SNP Links for Gene (Select 731424) - SNP

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Select item 14915829311.

rs1491582931 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 4:184856096 (GRCh38)
4:185777250 (GRCh37)
Canonical SPDI:: NC_000004.12:184856095:CA:
Gene:: MIR3945HG (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.02554/303 (ALFA)
-=0.00326/92 (TOMMO)
HGVS:: NC_000004.12:g.184856096_184856097del, NC_000004.11:g.185777250_185777251del

Select item 14915797612.

rs1491579761 has merged into rs11322811 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:184844572 (GRCh38)
4:185765726 (GRCh37)
Canonical SPDI:: NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: MIR3945HG (Varview), LOC105377587 (Varview)
Functional Consequence:: downstream_transcript_variant,non_coding_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000004.12:g.184844572_184844580del, NC_000004.12:g.184844573_184844580del, NC_000004.12:g.184844574_184844580del, NC_000004.12:g.184844575_184844580del, NC_000004.12:g.184844576_184844580del, NC_000004.12:g.184844577_184844580del, NC_000004.12:g.184844578_184844580del, NC_000004.12:g.184844579_184844580del, NC_000004.12:g.184844580del, NC_000004.12:g.184844580dup, NC_000004.12:g.184844579_184844580dup, NC_000004.12:g.184844578_184844580dup, NC_000004.12:g.184844577_184844580dup, NC_000004.12:g.184844576_184844580dup, NC_000004.12:g.184844575_184844580dup, NC_000004.12:g.184844574_184844580dup, NC_000004.12:g.184844573_184844580dup, NC_000004.12:g.184844569_184844580dup, NC_000004.12:g.184844568_184844580dup, NC_000004.12:g.184844565_184844580dup, NC_000004.11:g.185765726_185765734del, NC_000004.11:g.185765727_185765734del, NC_000004.11:g.185765728_185765734del, NC_000004.11:g.185765729_185765734del, NC_000004.11:g.185765730_185765734del, NC_000004.11:g.185765731_185765734del, NC_000004.11:g.185765732_185765734del, NC_000004.11:g.185765733_185765734del, NC_000004.11:g.185765734del, NC_000004.11:g.185765734dup, NC_000004.11:g.185765733_185765734dup, NC_000004.11:g.185765732_185765734dup, NC_000004.11:g.185765731_185765734dup, NC_000004.11:g.185765730_185765734dup, NC_000004.11:g.185765729_185765734dup, NC_000004.11:g.185765728_185765734dup, NC_000004.11:g.185765727_185765734dup, NC_000004.11:g.185765723_185765734dup, NC_000004.11:g.185765722_185765734dup, NC_000004.11:g.185765719_185765734dup, NR_037867.1:n.2116_2124del, NR_037867.1:n.2117_2124del, NR_037867.1:n.2118_2124del, NR_037867.1:n.2119_2124del, NR_037867.1:n.2120_2124del, NR_037867.1:n.2121_2124del, NR_037867.1:n.2122_2124del, NR_037867.1:n.2123_2124del, NR_037867.1:n.2124del, NR_037867.1:n.2124dup, NR_037867.1:n.2123_2124dup, NR_037867.1:n.2122_2124dup, NR_037867.1:n.2121_2124dup, NR_037867.1:n.2120_2124dup, NR_037867.1:n.2119_2124dup, NR_037867.1:n.2118_2124dup, NR_037867.1:n.2117_2124dup, NR_037867.1:n.2113_2124dup, NR_037867.1:n.2112_2124dup, NR_037867.1:n.2109_2124dup, NR_132989.1:n.645_653del, NR_132989.1:n.646_653del, NR_132989.1:n.647_653del, NR_132989.1:n.648_653del, NR_132989.1:n.649_653del, NR_132989.1:n.650_653del, NR_132989.1:n.651_653del, NR_132989.1:n.652_653del, NR_132989.1:n.653del, NR_132989.1:n.653dup, NR_132989.1:n.652_653dup, NR_132989.1:n.651_653dup, NR_132989.1:n.650_653dup, NR_132989.1:n.649_653dup, NR_132989.1:n.648_653dup, NR_132989.1:n.647_653dup, NR_132989.1:n.646_653dup, NR_132989.1:n.642_653dup, NR_132989.1:n.641_653dup, NR_132989.1:n.638_653dup

Select item 14912682153.

rs1491268215 [Homo sapiens]

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

Select item 14911756564.

