SNP Links for Nucleotide (Select 491231305) - SNP

Links from Nucleotide

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Select item 14875418701.

rs1487541870 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:82355265 (GRCh38)
15:82647483 (GRCh37)
Canonical SPDI:: NC_000015.10:82355264:C:A
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00004/4 (GnomAD)
A=0.00158/2 (Korea1K)
A=0.00402/48 (TOMMO)
A=0.01581/32 (KOREAN)
HGVS:: NC_000015.10:g.82355265C>A, NC_000015.9:g.82647483C>A, NT_187606.1:g.65325C>A, NR_004847.3:n.130C>A, NR_004847.2:n.198C>A, NR_024474.1:n.198C>A, NR_102747.1:n.221C>A, NR_102748.1:n.221C>A, NR_160936.1:n.208C>A, NR_158179.1:n.194C>A

Select item 14868536612.

rs1486853661 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 15:82355247 (GRCh38)
15:82647465 (GRCh37)
Canonical SPDI:: NC_000015.10:82355246:G:T
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000015.10:g.82355247G>T, NC_000015.9:g.82647465G>T, NT_187606.1:g.65307G>T, NR_004847.3:n.112G>T, NR_004847.2:n.180G>T, NR_024474.1:n.180G>T, NR_102747.1:n.203G>T, NR_102748.1:n.203G>T, NR_160936.1:n.190G>T, NR_158179.1:n.176G>T

Select item 14810993123.

rs1481099312 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:82355085 (GRCh38)
15:82647303 (GRCh37)
Canonical SPDI:: NC_000015.10:82355084:C:T
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000015.10:g.82355085C>T, NC_000015.9:g.82647303C>T, NT_187606.1:g.65145C>T, NR_004847.2:n.18C>T, NR_024474.1:n.18C>T, NR_102747.1:n.41C>T, NR_102748.1:n.41C>T, NR_160936.1:n.28C>T, NR_158179.1:n.14C>T

Select item 14769507744.

rs1476950774 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 15:82355100 (GRCh38)
15:82647318 (GRCh37)
Canonical SPDI:: NC_000015.10:82355099:G:A,NC_000015.10:82355099:G:C
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
A=0.00001/1 (GnomAD)
HGVS:: NC_000015.10:g.82355100G>A, NC_000015.10:g.82355100G>C, NC_000015.9:g.82647318G>A, NC_000015.9:g.82647318G>C, NT_187606.1:g.65160G>A, NT_187606.1:g.65160G>C, NR_004847.2:n.33G>A, NR_004847.2:n.33G>C, NR_024474.1:n.33G>A, NR_024474.1:n.33G>C, NR_102747.1:n.56G>A, NR_102747.1:n.56G>C, NR_102748.1:n.56G>A, NR_102748.1:n.56G>C, NR_160936.1:n.43G>A, NR_160936.1:n.43G>C, NR_158179.1:n.29G>A, NR_158179.1:n.29G>C

Select item 14671965295.

rs1467196529 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:82355123 (GRCh38)
15:82647341 (GRCh37)
Canonical SPDI:: NC_000015.10:82355122:C:G
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.82355123C>G, NC_000015.9:g.82647341C>G, NT_187606.1:g.65183C>G, NR_004847.2:n.56C>G, NR_024474.1:n.56C>G, NR_102747.1:n.79C>G, NR_102748.1:n.79C>G, NR_160936.1:n.66C>G, NR_158179.1:n.52C>G

Select item 14658845156.

rs1465884515 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:82355190 (GRCh38)
15:82647408 (GRCh37)
Canonical SPDI:: NC_000015.10:82355189:G:A
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00093/11 (ALFA)
A=0.00035/9 (TOMMO)
HGVS:: NC_000015.10:g.82355190G>A, NC_000015.9:g.82647408A>G, NT_187606.1:g.65250A>G, NR_004847.3:n.55G>A, NR_004847.2:n.123A>G, NR_024474.1:n.123A>G, NR_102747.1:n.146A>G, NR_102748.1:n.146A>G, NR_160936.1:n.133G>A, NR_158179.1:n.119G>A

Select item 14657939677.

rs1465793967 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 15:82355070 (GRCh38)
15:82647288 (GRCh37)
Canonical SPDI:: NC_000015.10:82355069:G:A,NC_000015.10:82355069:G:C
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000015.10:g.82355070G>A, NC_000015.10:g.82355070G>C, NC_000015.9:g.82647288G>A, NC_000015.9:g.82647288G>C, NT_187606.1:g.65130G>A, NT_187606.1:g.65130G>C, NR_004847.2:n.3G>A, NR_004847.2:n.3G>C, NR_024474.1:n.3G>A, NR_024474.1:n.3G>C, NR_102747.1:n.26G>A, NR_102747.1:n.26G>C, NR_102748.1:n.26G>A, NR_102748.1:n.26G>C, NR_160936.1:n.13G>A, NR_160936.1:n.13G>C

