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Select item 14915864441.

rs1491586444 [Homo sapiens]

Variant type:: DELINS
Alleles:: TC>- [Show Flanks]
Chromosome:: 1:239426147 (GRCh38)
1:239589447 (GRCh37)
Canonical SPDI:: NC_000001.11:239426145:CTC:C
Gene:: CHRM3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
-=0.00005/0 (TOMMO)
HGVS:: NC_000001.11:g.239426147_239426148del, NC_000001.10:g.239589447_239589448del, NG_032046.2:g.44218_44219del

Select item 14915859712.

rs1491585971 has merged into rs34689648 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTT [Show Flanks]
Chromosome:: 1:239623494 (GRCh38)
1:239786794 (GRCh37)
Canonical SPDI:: NC_000001.11:239623483:TTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:239623483:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:239623483:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:239623483:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:239623483:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:239623483:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT
Gene:: CHRM3 (Varview), LOC105373225 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0.0016/12 (ALFA)
HGVS:: NC_000001.11:g.239623494_239623496del, NC_000001.11:g.239623495_239623496del, NC_000001.11:g.239623496del, NC_000001.11:g.239623496dup, NC_000001.11:g.239623495_239623496dup, NC_000001.11:g.239623494_239623496dup, NC_000001.10:g.239786794_239786796del, NC_000001.10:g.239786795_239786796del, NC_000001.10:g.239786796del, NC_000001.10:g.239786796dup, NC_000001.10:g.239786795_239786796dup, NC_000001.10:g.239786794_239786796dup, NG_032046.2:g.241565_241567del, NG_032046.2:g.241566_241567del, NG_032046.2:g.241567del, NG_032046.2:g.241567dup, NG_032046.2:g.241566_241567dup, NG_032046.2:g.241565_241567dup

Select item 14915826393.

rs1491582639 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 1:239580733 (GRCh38)
1:239744033 (GRCh37)
Canonical SPDI:: NC_000001.11:239580732:AA:
Gene:: CHRM3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000035/1 (TOMMO)
-=0.000929/112 (GnomAD)
HGVS:: NC_000001.11:g.239580733_239580734del, NC_000001.10:g.239744033_239744034del, NG_032046.2:g.198804_198805del

Select item 14915795734.

rs1491579573 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AT,ATAT,ATATAT,ATATATAT,ATATATATAT,GTATATATAT [Show Flanks]
Chromosome:: 1:239859817 (GRCh38)
1:240023118 (GRCh37)
Canonical SPDI:: NC_000001.11:239859817:T:TAT,NC_000001.11:239859817:T:TATAT,NC_000001.11:239859817:T:TATATAT,NC_000001.11:239859817:T:TATATATAT,NC_000001.11:239859817:T:TATATATATAT,NC_000001.11:239859817:T:TGTATATATAT
Gene:: CHRM3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TATAT=0./0 (ALFA)
HGVS:: NC_000001.11:g.239859818_239859819insAT, NC_000001.11:g.239859818_239859819insATAT, NC_000001.11:g.239859819AT[3], NC_000001.11:g.239859819AT[4], NC_000001.11:g.239859819AT[5], NC_000001.11:g.239859818_239859819insGTATATATAT, NC_000001.10:g.240023118_240023119insAT, NC_000001.10:g.240023118_240023119insATAT, NC_000001.10:g.240023119AT[3], NC_000001.10:g.240023119AT[4], NC_000001.10:g.240023119AT[5], NC_000001.10:g.240023118_240023119insGTATATATAT, NG_032046.2:g.477889_477890insAT, NG_032046.2:g.477889_477890insATAT, NG_032046.2:g.477890AT[3], NG_032046.2:g.477890AT[4], NG_032046.2:g.477890AT[5], NG_032046.2:g.477889_477890insGTATATATAT

Select item 14915757575.

rs1491575757 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 1:239662105 (GRCh38)
1:239825406 (GRCh37)
Canonical SPDI:: NC_000001.11:239662105:T:TT
Gene:: CHRM3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.000022/3 (GnomAD)
T=0.000042/11 (TOPMED)
HGVS:: NC_000001.11:g.239662106dup, NC_000001.10:g.239825406dup, NG_032046.2:g.280177dup

Select item 14915693076.

