SNP Links for Gene (Select 54931) - SNP

Links from Gene

Items: 1 to 20 of 1804

<< First< Prev

Page of 91

Next >Last >>

Select item 14912645531.

rs1491264553 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTTT [Show Flanks]
Chromosome:: 3:101561335 (GRCh38)
3:101280180 (GRCh37)
Canonical SPDI:: NC_000003.12:101561335:TTT:TTTGTTT
Gene:: TRMT10C (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTGTTT=0./0 (ALFA)
TTTG=0.00116/16 (TOMMO)
TTTG=0.00117/15 (GnomAD)
TTTG=0.00513/9 (Korea1K)
HGVS:: NC_000003.12:g.101561338_101561339insGTTT, NC_000003.11:g.101280182_101280183insGTTT, NG_050898.1:g.4503_4504insGTTT

Select item 14911886642.

rs1491188664 has merged into rs761607951 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:101561346 (GRCh38)
3:101280190 (GRCh37)
Canonical SPDI:: NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:101561334:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: TRMT10C (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000003.12:g.101561346_101561361del, NC_000003.12:g.101561347_101561361del, NC_000003.12:g.101561348_101561361del, NC_000003.12:g.101561349_101561361del, NC_000003.12:g.101561350_101561361del, NC_000003.12:g.101561351_101561361del, NC_000003.12:g.101561352_101561361del, NC_000003.12:g.101561353_101561361del, NC_000003.12:g.101561354_101561361del, NC_000003.12:g.101561355_101561361del, NC_000003.12:g.101561356_101561361del, NC_000003.12:g.101561357_101561361del, NC_000003.12:g.101561358_101561361del, NC_000003.12:g.101561359_101561361del, NC_000003.12:g.101561360_101561361del, NC_000003.12:g.101561361del, NC_000003.12:g.101561361dup, NC_000003.12:g.101561360_101561361dup, NC_000003.12:g.101561359_101561361dup, NC_000003.12:g.101561358_101561361dup, NC_000003.12:g.101561357_101561361dup, NC_000003.12:g.101561356_101561361dup, NC_000003.12:g.101561355_101561361dup, NC_000003.12:g.101561354_101561361dup, NC_000003.12:g.101561353_101561361dup, NC_000003.12:g.101561352_101561361dup, NC_000003.12:g.101561351_101561361dup, NC_000003.12:g.101561350_101561361dup, NC_000003.12:g.101561349_101561361dup, NC_000003.12:g.101561348_101561361dup, NC_000003.12:g.101561347_101561361dup, NC_000003.12:g.101561346_101561361dup, NC_000003.12:g.101561344_101561361dup, NC_000003.12:g.101561343_101561361dup, NC_000003.12:g.101561342_101561361dup, NC_000003.12:g.101561341_101561361dup, NC_000003.12:g.101561340_101561361dup, NC_000003.12:g.101561339_101561361dup, NC_000003.12:g.101561338_101561361dup, NC_000003.12:g.101561337_101561361dup, NC_000003.12:g.101561335_101561361dup, NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.101561361_101561362insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.101280190_101280205del, NC_000003.11:g.101280191_101280205del, NC_000003.11:g.101280192_101280205del, NC_000003.11:g.101280193_101280205del, NC_000003.11:g.101280194_101280205del, NC_000003.11:g.101280195_101280205del, NC_000003.11:g.101280196_101280205del, NC_000003.11:g.101280197_101280205del, NC_000003.11:g.101280198_101280205del, NC_000003.11:g.101280199_101280205del, NC_000003.11:g.101280200_101280205del, NC_000003.11:g.101280201_101280205del, NC_000003.11:g.101280202_101280205del, NC_000003.11:g.101280203_101280205del, NC_000003.11:g.101280204_101280205del, NC_000003.11:g.101280205del, NC_000003.11:g.101280205dup, NC_000003.11:g.101280204_101280205dup, NC_000003.11:g.101280203_101280205dup, NC_000003.11:g.101280202_101280205dup, NC_000003.11:g.101280201_101280205dup, NC_000003.11:g.101280200_101280205dup, NC_000003.11:g.101280199_101280205dup, NC_000003.11:g.101280198_101280205dup, NC_000003.11:g.101280197_101280205dup, NC_000003.11:g.101280196_101280205dup, NC_000003.11:g.101280195_101280205dup, NC_000003.11:g.101280194_101280205dup, NC_000003.11:g.101280193_101280205dup, NC_000003.11:g.101280192_101280205dup, NC_000003.11:g.101280191_101280205dup, NC_000003.11:g.101280190_101280205dup, NC_000003.11:g.101280188_101280205dup, NC_000003.11:g.101280187_101280205dup, NC_000003.11:g.101280186_101280205dup, NC_000003.11:g.101280185_101280205dup, NC_000003.11:g.101280184_101280205dup, NC_000003.11:g.101280183_101280205dup, NC_000003.11:g.101280182_101280205dup, NC_000003.11:g.101280181_101280205dup, NC_000003.11:g.101280179_101280205dup, NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.101280205_101280206insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_050898.1:g.4511_4526del, NG_050898.1:g.4512_4526del, NG_050898.1:g.4513_4526del, NG_050898.1:g.4514_4526del, NG_050898.1:g.4515_4526del, NG_050898.1:g.4516_4526del, NG_050898.1:g.4517_4526del, NG_050898.1:g.4518_4526del, NG_050898.1:g.4519_4526del, NG_050898.1:g.4520_4526del, NG_050898.1:g.4521_4526del, NG_050898.1:g.4522_4526del, NG_050898.1:g.4523_4526del, NG_050898.1:g.4524_4526del, NG_050898.1:g.4525_4526del, NG_050898.1:g.4526del, NG_050898.1:g.4526dup, NG_050898.1:g.4525_4526dup, NG_050898.1:g.4524_4526dup, NG_050898.1:g.4523_4526dup, NG_050898.1:g.4522_4526dup, NG_050898.1:g.4521_4526dup, NG_050898.1:g.4520_4526dup, NG_050898.1:g.4519_4526dup, NG_050898.1:g.4518_4526dup, NG_050898.1:g.4517_4526dup, NG_050898.1:g.4516_4526dup, NG_050898.1:g.4515_4526dup, NG_050898.1:g.4514_4526dup, NG_050898.1:g.4513_4526dup, NG_050898.1:g.4512_4526dup, NG_050898.1:g.4511_4526dup, NG_050898.1:g.4509_4526dup, NG_050898.1:g.4508_4526dup, NG_050898.1:g.4507_4526dup, NG_050898.1:g.4506_4526dup, NG_050898.1:g.4505_4526dup, NG_050898.1:g.4504_4526dup, NG_050898.1:g.4503_4526dup, NG_050898.1:g.4502_4526dup, NG_050898.1:g.4500_4526dup, NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_050898.1:g.4526_4527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14909810643.