Select item 14596819918.

rs1459681991 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 15:82355142 (GRCh38)
15:82647360 (GRCh37)
Canonical SPDI:: NC_000015.10:82355141:G:A,NC_000015.10:82355141:G:C,NC_000015.10:82355141:G:T
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00001/1 (GnomAD)
C=0.000109/1 (TOMMO)
HGVS:: NC_000015.10:g.82355142G>A, NC_000015.10:g.82355142G>C, NC_000015.10:g.82355142G>T, NC_000015.9:g.82647360G>A, NC_000015.9:g.82647360G>C, NC_000015.9:g.82647360G>T, NT_187606.1:g.65202G>A, NT_187606.1:g.65202G>C, NT_187606.1:g.65202G>T, NR_004847.3:n.7G>A, NR_004847.3:n.7G>C, NR_004847.3:n.7G>T, NR_004847.2:n.75G>A, NR_004847.2:n.75G>C, NR_004847.2:n.75G>T, NR_024474.1:n.75G>A, NR_024474.1:n.75G>C, NR_024474.1:n.75G>T, NR_102747.1:n.98G>A, NR_102747.1:n.98G>C, NR_102747.1:n.98G>T, NR_102748.1:n.98G>A, NR_102748.1:n.98G>C, NR_102748.1:n.98G>T, NR_160936.1:n.85G>A, NR_160936.1:n.85G>C, NR_160936.1:n.85G>T, NR_158179.1:n.71G>A, NR_158179.1:n.71G>C, NR_158179.1:n.71G>T

Select item 14575082539.

rs1457508253 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:82355106 (GRCh38)
15:82647324 (GRCh37)
Canonical SPDI:: NC_000015.10:82355105:T:G
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.82355106T>G, NC_000015.9:g.82647324T>G, NT_187606.1:g.65166T>G, NR_004847.2:n.39T>G, NR_024474.1:n.39T>G, NR_102747.1:n.62T>G, NR_102748.1:n.62T>G, NR_160936.1:n.49T>G, NR_158179.1:n.35T>G

Select item 144644965610.

rs1446449656 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 15:82355120 (GRCh38)
15:82647338 (GRCh37)
Canonical SPDI:: NC_000015.10:82355119:C:G,NC_000015.10:82355119:C:T
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.82355120C>G, NC_000015.10:g.82355120C>T, NC_000015.9:g.82647338C>G, NC_000015.9:g.82647338C>T, NT_187606.1:g.65180C>G, NT_187606.1:g.65180C>T, NR_004847.2:n.53C>G, NR_004847.2:n.53C>T, NR_024474.1:n.53C>G, NR_024474.1:n.53C>T, NR_102747.1:n.76C>G, NR_102747.1:n.76C>T, NR_102748.1:n.76C>G, NR_102748.1:n.76C>T, NR_160936.1:n.63C>G, NR_160936.1:n.63C>T, NR_158179.1:n.49C>G, NR_158179.1:n.49C>T

Select item 143878864011.

rs1438788640 [Homo sapiens]

Variant type:: DELINS
Alleles:: TAGCCGGTGCGCGGGGTGGCTGG>- [Show Flanks]
Chromosome:: 15:82355137 (GRCh38)
15:82647355 (GRCh37)
Canonical SPDI:: NC_000015.10:82355135:GTAGCCGGTGCGCGGGGTGGCTGG:G
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.82355137_82355159del, NC_000015.9:g.82647355_82647377del, NT_187606.1:g.65197_65219del, NR_004847.3:n.2_24del, NR_004847.2:n.70_92del, NR_024474.1:n.70_92del, NR_102747.1:n.93_115del, NR_102748.1:n.93_115del, NR_160936.1:n.80_102del, NR_158179.1:n.66_88del

Select item 142771238312.

rs1427712383 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 15:82355286 (GRCh38)
15:82647505 (GRCh37)
Canonical SPDI:: NC_000015.10:82355286:GGGGG:GGGGGG
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GGGGGG=0./0 (ALFA)
HGVS:: NC_000015.10:g.82355291dup, NC_000015.9:g.82647509dup, NT_187606.1:g.65351dup, NR_004847.3:n.156dup, NR_004847.2:n.224dup, NR_024474.1:n.224dup, NR_102747.1:n.247dup, NR_102748.1:n.247dup, NR_160936.1:n.234dup, NR_158179.1:n.220dup

Select item 142579345113.

rs1425793451 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:82355091 (GRCh38)
15:82647309 (GRCh37)
Canonical SPDI:: NC_000015.10:82355090:G:A
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.00008/1 (ALFA)
HGVS:: NC_000015.10:g.82355091G>A, NC_000015.9:g.82647309G>A, NT_187606.1:g.65151G>A, NR_004847.2:n.24G>A, NR_024474.1:n.24G>A, NR_102747.1:n.47G>A, NR_102748.1:n.47G>A, NR_160936.1:n.34G>A, NR_158179.1:n.20G>A