rs1491569307 has merged into rs34901177 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTCTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:239843457 (GRCh38)
1:240006757 (GRCh37)
Canonical SPDI:: NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239843447:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CHRM3 (Varview), LOC124904567 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.4/16 (GENOME_DK)
-=0.4988/2498 (1000Genomes)
HGVS:: NC_000001.11:g.239843457_239843470del, NC_000001.11:g.239843458_239843470del, NC_000001.11:g.239843459_239843470del, NC_000001.11:g.239843460_239843470del, NC_000001.11:g.239843461_239843470del, NC_000001.11:g.239843462_239843470del, NC_000001.11:g.239843463_239843470del, NC_000001.11:g.239843464_239843470del, NC_000001.11:g.239843465_239843470del, NC_000001.11:g.239843466_239843470del, NC_000001.11:g.239843467_239843470del, NC_000001.11:g.239843468_239843470del, NC_000001.11:g.239843469_239843470del, NC_000001.11:g.239843470del, NC_000001.11:g.239843470dup, NC_000001.11:g.239843469_239843470dup, NC_000001.11:g.239843448_239843470T[25]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.11:g.239843468_239843470dup, NC_000001.11:g.239843467_239843470dup, NC_000001.11:g.239843466_239843470dup, NC_000001.11:g.239843465_239843470dup, NC_000001.11:g.239843448_239843470T[29]CTTT[2]T[21], NC_000001.11:g.239843464_239843470dup, NC_000001.11:g.239843448_239843470T[30]CTTTTTTTT[2]T[16], NC_000001.11:g.239843462_239843470dup, NC_000001.11:g.239843448_239843470T[32]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.11:g.239843461_239843470dup, NC_000001.11:g.239843460_239843470dup, NC_000001.11:g.239843459_239843470dup, NC_000001.11:g.239843458_239843470dup, NC_000001.11:g.239843457_239843470dup, NC_000001.11:g.239843456_239843470dup, NC_000001.11:g.239843448_239843470T[39]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.11:g.239843454_239843470dup, NC_000001.11:g.239843448_239843470dup, NC_000001.11:g.239843470_239843471insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.239843470_239843471insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.239843470_239843471insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.239843470_239843471insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.240006757_240006770del, NC_000001.10:g.240006758_240006770del, NC_000001.10:g.240006759_240006770del, NC_000001.10:g.240006760_240006770del, NC_000001.10:g.240006761_240006770del, NC_000001.10:g.240006762_240006770del, NC_000001.10:g.240006763_240006770del, NC_000001.10:g.240006764_240006770del, NC_000001.10:g.240006765_240006770del, NC_000001.10:g.240006766_240006770del, NC_000001.10:g.240006767_240006770del, NC_000001.10:g.240006768_240006770del, NC_000001.10:g.240006769_240006770del, NC_000001.10:g.240006770del, NC_000001.10:g.240006770dup, NC_000001.10:g.240006769_240006770dup, NC_000001.10:g.240006748_240006770T[25]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.10:g.240006768_240006770dup, NC_000001.10:g.240006767_240006770dup, NC_000001.10:g.240006766_240006770dup, NC_000001.10:g.240006765_240006770dup, NC_000001.10:g.240006748_240006770T[29]CTTT[2]T[21], NC_000001.10:g.240006764_240006770dup, NC_000001.10:g.240006748_240006770T[30]CTTTTTTTT[2]T[16], NC_000001.10:g.240006762_240006770dup, NC_000001.10:g.240006748_240006770T[32]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.10:g.240006761_240006770dup, NC_000001.10:g.240006760_240006770dup, NC_000001.10:g.240006759_240006770dup, NC_000001.10:g.240006758_240006770dup, NC_000001.10:g.240006757_240006770dup, NC_000001.10:g.240006756_240006770dup, NC_000001.10:g.240006748_240006770T[39]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000001.10:g.240006754_240006770dup, NC_000001.10:g.240006748_240006770dup, NC_000001.10:g.240006770_240006771insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.240006770_240006771insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.240006770_240006771insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.240006770_240006771insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032046.2:g.461528_461541del, NG_032046.2:g.461529_461541del, NG_032046.2:g.461530_461541del, NG_032046.2:g.461531_461541del, NG_032046.2:g.461532_461541del, NG_032046.2:g.461533_461541del, NG_032046.2:g.461534_461541del, NG_032046.2:g.461535_461541del, NG_032046.2:g.461536_461541del, NG_032046.2:g.461537_461541del, NG_032046.2:g.461538_461541del, NG_032046.2:g.461539_461541del, NG_032046.2:g.461540_461541del, NG_032046.2:g.461541del, NG_032046.2:g.461541dup, NG_032046.2:g.461540_461541dup, NG_032046.2:g.461519_461541T[25]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_032046.2:g.461539_461541dup, NG_032046.2:g.461538_461541dup, NG_032046.2:g.461537_461541dup, NG_032046.2:g.461536_461541dup, NG_032046.2:g.461519_461541T[29]CTTT[2]T[21], NG_032046.2:g.461535_461541dup, NG_032046.2:g.461519_461541T[30]CTTTTTTTT[2]T[16], NG_032046.2:g.461533_461541dup, NG_032046.2:g.461519_461541T[32]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_032046.2:g.461532_461541dup, NG_032046.2:g.461531_461541dup, NG_032046.2:g.461530_461541dup, NG_032046.2:g.461529_461541dup, NG_032046.2:g.461528_461541dup, NG_032046.2:g.461527_461541dup, NG_032046.2:g.461519_461541T[39]CTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_032046.2:g.461525_461541dup, NG_032046.2:g.461519_461541dup, NG_032046.2:g.461541_461542insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032046.2:g.461541_461542insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032046.2:g.461541_461542insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032046.2:g.461541_461542insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14915663727.

