM_017022581.2:c.*1708G>C, XM_017022581.1:c.*1708G>A, XM_017022581.1:c.*1708G>C

Select item 148907717217.

rs1489077172 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:64157333 (GRCh38)
15:64449532 (GRCh37)
Canonical SPDI:: NC_000015.10:64157332:G:A
Gene:: PPIB (Varview), SNX22 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.64157333G>A, NC_000015.9:g.64449532G>A, NG_012979.1:g.10823C>T, NG_033071.1:g.10617G>A, NM_024798.3:c.*2825G>A, NM_024798.2:c.*2825G>A, NR_073534.2:n.3499G>A, NR_073534.1:n.3513G>A, XM_017022581.2:c.*2825G>A, XM_017022581.1:c.*2825G>A

Select item 148893869018.

rs1488938690 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:64150647 (GRCh38)
15:64442846 (GRCh37)
Canonical SPDI:: NC_000015.10:64150646:A:G
Gene:: SNX22 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_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_000015.10:g.64150647A>G, NC_000015.9:g.64442846A>G, NG_033071.1:g.3931A>G

Select item 148867165419.

rs1488671654 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:64157248 (GRCh38)
15:64449447 (GRCh37)
Canonical SPDI:: NC_000015.10:64157247:T:G
Gene:: PPIB (Varview), SNX22 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.64157248T>G, NC_000015.9:g.64449447T>G, NG_012979.1:g.10908A>C, NG_033071.1:g.10532T>G, NM_024798.3:c.*2740T>G, NM_024798.2:c.*2740T>G, NR_073534.2:n.3414T>G, NR_073534.1:n.3428T>G, XM_017022581.2:c.*2740T>G, XM_017022581.1:c.*2740T>G

Select item 148838720820.

rs1488387208 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:64149612 (GRCh38)
15:64441811 (GRCh37)
Canonical SPDI:: NC_000015.10:64149611:C:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.64149612C>G, NC_000015.9:g.64441811C>G, NG_033071.1:g.2896C>G

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