Select item 142464945014.

rs1424649450 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 15:82355215 (GRCh38)
15:82647433 (GRCh37)
Canonical SPDI:: NC_000015.10:82355214:C:G,NC_000015.10:82355214:C:T
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00014/2 (ALFA)
HGVS:: NC_000015.10:g.82355215C>G, NC_000015.10:g.82355215C>T, NC_000015.9:g.82647433C>G, NC_000015.9:g.82647433C>T, NT_187606.1:g.65275C>G, NT_187606.1:g.65275C>T, NR_004847.3:n.80C>G, NR_004847.3:n.80C>T, NR_004847.2:n.148C>G, NR_004847.2:n.148C>T, NR_024474.1:n.148C>G, NR_024474.1:n.148C>T, NR_102747.1:n.171C>G, NR_102747.1:n.171C>T, NR_102748.1:n.171C>G, NR_102748.1:n.171C>T, NR_160936.1:n.158C>G, NR_160936.1:n.158C>T, NR_158179.1:n.144C>G, NR_158179.1:n.144C>T

Select item 142440226815.

rs1424402268 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 15:82355322 (GRCh38)
15:82647540 (GRCh37)
Canonical SPDI:: NC_000015.10:82355321:A:G,NC_000015.10:82355321:A:T
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.00002/1 (GnomAD)
HGVS:: NC_000015.10:g.82355322A>G, NC_000015.10:g.82355322A>T, NC_000015.9:g.82647540A>G, NC_000015.9:g.82647540A>T, NT_187606.1:g.65382A>G, NT_187606.1:g.65382A>T, NR_004847.3:n.187A>G, NR_004847.3:n.187A>T, NR_004847.2:n.255A>G, NR_004847.2:n.255A>T, NR_024474.1:n.255A>G, NR_024474.1:n.255A>T, NR_102747.1:n.278A>G, NR_102747.1:n.278A>T, NR_102748.1:n.278A>G, NR_102748.1:n.278A>T, NR_160936.1:n.265A>G, NR_160936.1:n.265A>T, NR_158179.1:n.251A>G, NR_158179.1:n.251A>T

Select item 142024933316.

rs1420249333 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>-
Chromosome:: no mapping
Canonical SPDI:

Select item 141893977717.

rs1418939777 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:82355204 (GRCh38)
15:82647422 (GRCh37)
Canonical SPDI:: NC_000015.10:82355203:G:A
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000019/2 (GnomAD)
HGVS:: NC_000015.10:g.82355204G>A, NC_000015.9:g.82647422G>A, NT_187606.1:g.65264G>A, NR_004847.3:n.69G>A, NR_004847.2:n.137G>A, NR_024474.1:n.137G>A, NR_102747.1:n.160G>A, NR_102748.1:n.160G>A, NR_160936.1:n.147G>A, NR_158179.1:n.133G>A

Select item 141546455418.

rs1415464554 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>G
Chromosome:: no mapping
Canonical SPDI:

Select item 141328227119.

rs1413282271 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:82355239 (GRCh38)
15:82647457 (GRCh37)
Canonical SPDI:: NC_000015.10:82355238:C:G
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.000142/2 (ALFA)
G=0.000019/2 (GnomAD)
HGVS:: NC_000015.10:g.82355239C>G, NC_000015.9:g.82647457C>G, NT_187606.1:g.65299C>G, NR_004847.3:n.104C>G, NR_004847.2:n.172C>G, NR_024474.1:n.172C>G, NR_102747.1:n.195C>G, NR_102748.1:n.195C>G, NR_160936.1:n.182C>G, NR_158179.1:n.168C>G

Select item 141265317620.

rs1412653176 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 15:82355127 (GRCh38)
15:82647345 (GRCh37)
Canonical SPDI:: NC_000015.10:82355126:G:A,NC_000015.10:82355126:G:C
Gene:: UBE2Q2P2 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.82355127G>A, NC_000015.10:g.82355127G>C, NC_000015.9:g.82647345G>A, NC_000015.9:g.82647345G>C, NT_187606.1:g.65187G>A, NT_187606.1:g.65187G>C, NR_004847.2:n.60G>A, NR_004847.2:n.60G>C, NR_024474.1:n.60G>A, NR_024474.1:n.60G>C, NR_102747.1:n.83G>A, NR_102747.1:n.83G>C, NR_102748.1:n.83G>A, NR_102748.1:n.83G>C, NR_160936.1:n.70G>A, NR_160936.1:n.70G>C, NR_158179.1:n.56G>A, NR_158179.1:n.56G>C

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