SNP Links for Gene (Select 693215) - SNP

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Links from Gene

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Select item 14910515111.

rs1491051511 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATTA [Show Flanks]
Chromosome:: 15:72587339 (GRCh38)
15:72879681 (GRCh37)
Canonical SPDI:: NC_000015.10:72587339:ATTA:ATTAATTA
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATTAATTA=0./0 (ALFA)
ATTA=0.000007/1 (GnomAD)
ATTA=0.000011/3 (TOPMED)
HGVS:: NC_000015.10:g.72587340_72587343dup, NC_000015.9:g.72879681_72879684dup, NM_005744.5:c.*4048_*4051dup, NM_005744.4:c.*4048_*4051dup

Select item 14903430462.

rs1490343046 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 15:72587101 (GRCh38)
15:72879442 (GRCh37)
Canonical SPDI:: NC_000015.10:72587100:A:T
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 2KB_upstream_variant,3_prime_UTR_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.72587101A>T, NC_000015.9:g.72879442A>T, NM_005744.5:c.*3809A>T, NM_005744.4:c.*3809A>T

Select item 14894059903.

rs1489405990 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 15:72587173 (GRCh38)
15:72879514 (GRCh37)
Canonical SPDI:: NC_000015.10:72587172:T:A
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 2KB_upstream_variant,3_prime_UTR_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.72587173T>A, NC_000015.9:g.72879514T>A, NM_005744.5:c.*3881T>A, NM_005744.4:c.*3881T>A

Select item 14875014594.

rs1487501459 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:72587798 (GRCh38)
15:72880139 (GRCh37)
Canonical SPDI:: NC_000015.10:72587797:T:C
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,downstream_transcript_variant,500B_downstream_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.72587798T>C, NC_000015.9:g.72880139T>C, NM_005744.5:c.*4506T>C, NM_005744.4:c.*4506T>C

Select item 14848272175.

rs1484827217 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 15:72586134 (GRCh38)
15:72878475 (GRCh37)
Canonical SPDI:: NC_000015.10:72586133:G:T
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 2KB_upstream_variant,3_prime_UTR_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000015.10:g.72586134G>T, NC_000015.9:g.72878475G>T, NM_005744.5:c.*2842G>T, NM_005744.4:c.*2842G>T, NM_005744.3:c.*2842G>T

Select item 14833387306.

rs1483338730 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 15:72586787 (GRCh38)
15:72879128 (GRCh37)
Canonical SPDI:: NC_000015.10:72586786:AA:A
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 2KB_upstream_variant,3_prime_UTR_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.72586788del, NC_000015.9:g.72879129del, NM_005744.5:c.*3496del, NM_005744.4:c.*3496del

Select item 14831505247.

rs1483150524 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 15:72585892 (GRCh38)
15:72878233 (GRCh37)
Canonical SPDI:: NC_000015.10:72585891:C:A,NC_000015.10:72585891:C:T
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 2KB_upstream_variant,3_prime_UTR_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (GnomAD)
HGVS:: NC_000015.10:g.72585892C>A, NC_000015.10:g.72585892C>T, NC_000015.9:g.72878233C>A, NC_000015.9:g.72878233C>T, NM_005744.5:c.*2600C>A, NM_005744.5:c.*2600C>T, NM_005744.4:c.*2600C>A, NM_005744.4:c.*2600C>T, NM_005744.3:c.*2600C>A, NM_005744.3:c.*2600C>T

Select item 14808320168.

rs1480832016 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:72586444 (GRCh38)
15:72878785 (GRCh37)
Canonical SPDI:: NC_000015.10:72586443:A:G
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.72586444A>G, NC_000015.9:g.72878785A>G, NM_005744.5:c.*3152A>G, NM_005744.4:c.*3152A>G, NM_005744.3:c.*3152A>G

Select item 14802323889.

rs1480232388 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:72586097 (GRCh38)
15:72878438 (GRCh37)
Canonical SPDI:: NC_000015.10:72586096:A:G
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000142/2 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000015.10:g.72586097A>G, NC_000015.9:g.72878438A>G, NM_005744.5:c.*2805A>G, NM_005744.4:c.*2805A>G, NM_005744.3:c.*2805A>G

Select item 147937684910.

rs1479376849 [Homo sapiens]

Variant type:: DEL
Alleles:: TAAAA>- [Show Flanks]
Chromosome:: 15:72585526 (GRCh38)
15:72877867 (GRCh37)
Canonical SPDI:: NC_000015.10:72585525:TAAAA:
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: -=0.00007/1 (ALFA)
HGVS:: NC_000015.10:g.72585526_72585530del, NC_000015.9:g.72877867_72877871del, NM_005744.5:c.*2234_*2238del, NM_005744.4:c.*2234_*2238del, NM_005744.3:c.*2234_*2238del