rs1491566372 has merged into rs769127124 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:239584118 (GRCh38)
1:239747418 (GRCh37)
Canonical SPDI:: NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:239584108:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CHRM3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000001.11:g.239584118_239584128del, NC_000001.11:g.239584119_239584128del, NC_000001.11:g.239584120_239584128del, NC_000001.11:g.239584121_239584128del, NC_000001.11:g.239584122_239584128del, NC_000001.11:g.239584123_239584128del, NC_000001.11:g.239584124_239584128del, NC_000001.11:g.239584125_239584128del, NC_000001.11:g.239584126_239584128del, NC_000001.11:g.239584127_239584128del, NC_000001.11:g.239584128del, NC_000001.11:g.239584128dup, NC_000001.11:g.239584127_239584128dup, NC_000001.11:g.239584126_239584128dup, NC_000001.11:g.239584125_239584128dup, NC_000001.11:g.239584124_239584128dup, NC_000001.11:g.239584123_239584128dup, NC_000001.11:g.239584122_239584128dup, NC_000001.11:g.239584120_239584128dup, NC_000001.11:g.239584118_239584128dup, NC_000001.11:g.239584117_239584128dup, NC_000001.11:g.239584116_239584128dup, NC_000001.11:g.239584128_239584129insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.239747418_239747428del, NC_000001.10:g.239747419_239747428del, NC_000001.10:g.239747420_239747428del, NC_000001.10:g.239747421_239747428del, NC_000001.10:g.239747422_239747428del, NC_000001.10:g.239747423_239747428del, NC_000001.10:g.239747424_239747428del, NC_000001.10:g.239747425_239747428del, NC_000001.10:g.239747426_239747428del, NC_000001.10:g.239747427_239747428del, NC_000001.10:g.239747428del, NC_000001.10:g.239747428dup, NC_000001.10:g.239747427_239747428dup, NC_000001.10:g.239747426_239747428dup, NC_000001.10:g.239747425_239747428dup, NC_000001.10:g.239747424_239747428dup, NC_000001.10:g.239747423_239747428dup, NC_000001.10:g.239747422_239747428dup, NC_000001.10:g.239747420_239747428dup, NC_000001.10:g.239747418_239747428dup, NC_000001.10:g.239747417_239747428dup, NC_000001.10:g.239747416_239747428dup, NC_000001.10:g.239747428_239747429insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032046.2:g.202189_202199del, NG_032046.2:g.202190_202199del, NG_032046.2:g.202191_202199del, NG_032046.2:g.202192_202199del, NG_032046.2:g.202193_202199del, NG_032046.2:g.202194_202199del, NG_032046.2:g.202195_202199del, NG_032046.2:g.202196_202199del, NG_032046.2:g.202197_202199del, NG_032046.2:g.202198_202199del, NG_032046.2:g.202199del, NG_032046.2:g.202199dup, NG_032046.2:g.202198_202199dup, NG_032046.2:g.202197_202199dup, NG_032046.2:g.202196_202199dup, NG_032046.2:g.202195_202199dup, NG_032046.2:g.202194_202199dup, NG_032046.2:g.202193_202199dup, NG_032046.2:g.202191_202199dup, NG_032046.2:g.202189_202199dup, NG_032046.2:g.202188_202199dup, NG_032046.2:g.202187_202199dup, NG_032046.2:g.202199_202200insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14915514928.