rs1490981064 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:101565159 (GRCh38)
3:101284003 (GRCh37)
Canonical SPDI:: NC_000003.12:101565158:C:A
Gene:: TRMT10C (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000003.12:g.101565159C>A, NC_000003.11:g.101284003C>A, NG_050898.1:g.8324C>A, NM_017819.4:c.378C>A, NM_017819.3:c.378C>A, NP_060289.2:p.Asn126Lys

Select item 14908815944.

rs1490881594 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:101562129 (GRCh38)
3:101280973 (GRCh37)
Canonical SPDI:: NC_000003.12:101562128:T:C
Gene:: TRMT10C (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_000003.12:g.101562129T>C, NC_000003.11:g.101280973T>C, NG_050898.1:g.5294T>C

Select item 14908659005.

rs1490865900 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:101561546 (GRCh38)
3:101280390 (GRCh37)
Canonical SPDI:: NC_000003.12:101561545:A:G
Gene:: TRMT10C (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000034/9 (TOPMED)
HGVS:: NC_000003.12:g.101561546A>G, NC_000003.11:g.101280390A>G, NG_050898.1:g.4711A>G

Select item 14907109416.

rs1490710941 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 3:101566305 (GRCh38)
3:101285149 (GRCh37)
Canonical SPDI:: NC_000003.12:101566304:T:G
Gene:: TRMT10C (Varview)
Functional Consequence:: 3_prime_UTR_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_000003.12:g.101566305T>G, NC_000003.11:g.101285149T>G, NG_050898.1:g.9470T>G, NM_017819.4:c.*312T>G, NM_017819.3:c.*312T>G

Select item 14905778027.

rs1490577802 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:101562330 (GRCh38)
3:101281174 (GRCh37)
Canonical SPDI:: NC_000003.12:101562329:C:T
Gene:: TRMT10C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000003.12:g.101562330C>T, NC_000003.11:g.101281174C>T, NG_050898.1:g.5495C>T

Select item 14904896148.

rs1490489614 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:101565535 (GRCh38)
3:101284379 (GRCh37)
Canonical SPDI:: NC_000003.12:101565534:G:A
Gene:: TRMT10C (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.101565535G>A, NC_000003.11:g.101284379G>A, NG_050898.1:g.8700G>A, NM_017819.4:c.754G>A, NM_017819.3:c.754G>A, NP_060289.2:p.Gly252Ser

Select item 14897282069.

rs1489728206 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:101561658 (GRCh38)
3:101280502 (GRCh37)
Canonical SPDI:: NC_000003.12:101561657:T:C
Gene:: TRMT10C (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0.00008/1 (ALFA)
HGVS:: NC_000003.12:g.101561658T>C, NC_000003.11:g.101280502T>C, NG_050898.1:g.4823T>C

Select item 148966220510.

rs1489662205 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 3:101563046 (GRCh38)
3:101281890 (GRCh37)
Canonical SPDI:: NC_000003.12:101563045:T:G
Gene:: TRMT10C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000003.12:g.101563046T>G, NC_000003.11:g.101281890T>G, NG_050898.1:g.6211T>G

Select item 148801268611.

rs1488012686 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 3:101560883 (GRCh38)
3:101279727 (GRCh37)
Canonical SPDI:: NC_000003.12:101560882:C:G
Gene:: TRMT10C (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.101560883C>G, NC_000003.11:g.101279727C>G, NG_050898.1:g.4048C>G

