SNP Links for Nucleotide (Select 588480542) - SNP

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Select item 14915777701.

rs1491577770 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 22:21835533 (GRCh38)
22:22189823 (GRCh37)
Canonical SPDI:: NC_000022.11:21835533:G:GG
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.21835534dup, NC_000022.10:g.22189823dup, NG_023054.2:g.37147dup

Select item 14915719862.

rs1491571986 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 22:21814855 (GRCh38)
22:22169145 (GRCh37)
Canonical SPDI:: NC_000022.11:21814855::C
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000022.11:g.21814855_21814856insC, NC_000022.10:g.22169144_22169145insC, NG_023054.2:g.57825_57826insG

Select item 14915534063.

rs1491553406 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,AA,AAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 22:21848437 (GRCh38)
22:22202727 (GRCh37)
Canonical SPDI:: NC_000022.11:21848437::A,NC_000022.11:21848437::AA,NC_000022.11:21848437::AAA,NC_000022.11:21848437::AAAAA,NC_000022.11:21848437::AAAAAA,NC_000022.11:21848437::AAAAAAAA,NC_000022.11:21848437::AAAAAAAAA,NC_000022.11:21848437::AAAAAAAAAAAAAAAAAAAAA
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
AA=0.00029/8 (TOMMO)
HGVS:: NC_000022.11:g.21848437_21848438insA, NC_000022.11:g.21848437_21848438insAA, NC_000022.11:g.21848437_21848438insAAA, NC_000022.11:g.21848437_21848438insAAAAA, NC_000022.11:g.21848437_21848438insAAAAAA, NC_000022.11:g.21848437_21848438insAAAAAAAA, NC_000022.11:g.21848437_21848438insAAAAAAAAA, NC_000022.11:g.21848437_21848438insAAAAAAAAAAAAAAAAAAAAA, NC_000022.10:g.22202726_22202727insA, NC_000022.10:g.22202726_22202727insAA, NC_000022.10:g.22202726_22202727insAAA, NC_000022.10:g.22202726_22202727insAAAAA, NC_000022.10:g.22202726_22202727insAAAAAA, NC_000022.10:g.22202726_22202727insAAAAAAAA, NC_000022.10:g.22202726_22202727insAAAAAAAAA, NC_000022.10:g.22202726_22202727insAAAAAAAAAAAAAAAAAAAAA, NG_023054.2:g.24243_24244insT, NG_023054.2:g.24243_24244insTT, NG_023054.2:g.24243_24244insTTT, NG_023054.2:g.24243_24244insTTTTT, NG_023054.2:g.24243_24244insTTTTTT, NG_023054.2:g.24243_24244insTTTTTTTT, NG_023054.2:g.24243_24244insTTTTTTTTT, NG_023054.2:g.24243_24244insTTTTTTTTTTTTTTTTTTTTT

Select item 14915478064.

rs1491547806 has merged into rs377191296 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT [Show Flanks]
Chromosome:: 22:21840836 (GRCh38)
22:22195125 (GRCh37)
Canonical SPDI:: NC_000022.11:21840826:TTTTTTTTTTTTTT:TTTTTTTTT,NC_000022.11:21840826:TTTTTTTTTTTTTT:TTTTTTTTTT,NC_000022.11:21840826:TTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000022.11:21840826:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000022.11:21840826:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000022.11:21840826:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000022.11:21840826:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000022.11:21840826:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
-=0.045/27 (NorthernSweden)
-=0.15974/800 (1000Genomes)
HGVS:: NC_000022.11:g.21840836_21840840del, NC_000022.11:g.21840837_21840840del, NC_000022.11:g.21840838_21840840del, NC_000022.11:g.21840839_21840840del, NC_000022.11:g.21840840del, NC_000022.11:g.21840840dup, NC_000022.11:g.21840839_21840840dup, NC_000022.11:g.21840838_21840840dup, NC_000022.10:g.22195125_22195129del, NC_000022.10:g.22195126_22195129del, NC_000022.10:g.22195127_22195129del, NC_000022.10:g.22195128_22195129del, NC_000022.10:g.22195129del, NC_000022.10:g.22195129dup, NC_000022.10:g.22195128_22195129dup, NC_000022.10:g.22195127_22195129dup, NG_023054.2:g.31850_31854del, NG_023054.2:g.31851_31854del, NG_023054.2:g.31852_31854del, NG_023054.2:g.31853_31854del, NG_023054.2:g.31854del, NG_023054.2:g.31854dup, NG_023054.2:g.31853_31854dup, NG_023054.2:g.31852_31854dup