rs1491551492 has merged into rs1175804866 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,AAA,AAAA [Show Flanks]
Chromosome:: 1:239404428 (GRCh38)
1:239567728 (GRCh37)
Canonical SPDI:: NC_000001.11:239404426:AAA:A,NC_000001.11:239404426:AAA:AAAA,NC_000001.11:239404426:AAA:AAAAA
Gene:: CHRM3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.239404428_239404429del, NC_000001.11:g.239404429dup, NC_000001.11:g.239404428_239404429dup, NC_000001.10:g.239567728_239567729del, NC_000001.10:g.239567729dup, NC_000001.10:g.239567728_239567729dup, NG_032046.2:g.22499_22500del, NG_032046.2:g.22500dup, NG_032046.2:g.22499_22500dup

Select item 14915452659.

rs1491545265 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 1:239532010 (GRCh38)
1:239695311 (GRCh37)
Canonical SPDI:: NC_000001.11:239532010::A
Gene:: CHRM3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.00014/3 (GnomAD)
HGVS:: NC_000001.11:g.239532010_239532011insA, NC_000001.10:g.239695310_239695311insA, NG_032046.2:g.150081_150082insA

Select item 149154455310.

rs1491544553 has merged into rs777897145 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,TTATTT [Show Flanks]
Chromosome:: 1:239385819 (GRCh38)
1:239549119 (GRCh37)
Canonical SPDI:: NC_000001.11:239385817:TTT:T,NC_000001.11:239385817:TTT:TTTATTT
Gene:: CHRM3 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.11836/1404 (ALFA)
-=0.00026/12 (GnomAD)
-=0.00541/139 (TOMMO)
HGVS:: NC_000001.11:g.239385819_239385820del, NC_000001.11:g.239385820_239385821insATTT, NC_000001.10:g.239549119_239549120del, NC_000001.10:g.239549120_239549121insATTT, NG_032046.2:g.3890_3891del, NG_032046.2:g.3891_3892insATTT

Select item 149154429111.

rs1491544291 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:239533731 (GRCh38)
1:239697031 (GRCh37)
Canonical SPDI:: NC_000001.11:239533730:CA:
Gene:: CHRM3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00017/2 (ALFA)
HGVS:: NC_000001.11:g.239533731_239533732del, NC_000001.10:g.239697031_239697032del, NG_032046.2:g.151802_151803del

Select item 149154125212.

rs1491541252 has merged into rs57202092 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGTGTGTGTGTGTGTGTGTGTGTGT>-,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
Chromosome:: 1:239662119 (GRCh38)
1:239825419 (GRCh37)
Canonical SPDI:: NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:239662105:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Gene:: CHRM3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGTGTGTGTGT=0./0 (ALFA)
HGVS:: NC_000001.11:g.239662107GT[6], NC_000001.11:g.239662107GT[10], NC_000001.11:g.239662107GT[11], NC_000001.11:g.239662107GT[12], NC_000001.11:g.239662107GT[13], NC_000001.11:g.239662107GT[14], NC_000001.11:g.239662107GT[15], NC_000001.11:g.239662107GT[16], NC_000001.11:g.239662107GT[17], NC_000001.11:g.239662107GT[18], NC_000001.11:g.239662107GT[20], NC_000001.11:g.239662107GT[21], NC_000001.11:g.239662107GT[22], NC_000001.11:g.239662107GT[23], NC_000001.11:g.239662107GT[24], NC_000001.11:g.239662107GT[25], NC_000001.11:g.239662107GT[26], NC_000001.11:g.239662107GT[27], NC_000001.11:g.239662107GT[28], NC_000001.10:g.239825407GT[6], NC_000001.10:g.239825407GT[10], NC_000001.10:g.239825407GT[11], NC_000001.10:g.239825407GT[12], NC_000001.10:g.239825407GT[13], NC_000001.10:g.239825407GT[14], NC_000001.10:g.239825407GT[15], NC_000001.10:g.239825407GT[16], NC_000001.10:g.239825407GT[17], NC_000001.10:g.239825407GT[18], NC_000001.10:g.239825407GT[20], NC_000001.10:g.239825407GT[21], NC_000001.10:g.239825407GT[22], NC_000001.10:g.239825407GT[23], NC_000001.10:g.239825407GT[24], NC_000001.10:g.239825407GT[25], NC_000001.10:g.239825407GT[26], NC_000001.10:g.239825407GT[27], NC_000001.10:g.239825407GT[28], NG_032046.2:g.280178GT[6], NG_032046.2:g.280178GT[10], NG_032046.2:g.280178GT[11], NG_032046.2:g.280178GT[12], NG_032046.2:g.280178GT[13], NG_032046.2:g.280178GT[14], NG_032046.2:g.280178GT[15], NG_032046.2:g.280178GT[16], NG_032046.2:g.280178GT[17], NG_032046.2:g.280178GT[18], NG_032046.2:g.280178GT[20], NG_032046.2:g.280178GT[21], NG_032046.2:g.280178GT[22], NG_032046.2:g.280178GT[23], NG_032046.2:g.280178GT[24], NG_032046.2:g.280178GT[25], NG_032046.2:g.280178GT[26], NG_032046.2:g.280178GT[27], NG_032046.2:g.280178GT[28]

Select item 149154069613.

rs1491540696 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 1:239656469 (GRCh38)
1:239819769 (GRCh37)
Canonical SPDI:: NC_000001.11:239656467:AGA:A
Gene:: CHRM3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000127/17 (GnomAD)
-=0.038296/142 (TWINSUK)
-=0.038402/148 (ALSPAC)
HGVS:: NC_000001.11:g.239656469_239656470del, NC_000001.10:g.239819769_239819770del, NG_032046.2:g.274540_274541del

Select item 149154014814.

rs1491540148 has merged into rs374479816 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACACACACACACACACACACACACACA>-,CA,CACA,CACACA,CACACACA,CACACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA,CACACACACACACACACACACA,CACACACACACACACACACACACA,CACACACACACACACACACACACACA,CACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACA [Show Flanks]
Chromosome:: 1:239580281 (GRCh38)
1:239743581 (GRCh37)
Canonical SPDI:: NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:239580258:CACACACACACACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACACACACACACA
Gene:: CHRM3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACACACACACACA=0./0 (ALFA)
HGVS:: NC_000001.11:g.239580259CA[11], NC_000001.11:g.239580259CA[12], NC_000001.11:g.239580259CA[13], NC_000001.11:g.239580259CA[14], NC_000001.11:g.239580259CA[15], NC_000001.11:g.239580259CA[16], NC_000001.11:g.239580259CA[17], NC_000001.11:g.239580259CA[18], NC_000001.11:g.239580259CA[19], NC_000001.11:g.239580259CA[20], NC_000001.11:g.239580259CA[21], NC_000001.11:g.239580259CA[22], NC_000001.11:g.239580259CA[23], NC_000001.11:g.239580259CA[24], NC_000001.11:g.239580259CA[26], NC_000001.11:g.239580259CA[27], NC_000001.11:g.239580259CA[28], NC_000001.11:g.239580259CA[29], NC_000001.10:g.239743559CA[11], NC_000001.10:g.239743559CA[12], NC_000001.10:g.239743559CA[13], NC_000001.10:g.239743559CA[14], NC_000001.10:g.239743559CA[15], NC_000001.10:g.239743559CA[16], NC_000001.10:g.239743559CA[17], NC_000001.10:g.239743559CA[18], NC_000001.10:g.239743559CA[19], NC_000001.10:g.239743559CA[20], NC_000001.10:g.239743559CA[21], NC_000001.10:g.239743559CA[22], NC_000001.10:g.239743559CA[23], NC_000001.10:g.239743559CA[24], NC_000001.10:g.239743559CA[26], NC_000001.10:g.239743559CA[27], NC_000001.10:g.239743559CA[28], NC_000001.10:g.239743559CA[29], NG_032046.2:g.198330CA[11], NG_032046.2:g.198330CA[12], NG_032046.2:g.198330CA[13], NG_032046.2:g.198330CA[14], NG_032046.2:g.198330CA[15], NG_032046.2:g.198330CA[16], NG_032046.2:g.198330CA[17], NG_032046.2:g.198330CA[18], NG_032046.2:g.198330CA[19], NG_032046.2:g.198330CA[20], NG_032046.2:g.198330CA[21], NG_032046.2:g.198330CA[22], NG_032046.2:g.198330CA[23], NG_032046.2:g.198330CA[24], NG_032046.2:g.198330CA[26], NG_032046.2:g.198330CA[27], NG_032046.2:g.198330CA[28], NG_032046.2:g.198330CA[29]

Select item 149153862615.