rs1491175656 has merged into rs35041415 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 4:184856108 (GRCh38)
4:185777262 (GRCh37)
Canonical SPDI:: NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:184856096:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MIR3945HG (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000004.12:g.184856108_184856120del, NC_000004.12:g.184856109_184856120del, NC_000004.12:g.184856110_184856120del, NC_000004.12:g.184856111_184856120del, NC_000004.12:g.184856113_184856120del, NC_000004.12:g.184856114_184856120del, NC_000004.12:g.184856115_184856120del, NC_000004.12:g.184856116_184856120del, NC_000004.12:g.184856117_184856120del, NC_000004.12:g.184856118_184856120del, NC_000004.12:g.184856119_184856120del, NC_000004.12:g.184856120del, NC_000004.12:g.184856120dup, NC_000004.12:g.184856119_184856120dup, NC_000004.12:g.184856118_184856120dup, NC_000004.12:g.184856117_184856120dup, NC_000004.12:g.184856116_184856120dup, NC_000004.11:g.185777262_185777274del, NC_000004.11:g.185777263_185777274del, NC_000004.11:g.185777264_185777274del, NC_000004.11:g.185777265_185777274del, NC_000004.11:g.185777267_185777274del, NC_000004.11:g.185777268_185777274del, NC_000004.11:g.185777269_185777274del, NC_000004.11:g.185777270_185777274del, NC_000004.11:g.185777271_185777274del, NC_000004.11:g.185777272_185777274del, NC_000004.11:g.185777273_185777274del, NC_000004.11:g.185777274del, NC_000004.11:g.185777274dup, NC_000004.11:g.185777273_185777274dup, NC_000004.11:g.185777272_185777274dup, NC_000004.11:g.185777271_185777274dup, NC_000004.11:g.185777270_185777274dup

Select item 14909910125.

rs1490991012 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:184854258 (GRCh38)
4:185775412 (GRCh37)
Canonical SPDI:: NC_000004.12:184854257:A:G
Gene:: MIR3945HG (Varview)
Functional Consequence:: intron_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_000004.12:g.184854258A>G, NC_000004.11:g.185775412A>G

Select item 14909775626.

rs1490977562 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:184854024 (GRCh38)
4:185775178 (GRCh37)
Canonical SPDI:: NC_000004.12:184854023:G:A
Gene:: MIR3945HG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.184854024G>A, NC_000004.11:g.185775178G>A

Select item 14902993297.

rs1490299329 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 4:184847839 (GRCh38)
4:185768993 (GRCh37)
Canonical SPDI:: NC_000004.12:184847838:G:A,NC_000004.12:184847838:G:T
Gene:: MIR3945HG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.184847839G>A, NC_000004.12:g.184847839G>T, NC_000004.11:g.185768993G>A, NC_000004.11:g.185768993G>T

Select item 14899199328.

rs1489919932 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 4:184848410 (GRCh38)
4:185769564 (GRCh37)
Canonical SPDI:: NC_000004.12:184848409:A:
Gene:: MIR3945HG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.184848410del, NC_000004.11:g.185769564del

Select item 14898165569.

rs1489816556 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 4:184856727 (GRCh38)
4:185777881 (GRCh37)
Canonical SPDI:: NC_000004.12:184856726:G:A,NC_000004.12:184856726:G:T
Gene:: MIR3945HG (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000004.12:g.184856727G>A, NC_000004.12:g.184856727G>T, NC_000004.11:g.185777881G>A, NC_000004.11:g.185777881G>T

Select item 148942762710.

rs1489427627 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 4:184845474 (GRCh38)
4:185766628 (GRCh37)
Canonical SPDI:: NC_000004.12:184845473:T:G
Gene:: MIR3945HG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.184845474T>G, NC_000004.11:g.185766628T>G, NR_037867.1:n.1212A>C

Select item 148937960211.