Select item 148793604812.

rs1487936048 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 3:101566801 (GRCh38)
3:101285645 (GRCh37)
Canonical SPDI:: NC_000003.12:101566800:A:G,NC_000003.12:101566800:A:T
Gene:: TRMT10C (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.101566801A>G, NC_000003.12:g.101566801A>T, NC_000003.11:g.101285645A>G, NC_000003.11:g.101285645A>T, NG_050898.1:g.9966A>G, NG_050898.1:g.9966A>T

Select item 148773580913.

rs1487735809 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:101562592 (GRCh38)
3:101281436 (GRCh37)
Canonical SPDI:: NC_000003.12:101562591:C:T
Gene:: TRMT10C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.000084/1 (ALFA)
T=0.000029/4 (GnomAD)
HGVS:: NC_000003.12:g.101562592C>T, NC_000003.11:g.101281436C>T, NG_050898.1:g.5757C>T

Select item 148770819714.

rs1487708197 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:101561798 (GRCh38)
3:101280642 (GRCh37)
Canonical SPDI:: NC_000003.12:101561797:T:C
Gene:: TRMT10C (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.101561798T>C, NC_000003.11:g.101280642T>C, NG_050898.1:g.4963T>C

Select item 148758432615.

rs1487584326 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 3:101566003 (GRCh38)
3:101284847 (GRCh37)
Canonical SPDI:: NC_000003.12:101566002:A:C,NC_000003.12:101566002:A:G
Gene:: TRMT10C (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by cluster
MAF:: C=0.000005/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.101566003A>C, NC_000003.12:g.101566003A>G, NC_000003.11:g.101284847A>C, NC_000003.11:g.101284847A>G, NG_050898.1:g.9168A>C, NG_050898.1:g.9168A>G, NM_017819.4:c.*10A>C, NM_017819.4:c.*10A>G, NM_017819.3:c.*10A>C, NM_017819.3:c.*10A>G

Select item 148623635816.

rs1486236358 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:101566370 (GRCh38)
3:101285214 (GRCh37)
Canonical SPDI:: NC_000003.12:101566369:A:C
Gene:: TRMT10C (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.101566370A>C, NC_000003.11:g.101285214A>C, NG_050898.1:g.9535A>C, NM_017819.4:c.*377A>C, NM_017819.3:c.*377A>C

Select item 148547284017.

rs1485472840 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:101565313 (GRCh38)
3:101284157 (GRCh37)
Canonical SPDI:: NC_000003.12:101565312:C:A
Gene:: TRMT10C (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.101565313C>A, NC_000003.11:g.101284157C>A, NG_050898.1:g.8478C>A, NM_017819.4:c.532C>A, NM_017819.3:c.532C>A, NP_060289.2:p.Leu178Ile

Select item 148482662118.

rs1484826621 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:101561543 (GRCh38)
3:101280387 (GRCh37)
Canonical SPDI:: NC_000003.12:101561542:A:G
Gene:: TRMT10C (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_000003.12:g.101561543A>G, NC_000003.11:g.101280387A>G, NG_050898.1:g.4708A>G

Select item 148479547219.

rs1484795472 has merged into rs1218064316 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:101562688 (GRCh38)
3:101281532 (GRCh37)
Canonical SPDI:: NC_000003.12:101562684:TTTTTTTTTTTTTT:TTT,NC_000003.12:101562684:TTTTTTTTTTTTTT:TTTT,NC_000003.12:101562684:TTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:101562684:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:101562684:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:101562684:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:101562684:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT
Gene:: TRMT10C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.033725/565 (TOMMO)
-=0.048035/88 (Korea1K)
HGVS:: NC_000003.12:g.101562688_101562698del, NC_000003.12:g.101562689_101562698del, NC_000003.12:g.101562696_101562698del, NC_000003.12:g.101562697_101562698del, NC_000003.12:g.101562698del, NC_000003.12:g.101562698dup, NC_000003.12:g.101562697_101562698dup, NC_000003.11:g.101281532_101281542del, NC_000003.11:g.101281533_101281542del, NC_000003.11:g.101281540_101281542del, NC_000003.11:g.101281541_101281542del, NC_000003.11:g.101281542del, NC_000003.11:g.101281542dup, NC_000003.11:g.101281541_101281542dup, NG_050898.1:g.5853_5863del, NG_050898.1:g.5854_5863del, NG_050898.1:g.5861_5863del, NG_050898.1:g.5862_5863del, NG_050898.1:g.5863del, NG_050898.1:g.5863dup, NG_050898.1:g.5862_5863dup

Select item 148396981720.

rs1483969817 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:101563288 (GRCh38)
3:101282132 (GRCh37)
Canonical SPDI:: NC_000003.12:101563287:C:T
Gene:: TRMT10C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000015/2 (GnomAD)
HGVS:: NC_000003.12:g.101563288C>T, NC_000003.11:g.101282132C>T, NG_050898.1:g.6453C>T

<< First< Prev

Page of 91

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 1804

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity