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Select item 14915461301.

rs1491546130 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTATAT,TTATAT [Show Flanks]
Chromosome:: 6:111534962 (GRCh38)
6:111856166 (GRCh37)
Canonical SPDI:: NC_000006.12:111534962:TATAT:TATATGTATAT,NC_000006.12:111534962:TATAT:TATATTTATAT
Gene:: TRAF3IP2-AS1 (Varview), LOC107986522 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,genic_downstream_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATGTATAT=0./0 (ALFA)
TATATG=0.00002/1 (GnomAD)
HGVS:: NC_000006.12:g.111534963_111534967TA[2]TGTATAT[1], NC_000006.12:g.111534963_111534967TA[2]TTTATAT[1], NC_000006.11:g.111856166_111856170TA[2]TGTATAT[1], NC_000006.11:g.111856166_111856170TA[2]TTTATAT[1]

Select item 14915280792.

rs1491528079 has merged into rs35454154 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA [Show Flanks]
Chromosome:: 6:111556116 (GRCh38)
6:111877319 (GRCh37)
Canonical SPDI:: NC_000006.12:111556102:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:111556102:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:111556102:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:111556102:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:111556102:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:111556102:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:111556102:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:111556102:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA
Gene:: TRAF3IP2 (Varview), TRAF3IP2-AS1 (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
AA=0.279/1397 (1000Genomes)
HGVS:: NC_000006.12:g.111556116_111556121del, NC_000006.12:g.111556117_111556121del, NC_000006.12:g.111556118_111556121del, NC_000006.12:g.111556119_111556121del, NC_000006.12:g.111556120_111556121del, NC_000006.12:g.111556121del, NC_000006.12:g.111556121dup, NC_000006.12:g.111556120_111556121dup, NC_000006.11:g.111877319_111877324del, NC_000006.11:g.111877320_111877324del, NC_000006.11:g.111877321_111877324del, NC_000006.11:g.111877322_111877324del, NC_000006.11:g.111877323_111877324del, NC_000006.11:g.111877324del, NC_000006.11:g.111877324dup, NC_000006.11:g.111877323_111877324dup, NG_032030.2:g.54771_54776del, NG_032030.2:g.54772_54776del, NG_032030.2:g.54773_54776del, NG_032030.2:g.54774_54776del, NG_032030.2:g.54775_54776del, NG_032030.2:g.54776del, NG_032030.2:g.54776dup, NG_032030.2:g.54775_54776dup, NM_147686.4:c.*3297_*3302del, NM_147686.4:c.*3298_*3302del, NM_147686.4:c.*3299_*3302del, NM_147686.4:c.*3300_*3302del, NM_147686.4:c.*3301_*3302del, NM_147686.4:c.*3302del, NM_147686.4:c.*3302dup, NM_147686.4:c.*3301_*3302dup, NM_147686.3:c.*3297_*3302del, NM_147686.3:c.*3298_*3302del, NM_147686.3:c.*3299_*3302del, NM_147686.3:c.*3300_*3302del, NM_147686.3:c.*3301_*3302del, NM_147686.3:c.*3302del, NM_147686.3:c.*3302dup, NM_147686.3:c.*3301_*3302dup, NM_147200.3:c.*3297_*3302del, NM_147200.3:c.*3298_*3302del, NM_147200.3:c.*3299_*3302del, NM_147200.3:c.*3300_*3302del, NM_147200.3:c.*3301_*3302del, NM_147200.3:c.*3302del, NM_147200.3:c.*3302dup, NM_147200.3:c.*3301_*3302dup, NM_001164281.3:c.*3297_*3302del, NM_001164281.3:c.*3298_*3302del, NM_001164281.3:c.*3299_*3302del, NM_001164281.3:c.*3300_*3302del, NM_001164281.3:c.*3301_*3302del, NM_001164281.3:c.*3302del, NM_001164281.3:c.*3302dup, NM_001164281.3:c.*3301_*3302dup, NM_001164281.2:c.*3297_*3302del, NM_001164281.2:c.*3298_*3302del, NM_001164281.2:c.*3299_*3302del, NM_001164281.2:c.*3300_*3302del, NM_001164281.2:c.*3301_*3302del, NM_001164281.2:c.*3302del, NM_001164281.2:c.*3302dup, NM_001164281.2:c.*3301_*3302dup, NM_001164283.3:c.*3297_*3302del, NM_001164283.3:c.*3298_*3302del, NM_001164283.3:c.*3299_*3302del, NM_001164283.3:c.*3300_*3302del, NM_001164283.3:c.*3301_*3302del, NM_001164283.3:c.*3302del, NM_001164283.3:c.*3302dup, NM_001164283.3:c.*3301_*3302dup, NM_001164283.2:c.*3297_*3302del, NM_001164283.2:c.*3298_*3302del, NM_001164283.2:c.*3299_*3302del, NM_001164283.2:c.*3300_*3302del, NM_001164283.2:c.*3301_*3302del, NM_001164283.2:c.*3302del, NM_001164283.2:c.*3302dup, NM_001164283.2:c.*3301_*3302dup, NR_028338.2:n.5613_5618del, NR_028338.2:n.5614_5618del, NR_028338.2:n.5615_5618del, NR_028338.2:n.5616_5618del, NR_028338.2:n.5617_5618del, NR_028338.2:n.5618del, NR_028338.2:n.5618dup, NR_028338.2:n.5617_5618dup

Select item 14915190453.

rs1491519045 [Homo sapiens]

Variant type:: DEL
Alleles:: AC>- [Show Flanks]
Chromosome:: 6:111520958 (GRCh38)
6:111842161 (GRCh37)
Canonical SPDI:: NC_000006.12:111520957:AC:
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000006.12:g.111520958_111520959del, NC_000006.11:g.111842161_111842162del

Select item 14915000684.

rs1491500068 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 6:111490965 (GRCh38)
6:111812168 (GRCh37)
Canonical SPDI:: NC_000006.12:111490964:TA:
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000006.12:g.111490965_111490966del, NC_000006.11:g.111812168_111812169del

Select item 14914937175.

rs1491493717 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 6:111513527 (GRCh38)
6:111834730 (GRCh37)
Canonical SPDI:: NC_000006.12:111513526:TA:
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.111513527_111513528del, NC_000006.11:g.111834730_111834731del

Select item 14914798616.

rs1491479861 has merged into rs59172608 [Homo sapiens]

Variant type:: DELINS
Alleles:: CCC>-,C,CC,CCCC,CCCCC,CCCCCC,CCCCCCC,CCCCCCCC,CCCCCCCCC,CCCCCCCCCC,CCCCCCCCCCC [Show Flanks]
Chromosome:: 6:111520968 (GRCh38)
6:111842171 (GRCh37)
Canonical SPDI:: NC_000006.12:111520958:CCCCCCCCCCCC:CCCCCCCCC,NC_000006.12:111520958:CCCCCCCCCCCC:CCCCCCCCCC,NC_000006.12:111520958:CCCCCCCCCCCC:CCCCCCCCCCC,NC_000006.12:111520958:CCCCCCCCCCCC:CCCCCCCCCCCCC,NC_000006.12:111520958:CCCCCCCCCCCC:CCCCCCCCCCCCCC,NC_000006.12:111520958:CCCCCCCCCCCC:CCCCCCCCCCCCCCC,NC_000006.12:111520958:CCCCCCCCCCCC:CCCCCCCCCCCCCCCC,NC_000006.12:111520958:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCC,NC_000006.12:111520958:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCCC,NC_000006.12:111520958:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCCCC,NC_000006.12:111520958:CCCCCCCCCCCC:CCCCCCCCCCCCCCCCCCCC
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCCCCCCCCCCCCCC=0./0 (ALFA)
C=0.3734/1870 (1000Genomes)
HGVS:: NC_000006.12:g.111520968_111520970del, NC_000006.12:g.111520969_111520970del, NC_000006.12:g.111520970del, NC_000006.12:g.111520970dup, NC_000006.12:g.111520969_111520970dup, NC_000006.12:g.111520968_111520970dup, NC_000006.12:g.111520967_111520970dup, NC_000006.12:g.111520966_111520970dup, NC_000006.12:g.111520965_111520970dup, NC_000006.12:g.111520964_111520970dup, NC_000006.12:g.111520963_111520970dup, NC_000006.11:g.111842171_111842173del, NC_000006.11:g.111842172_111842173del, NC_000006.11:g.111842173del, NC_000006.11:g.111842173dup, NC_000006.11:g.111842172_111842173dup, NC_000006.11:g.111842171_111842173dup, NC_000006.11:g.111842170_111842173dup, NC_000006.11:g.111842169_111842173dup, NC_000006.11:g.111842168_111842173dup, NC_000006.11:g.111842167_111842173dup, NC_000006.11:g.111842166_111842173dup

Select item 14914486777.

rs1491448677 has merged into rs61692718 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>-,TATA,TATATA,TATATATA,TATATATATA,TATATATATATA [Show Flanks]
Chromosome:: 6:111534975 (GRCh38)
6:111856178 (GRCh37)
Canonical SPDI:: NC_000006.12:111534961:ATATATATATATATA:ATATATATATATA,NC_000006.12:111534961:ATATATATATATATA:ATATATATATATATATA,NC_000006.12:111534961:ATATATATATATATA:ATATATATATATATATATA,NC_000006.12:111534961:ATATATATATATATA:ATATATATATATATATATATA,NC_000006.12:111534961:ATATATATATATATA:ATATATATATATATATATATATA,NC_000006.12:111534961:ATATATATATATATA:ATATATATATATATATATATATATA
Gene:: TRAF3IP2-AS1 (Varview), LOC107986522 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATATATATATA=0./0 (ALFA)
ATATAT=0.32788/1642 (1000Genomes)
HGVS:: NC_000006.12:g.111534963TA[6], NC_000006.12:g.111534963TA[8], NC_000006.12:g.111534963TA[9], NC_000006.12:g.111534963TA[10], NC_000006.12:g.111534963TA[11], NC_000006.12:g.111534963TA[12], NC_000006.11:g.111856166TA[6], NC_000006.11:g.111856166TA[8], NC_000006.11:g.111856166TA[9], NC_000006.11:g.111856166TA[10], NC_000006.11:g.111856166TA[11], NC_000006.11:g.111856166TA[12]

Select item 14914433218.

rs1491443321 [Homo sapiens]

Variant type:: DELINS
Alleles:: GC>- [Show Flanks]
Chromosome:: 6:111520971 (GRCh38)
6:111842174 (GRCh37)
Canonical SPDI:: NC_000006.12:111520969:CGC:C
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000006.12:g.111520971_111520972del, NC_000006.11:g.111842174_111842175del

Select item 14914109109.

rs1491410910 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:111556102 (GRCh38)
6:111877305 (GRCh37)
Canonical SPDI:: NC_000006.12:111556101:CA:
Gene:: TRAF3IP2 (Varview), TRAF3IP2-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.02445/290 (ALFA)
-=0.00159/94 (GnomAD)
-=0.0018/51 (TOMMO)
HGVS:: NC_000006.12:g.111556102_111556103del, NC_000006.11:g.111877305_111877306del, NG_032030.2:g.54776_54777del, NM_147686.4:c.*3302_*3303del, NM_147686.3:c.*3302_*3303del, NM_147200.3:c.*3302_*3303del, NM_001164281.3:c.*3302_*3303del, NM_001164281.2:c.*3302_*3303del, NM_001164283.3:c.*3302_*3303del, NM_001164283.2:c.*3302_*3303del, NR_028338.2:n.5618_5619del

Select item 149139549910.

rs1491395499 has merged into rs66656411 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAA>-,A,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:111515271 (GRCh38)
6:111836474 (GRCh37)
Canonical SPDI:: NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111515261:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
A=0.139/696 (1000Genomes)
A=0.4/16 (GENOME_DK)
HGVS:: NC_000006.12:g.111515271_111515282del, NC_000006.12:g.111515272_111515282del, NC_000006.12:g.111515275_111515282del, NC_000006.12:g.111515277_111515282del, NC_000006.12:g.111515278_111515282del, NC_000006.12:g.111515279_111515282del, NC_000006.12:g.111515280_111515282del, NC_000006.12:g.111515281_111515282del, NC_000006.12:g.111515282del, NC_000006.12:g.111515282dup, NC_000006.12:g.111515281_111515282dup, NC_000006.12:g.111515280_111515282dup, NC_000006.12:g.111515279_111515282dup, NC_000006.12:g.111515278_111515282dup, NC_000006.12:g.111515277_111515282dup, NC_000006.12:g.111515276_111515282dup, NC_000006.12:g.111515266_111515282dup, NC_000006.12:g.111515282_111515283insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.111515282_111515283insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.111836474_111836485del, NC_000006.11:g.111836475_111836485del, NC_000006.11:g.111836478_111836485del, NC_000006.11:g.111836480_111836485del, NC_000006.11:g.111836481_111836485del, NC_000006.11:g.111836482_111836485del, NC_000006.11:g.111836483_111836485del, NC_000006.11:g.111836484_111836485del, NC_000006.11:g.111836485del, NC_000006.11:g.111836485dup, NC_000006.11:g.111836484_111836485dup, NC_000006.11:g.111836483_111836485dup, NC_000006.11:g.111836482_111836485dup, NC_000006.11:g.111836481_111836485dup, NC_000006.11:g.111836480_111836485dup, NC_000006.11:g.111836479_111836485dup, NC_000006.11:g.111836469_111836485dup, NC_000006.11:g.111836485_111836486insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.111836485_111836486insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149138200911.

rs1491382009 has merged into rs1181462469 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:111534992 (GRCh38)
6:111856195 (GRCh37)
Canonical SPDI:: NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:111534977:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: TRAF3IP2-AS1 (Varview), LOC107986522 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000006.12:g.111534992_111535005del, NC_000006.12:g.111534993_111535005del, NC_000006.12:g.111534994_111535005del, NC_000006.12:g.111534995_111535005del, NC_000006.12:g.111534996_111535005del, NC_000006.12:g.111534997_111535005del, NC_000006.12:g.111534998_111535005del, NC_000006.12:g.111534999_111535005del, NC_000006.12:g.111535000_111535005del, NC_000006.12:g.111535001_111535005del, NC_000006.12:g.111535002_111535005del, NC_000006.12:g.111535003_111535005del, NC_000006.12:g.111535004_111535005del, NC_000006.12:g.111535005del, NC_000006.12:g.111535005dup, NC_000006.12:g.111535004_111535005dup, NC_000006.12:g.111535003_111535005dup, NC_000006.12:g.111535002_111535005dup, NC_000006.12:g.111535001_111535005dup, NC_000006.12:g.111535000_111535005dup, NC_000006.12:g.111534999_111535005dup, NC_000006.12:g.111534998_111535005dup, NC_000006.12:g.111534997_111535005dup, NC_000006.12:g.111534996_111535005dup, NC_000006.12:g.111534995_111535005dup, NC_000006.12:g.111534985_111535005dup, NC_000006.12:g.111534984_111535005dup, NC_000006.12:g.111534981_111535005dup, NC_000006.12:g.111534979_111535005dup, NC_000006.12:g.111534978_111535005dup, NC_000006.12:g.111535005_111535006insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.111535005_111535006insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.111856195_111856208del, NC_000006.11:g.111856196_111856208del, NC_000006.11:g.111856197_111856208del, NC_000006.11:g.111856198_111856208del, NC_000006.11:g.111856199_111856208del, NC_000006.11:g.111856200_111856208del, NC_000006.11:g.111856201_111856208del, NC_000006.11:g.111856202_111856208del, NC_000006.11:g.111856203_111856208del, NC_000006.11:g.111856204_111856208del, NC_000006.11:g.111856205_111856208del, NC_000006.11:g.111856206_111856208del, NC_000006.11:g.111856207_111856208del, NC_000006.11:g.111856208del, NC_000006.11:g.111856208dup, NC_000006.11:g.111856207_111856208dup, NC_000006.11:g.111856206_111856208dup, NC_000006.11:g.111856205_111856208dup, NC_000006.11:g.111856204_111856208dup, NC_000006.11:g.111856203_111856208dup, NC_000006.11:g.111856202_111856208dup, NC_000006.11:g.111856201_111856208dup, NC_000006.11:g.111856200_111856208dup, NC_000006.11:g.111856199_111856208dup, NC_000006.11:g.111856198_111856208dup, NC_000006.11:g.111856188_111856208dup, NC_000006.11:g.111856187_111856208dup, NC_000006.11:g.111856184_111856208dup, NC_000006.11:g.111856182_111856208dup, NC_000006.11:g.111856181_111856208dup, NC_000006.11:g.111856208_111856209insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.111856208_111856209insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149137984612.

rs1491379846 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GCC [Show Flanks]
Chromosome:: 6:111520958 (GRCh38)
6:111842162 (GRCh37)
Canonical SPDI:: NC_000006.12:111520958:CC:CCGCC
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: CCGCC=0./0 (ALFA)
CCG=0.000008/1 (GnomAD)
HGVS:: NC_000006.12:g.111520960_111520961insGCC, NC_000006.11:g.111842163_111842164insGCC

Select item 149137794913.

rs1491377949 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 6:111534977 (GRCh38)
6:111856180 (GRCh37)
Canonical SPDI:: NC_000006.12:111534976:GT:
Gene:: TRAF3IP2-AS1 (Varview), LOC107986522 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,genic_downstream_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000006.12:g.111534977_111534978del, NC_000006.11:g.111856180_111856181del

Select item 149136798014.

rs1491367980 has merged into rs529040872 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:111579326 (GRCh38)
6:111900529 (GRCh37)
Canonical SPDI:: NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:111579316:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: TRAF3IP2 (Varview), TRAF3IP2-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
-=0.0446/172 (ALSPAC)
HGVS:: NC_000006.12:g.111579326_111579340del, NC_000006.12:g.111579327_111579340del, NC_000006.12:g.111579328_111579340del, NC_000006.12:g.111579329_111579340del, NC_000006.12:g.111579330_111579340del, NC_000006.12:g.111579331_111579340del, NC_000006.12:g.111579332_111579340del, NC_000006.12:g.111579333_111579340del, NC_000006.12:g.111579334_111579340del, NC_000006.12:g.111579335_111579340del, NC_000006.12:g.111579336_111579340del, NC_000006.12:g.111579337_111579340del, NC_000006.12:g.111579338_111579340del, NC_000006.12:g.111579339_111579340del, NC_000006.12:g.111579340del, NC_000006.12:g.111579340dup, NC_000006.12:g.111579339_111579340dup, NC_000006.12:g.111579338_111579340dup, NC_000006.12:g.111579337_111579340dup, NC_000006.12:g.111579336_111579340dup, NC_000006.12:g.111579335_111579340dup, NC_000006.12:g.111579334_111579340dup, NC_000006.12:g.111579333_111579340dup, NC_000006.12:g.111579331_111579340dup, NC_000006.12:g.111579330_111579340dup, NC_000006.12:g.111579321_111579340dup, NC_000006.12:g.111579317_111579340dup, NC_000006.12:g.111579340_111579341insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.111579340_111579341insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.111579340_111579341insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.111579340_111579341insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.111900529_111900543del, NC_000006.11:g.111900530_111900543del, NC_000006.11:g.111900531_111900543del, NC_000006.11:g.111900532_111900543del, NC_000006.11:g.111900533_111900543del, NC_000006.11:g.111900534_111900543del, NC_000006.11:g.111900535_111900543del, NC_000006.11:g.111900536_111900543del, NC_000006.11:g.111900537_111900543del, NC_000006.11:g.111900538_111900543del, NC_000006.11:g.111900539_111900543del, NC_000006.11:g.111900540_111900543del, NC_000006.11:g.111900541_111900543del, NC_000006.11:g.111900542_111900543del, NC_000006.11:g.111900543del, NC_000006.11:g.111900543dup, NC_000006.11:g.111900542_111900543dup, NC_000006.11:g.111900541_111900543dup, NC_000006.11:g.111900540_111900543dup, NC_000006.11:g.111900539_111900543dup, NC_000006.11:g.111900538_111900543dup, NC_000006.11:g.111900537_111900543dup, NC_000006.11:g.111900536_111900543dup, NC_000006.11:g.111900534_111900543dup, NC_000006.11:g.111900533_111900543dup, NC_000006.11:g.111900524_111900543dup, NC_000006.11:g.111900520_111900543dup, NC_000006.11:g.111900543_111900544insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.111900543_111900544insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.111900543_111900544insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.111900543_111900544insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_032030.2:g.31548_31562del, NG_032030.2:g.31549_31562del, NG_032030.2:g.31550_31562del, NG_032030.2:g.31551_31562del, NG_032030.2:g.31552_31562del, NG_032030.2:g.31553_31562del, NG_032030.2:g.31554_31562del, NG_032030.2:g.31555_31562del, NG_032030.2:g.31556_31562del, NG_032030.2:g.31557_31562del, NG_032030.2:g.31558_31562del, NG_032030.2:g.31559_31562del, NG_032030.2:g.31560_31562del, NG_032030.2:g.31561_31562del, NG_032030.2:g.31562del, NG_032030.2:g.31562dup, NG_032030.2:g.31561_31562dup, NG_032030.2:g.31560_31562dup, NG_032030.2:g.31559_31562dup, NG_032030.2:g.31558_31562dup, NG_032030.2:g.31557_31562dup, NG_032030.2:g.31556_31562dup, NG_032030.2:g.31555_31562dup, NG_032030.2:g.31553_31562dup, NG_032030.2:g.31552_31562dup, NG_032030.2:g.31543_31562dup, NG_032030.2:g.31539_31562dup, NG_032030.2:g.31562_31563insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032030.2:g.31562_31563insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032030.2:g.31562_31563insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032030.2:g.31562_31563insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149134458115.

rs1491344581 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 6:111520970 (GRCh38)
6:111842174 (GRCh37)
Canonical SPDI:: NC_000006.12:111520970:G:GG
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
G=0.000008/1 (GnomAD)
HGVS:: NC_000006.12:g.111520971dup, NC_000006.11:g.111842174dup

Select item 149133692516.

rs1491336925 has merged into rs1331416962 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>-,TT [Show Flanks]
Chromosome:: 6:111553936 (GRCh38)
6:111875139 (GRCh37)
Canonical SPDI:: NC_000006.12:111553935:TTTTTTTT:TTTTTTT,NC_000006.12:111553935:TTTTTTTT:TTTTTTTTT
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.00004/1 (TOMMO)
HGVS:: NC_000006.12:g.111553943del, NC_000006.12:g.111553943dup, NC_000006.11:g.111875146del, NC_000006.11:g.111875146dup, NG_032030.2:g.56943del, NG_032030.2:g.56943dup, NG_053806.1:g.3559del, NG_053806.1:g.3559dup

Select item 149127865017.

rs1491278650 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 6:111544595 (GRCh38)
6:111865799 (GRCh37)
Canonical SPDI:: NC_000006.12:111544595:C:CC
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by cluster
HGVS:: NC_000006.12:g.111544596dup, NC_000006.11:g.111865799dup

Select item 149127493918.

rs1491274939 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:111579316 (GRCh38)
6:111900519 (GRCh37)
Canonical SPDI:: NC_000006.12:111579315:CA:
Gene:: TRAF3IP2 (Varview), TRAF3IP2-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.0145/172 (ALFA)
-=0.00092/35 (GnomAD)
-=0.01115/186 (TOMMO)
HGVS:: NC_000006.12:g.111579316_111579317del, NC_000006.11:g.111900519_111900520del, NG_032030.2:g.31562_31563del

Select item 149124797219.

rs1491247972 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 6:111520960 (GRCh38)
6:111842164 (GRCh37)
Canonical SPDI:: NC_000006.12:111520960::G
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000182/4 (GnomAD)
HGVS:: NC_000006.12:g.111520960_111520961insG, NC_000006.11:g.111842163_111842164insG

Select item 149123673820.

rs1491236738 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:111515261 (GRCh38)
6:111836464 (GRCh37)
Canonical SPDI:: NC_000006.12:111515260:CA:
Gene:: TRAF3IP2-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000006.12:g.111515261_111515262del, NC_000006.11:g.111836464_111836465del

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