rs1491538626 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 1:239576623 (GRCh38)
1:239739924 (GRCh37)
Canonical SPDI:: NC_000001.11:239576623:C:CC
Gene:: CHRM3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: C=0.000177/3 (TOMMO)
C=0.000482/57 (GnomAD)
HGVS:: NC_000001.11:g.239576624dup, NC_000001.10:g.239739924dup, NG_032046.2:g.194695dup

Select item 149152881216.

rs1491528812 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GA [Show Flanks]
Chromosome:: 1:239404361 (GRCh38)
1:239567662 (GRCh37)
Canonical SPDI:: NC_000001.11:239404361:A:AGA
Gene:: CHRM3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: AGA=0./0 (ALFA)
HGVS:: NC_000001.11:g.239404362_239404363insGA, NC_000001.10:g.239567662_239567663insGA, NG_032046.2:g.22433_22434insGA

Select item 149152123417.

rs1491521234 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:239610190 (GRCh38)
1:239773490 (GRCh37)
Canonical SPDI:: NC_000001.11:239610189:CA:
Gene:: CHRM3 (Varview), LOC105373225 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00295/35 (ALFA)
-=0.00075/19 (TOMMO)
HGVS:: NC_000001.11:g.239610190_239610191del, NC_000001.10:g.239773490_239773491del, NG_032046.2:g.228261_228262del

Select item 149151918818.

rs1491519188 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 1:239404437 (GRCh38)
1:239567738 (GRCh37)
Canonical SPDI:: NC_000001.11:239404437:G:GG
Gene:: CHRM3 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
HGVS:: NC_000001.11:g.239404438dup, NC_000001.10:g.239567738dup, NG_032046.2:g.22509dup

Select item 149151713319.

rs1491517133 [Homo sapiens]

Variant type:: INS
Alleles:: ->C,TA,TTA [Show Flanks]
Chromosome:: 1:239623496 (GRCh38)
1:239786797 (GRCh37)
Canonical SPDI:: NC_000001.11:239623496::C,NC_000001.11:239623496::TA,NC_000001.11:239623496::TTA
Gene:: CHRM3 (Varview), LOC105373225 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TA=0./0 (ALFA)
C=0.000128/13 (GnomAD)
HGVS:: NC_000001.11:g.239623496_239623497insC, NC_000001.11:g.239623496_239623497insTA, NC_000001.11:g.239623496_239623497insTTA, NC_000001.10:g.239786796_239786797insC, NC_000001.10:g.239786796_239786797insTA, NC_000001.10:g.239786796_239786797insTTA, NG_032046.2:g.241567_241568insC, NG_032046.2:g.241567_241568insTA, NG_032046.2:g.241567_241568insTTA

Select item 149150396620.

rs1491503966 has merged into rs61441846 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:239533747 (GRCh38)
1:239697047 (GRCh37)
Canonical SPDI:: NC_000001.11:239533731:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:239533731:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:239533731:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:239533731:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:239533731:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:239533731:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:239533731:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:239533731:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:239533731:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:239533731:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: CHRM3 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.239533747_239533750del, NC_000001.11:g.239533748_239533750del, NC_000001.11:g.239533749_239533750del, NC_000001.11:g.239533750del, NC_000001.11:g.239533750dup, NC_000001.11:g.239533749_239533750dup, NC_000001.11:g.239533748_239533750dup, NC_000001.11:g.239533745_239533750dup, NC_000001.11:g.239533739_239533750dup, NC_000001.11:g.239533750_239533751insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.239697047_239697050del, NC_000001.10:g.239697048_239697050del, NC_000001.10:g.239697049_239697050del, NC_000001.10:g.239697050del, NC_000001.10:g.239697050dup, NC_000001.10:g.239697049_239697050dup, NC_000001.10:g.239697048_239697050dup, NC_000001.10:g.239697045_239697050dup, NC_000001.10:g.239697039_239697050dup, NC_000001.10:g.239697050_239697051insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_032046.2:g.151818_151821del, NG_032046.2:g.151819_151821del, NG_032046.2:g.151820_151821del, NG_032046.2:g.151821del, NG_032046.2:g.151821dup, NG_032046.2:g.151820_151821dup, NG_032046.2:g.151819_151821dup, NG_032046.2:g.151816_151821dup, NG_032046.2:g.151810_151821dup, NG_032046.2:g.151821_151822insAAAAAAAAAAAAAAAAAAAAAAAAAAA

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