rs1489379602 has merged into rs11322811 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:184844572 (GRCh38)
4:185765726 (GRCh37)
Canonical SPDI:: NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:184844561:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: MIR3945HG (Varview), LOC105377587 (Varview)
Functional Consequence:: downstream_transcript_variant,non_coding_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000004.12:g.184844572_184844580del, NC_000004.12:g.184844573_184844580del, NC_000004.12:g.184844574_184844580del, NC_000004.12:g.184844575_184844580del, NC_000004.12:g.184844576_184844580del, NC_000004.12:g.184844577_184844580del, NC_000004.12:g.184844578_184844580del, NC_000004.12:g.184844579_184844580del, NC_000004.12:g.184844580del, NC_000004.12:g.184844580dup, NC_000004.12:g.184844579_184844580dup, NC_000004.12:g.184844578_184844580dup, NC_000004.12:g.184844577_184844580dup, NC_000004.12:g.184844576_184844580dup, NC_000004.12:g.184844575_184844580dup, NC_000004.12:g.184844574_184844580dup, NC_000004.12:g.184844573_184844580dup, NC_000004.12:g.184844569_184844580dup, NC_000004.12:g.184844568_184844580dup, NC_000004.12:g.184844565_184844580dup, NC_000004.11:g.185765726_185765734del, NC_000004.11:g.185765727_185765734del, NC_000004.11:g.185765728_185765734del, NC_000004.11:g.185765729_185765734del, NC_000004.11:g.185765730_185765734del, NC_000004.11:g.185765731_185765734del, NC_000004.11:g.185765732_185765734del, NC_000004.11:g.185765733_185765734del, NC_000004.11:g.185765734del, NC_000004.11:g.185765734dup, NC_000004.11:g.185765733_185765734dup, NC_000004.11:g.185765732_185765734dup, NC_000004.11:g.185765731_185765734dup, NC_000004.11:g.185765730_185765734dup, NC_000004.11:g.185765729_185765734dup, NC_000004.11:g.185765728_185765734dup, NC_000004.11:g.185765727_185765734dup, NC_000004.11:g.185765723_185765734dup, NC_000004.11:g.185765722_185765734dup, NC_000004.11:g.185765719_185765734dup, NR_037867.1:n.2116_2124del, NR_037867.1:n.2117_2124del, NR_037867.1:n.2118_2124del, NR_037867.1:n.2119_2124del, NR_037867.1:n.2120_2124del, NR_037867.1:n.2121_2124del, NR_037867.1:n.2122_2124del, NR_037867.1:n.2123_2124del, NR_037867.1:n.2124del, NR_037867.1:n.2124dup, NR_037867.1:n.2123_2124dup, NR_037867.1:n.2122_2124dup, NR_037867.1:n.2121_2124dup, NR_037867.1:n.2120_2124dup, NR_037867.1:n.2119_2124dup, NR_037867.1:n.2118_2124dup, NR_037867.1:n.2117_2124dup, NR_037867.1:n.2113_2124dup, NR_037867.1:n.2112_2124dup, NR_037867.1:n.2109_2124dup, NR_132989.1:n.645_653del, NR_132989.1:n.646_653del, NR_132989.1:n.647_653del, NR_132989.1:n.648_653del, NR_132989.1:n.649_653del, NR_132989.1:n.650_653del, NR_132989.1:n.651_653del, NR_132989.1:n.652_653del, NR_132989.1:n.653del, NR_132989.1:n.653dup, NR_132989.1:n.652_653dup, NR_132989.1:n.651_653dup, NR_132989.1:n.650_653dup, NR_132989.1:n.649_653dup, NR_132989.1:n.648_653dup, NR_132989.1:n.647_653dup, NR_132989.1:n.646_653dup, NR_132989.1:n.642_653dup, NR_132989.1:n.641_653dup, NR_132989.1:n.638_653dup

Select item 148935683612.

rs1489356836 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:184849303 (GRCh38)
4:185770457 (GRCh37)
Canonical SPDI:: NC_000004.12:184849302:G:A
Gene:: MIR3945HG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.184849303G>A, NC_000004.11:g.185770457G>A

Select item 148913531213.

rs1489135312 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:184856423 (GRCh38)
4:185777577 (GRCh37)
Canonical SPDI:: NC_000004.12:184856422:A:G
Gene:: MIR3945HG (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.184856423A>G, NC_000004.11:g.185777577A>G

Select item 148884549814.

rs1488845498 [Homo sapiens]

Variant type:: DEL
Alleles:: CAAAA>- [Show Flanks]
Chromosome:: 4:184856096 (GRCh38)
4:185777250 (GRCh37)
Canonical SPDI:: NC_000004.12:184856095:CAAAA:
Gene:: MIR3945HG (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
-=0.00003/1 (GnomAD)
HGVS:: NC_000004.12:g.184856096_184856100del, NC_000004.11:g.185777250_185777254del

Select item 148825935815.

rs1488259358 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:184856023 (GRCh38)
4:185777177 (GRCh37)
Canonical SPDI:: NC_000004.12:184856022:G:A
Gene:: MIR3945HG (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.184856023G>A, NC_000004.11:g.185777177G>A

Select item 148815719516.

rs1488157195 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:184856840 (GRCh38)
4:185777994 (GRCh37)
Canonical SPDI:: NC_000004.12:184856839:A:C
Gene:: MIR3945HG (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000004.12:g.184856840A>C, NC_000004.11:g.185777994A>C

Select item 148784694717.

rs1487846947 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:184853899 (GRCh38)
4:185775053 (GRCh37)
Canonical SPDI:: NC_000004.12:184853898:T:C
Gene:: MIR3945HG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: C=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.184853899T>C, NC_000004.11:g.185775053T>C

Select item 148779451418.

rs1487794514 [Homo sapiens]

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

Select item 148757558919.

rs1487575589 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:184849424 (GRCh38)
4:185770578 (GRCh37)
Canonical SPDI:: NC_000004.12:184849423:C:A
Gene:: MIR3945HG (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000004.12:g.184849424C>A, NC_000004.11:g.185770578C>A

Select item 148742310020.

rs1487423100 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:184842934 (GRCh38)
4:185764088 (GRCh37)
Canonical SPDI:: NC_000004.12:184842933:T:C
Gene:: MIR3945HG (Varview), LOC105377587 (Varview)
Functional Consequence:: intron_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.184842934T>C, NC_000004.11:g.185764088T>C

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