Select item 147930395911.

rs1479303959 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATAAA>- [Show Flanks]
Chromosome:: 15:72586537 (GRCh38)
15:72878878 (GRCh37)
Canonical SPDI:: NC_000015.10:72586530:AATAAAATAAA:AATAAA
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AATAAA=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.72586532ATAAA[1], NC_000015.9:g.72878873ATAAA[1], NM_005744.5:c.*3240ATAAA[1], NM_005744.4:c.*3240ATAAA[1], NM_005744.3:c.*3240ATAAA[1]

Select item 147925251412.

rs1479252514 [Homo sapiens]

Variant type:: DELINS
Alleles:: AATAGTGCCTACCA>- [Show Flanks]
Chromosome:: 15:72587793 (GRCh38)
15:72880134 (GRCh37)
Canonical SPDI:: NC_000015.10:72587790:CAAATAGTGCCTACCA:CA
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: CA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.72587793_72587806del, NC_000015.9:g.72880134_72880147del, NM_005744.5:c.*4501_*4514del, NM_005744.4:c.*4501_*4514del

Select item 147806426313.

rs1478064263 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 15:72587288 (GRCh38)
15:72879629 (GRCh37)
Canonical SPDI:: NC_000015.10:72587287:CC:C
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000008/1 (GnomAD)
HGVS:: NC_000015.10:g.72587289del, NC_000015.9:g.72879630del, NM_005744.5:c.*3997del, NM_005744.4:c.*3997del, NR_030359.1:n.73del

Select item 147609062914.

rs1476090629 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:72586267 (GRCh38)
15:72878608 (GRCh37)
Canonical SPDI:: NC_000015.10:72586266:A:G
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000015.10:g.72586267A>G, NC_000015.9:g.72878608A>G, NM_005744.5:c.*2975A>G, NM_005744.4:c.*2975A>G, NM_005744.3:c.*2975A>G

Select item 147445958115.

rs1474459581 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:72586761 (GRCh38)
15:72879102 (GRCh37)
Canonical SPDI:: NC_000015.10:72586760:T:C
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0.000094/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.72586761T>C, NC_000015.9:g.72879102T>C, NM_005744.5:c.*3469T>C, NM_005744.4:c.*3469T>C

Select item 147383772216.

rs1473837722 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:72587209 (GRCh38)
15:72879550 (GRCh37)
Canonical SPDI:: NC_000015.10:72587208:C:T
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
HGVS:: NC_000015.10:g.72587209C>T, NC_000015.9:g.72879550C>T, NM_005744.5:c.*3917C>T, NM_005744.4:c.*3917C>T

Select item 147241236017.

rs1472412360 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTT [Show Flanks]
Chromosome:: 15:72587310 (GRCh38)
15:72879652 (GRCh37)
Canonical SPDI:: NC_000015.10:72587310:T:TGTT
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency
MAF:: TGT=0.0001/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.72587311_72587312insGTT, NC_000015.9:g.72879652_72879653insGTT, NM_005744.5:c.*4019_*4020insGTT, NM_005744.4:c.*4019_*4020insGTT, NR_030359.1:n.95_96insGTT

Select item 147063605018.

rs1470636050 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:72585328 (GRCh38)
15:72877669 (GRCh37)
Canonical SPDI:: NC_000015.10:72585327:C:T
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.72585328C>T, NC_000015.9:g.72877669C>T, NM_005744.5:c.*2036C>T, NM_005744.4:c.*2036C>T, NM_005744.3:c.*2036C>T

Select item 146802315819.

rs1468023158 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 15:72585272 (GRCh38)
15:72877613 (GRCh37)
Canonical SPDI:: NC_000015.10:72585271:C:G,NC_000015.10:72585271:C:T
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.72585272C>G, NC_000015.10:g.72585272C>T, NC_000015.9:g.72877613C>G, NC_000015.9:g.72877613C>T, NM_005744.5:c.*1980C>G, NM_005744.5:c.*1980C>T, NM_005744.4:c.*1980C>G, NM_005744.4:c.*1980C>T, NM_005744.3:c.*1980C>G, NM_005744.3:c.*1980C>T

Select item 146293887120.

rs1462938871 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:72586369 (GRCh38)
15:72878710 (GRCh37)
Canonical SPDI:: NC_000015.10:72586368:T:G
Gene:: ARIH1 (Varview), MIR630 (Varview)
Functional Consequence:: 3_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_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.72586369T>G, NC_000015.9:g.72878710T>G, NM_005744.5:c.*3077T>G, NM_005744.4:c.*3077T>G, NM_005744.3:c.*3077T>G