Select item 14915316445.

rs1491531644 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 22:21814854 (GRCh38)
22:22169143 (GRCh37)
Canonical SPDI:: NC_000022.11:21814852:ACA:A
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.00007/1 (TOMMO)
-=0.00036/26 (GnomAD)
HGVS:: NC_000022.11:g.21814854_21814855del, NC_000022.10:g.22169143_22169144del, NG_023054.2:g.57827_57828del

Select item 14915197576.

rs1491519757 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 22:21849318 (GRCh38)
22:22203607 (GRCh37)
Canonical SPDI:: NC_000022.11:21849317:CA:
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000022.11:g.21849318_21849319del, NC_000022.10:g.22203607_22203608del, NG_023054.2:g.23362_23363del

Select item 14915123917.

rs1491512391 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 22:21773266 (GRCh38)
22:22127555 (GRCh37)
Canonical SPDI:: NC_000022.11:21773265:TG:
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00042/5 (ALFA)
-=0.00168/47 (TOMMO)
HGVS:: NC_000022.11:g.21773266_21773267del, NC_000022.10:g.22127555_22127556del, NG_023054.2:g.99414_99415del

Select item 14914746828.

rs1491474682 has merged into rs11303516 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 22:21851653 (GRCh38)
22:22205942 (GRCh37)
Canonical SPDI:: NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21851643:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.000015/4 (TOPMED)
-=0.35024/1754 (1000Genomes)
HGVS:: NC_000022.11:g.21851653_21851665del, NC_000022.11:g.21851655_21851665del, NC_000022.11:g.21851656_21851665del, NC_000022.11:g.21851657_21851665del, NC_000022.11:g.21851658_21851665del, NC_000022.11:g.21851659_21851665del, NC_000022.11:g.21851661_21851665del, NC_000022.11:g.21851662_21851665del, NC_000022.11:g.21851663_21851665del, NC_000022.11:g.21851664_21851665del, NC_000022.11:g.21851665del, NC_000022.11:g.21851665dup, NC_000022.11:g.21851664_21851665dup, NC_000022.11:g.21851663_21851665dup, NC_000022.11:g.21851662_21851665dup, NC_000022.11:g.21851661_21851665dup, NC_000022.11:g.21851660_21851665dup, NC_000022.11:g.21851659_21851665dup, NC_000022.11:g.21851655_21851665dup, NC_000022.11:g.21851645_21851665dup, NC_000022.10:g.22205942_22205954del, NC_000022.10:g.22205944_22205954del, NC_000022.10:g.22205945_22205954del, NC_000022.10:g.22205946_22205954del, NC_000022.10:g.22205947_22205954del, NC_000022.10:g.22205948_22205954del, NC_000022.10:g.22205950_22205954del, NC_000022.10:g.22205951_22205954del, NC_000022.10:g.22205952_22205954del, NC_000022.10:g.22205953_22205954del, NC_000022.10:g.22205954del, NC_000022.10:g.22205954dup, NC_000022.10:g.22205953_22205954dup, NC_000022.10:g.22205952_22205954dup, NC_000022.10:g.22205951_22205954dup, NC_000022.10:g.22205950_22205954dup, NC_000022.10:g.22205949_22205954dup, NC_000022.10:g.22205948_22205954dup, NC_000022.10:g.22205944_22205954dup, NC_000022.10:g.22205934_22205954dup, NG_023054.2:g.21025_21037del, NG_023054.2:g.21027_21037del, NG_023054.2:g.21028_21037del, NG_023054.2:g.21029_21037del, NG_023054.2:g.21030_21037del, NG_023054.2:g.21031_21037del, NG_023054.2:g.21033_21037del, NG_023054.2:g.21034_21037del, NG_023054.2:g.21035_21037del, NG_023054.2:g.21036_21037del, NG_023054.2:g.21037del, NG_023054.2:g.21037dup, NG_023054.2:g.21036_21037dup, NG_023054.2:g.21035_21037dup, NG_023054.2:g.21034_21037dup, NG_023054.2:g.21033_21037dup, NG_023054.2:g.21032_21037dup, NG_023054.2:g.21031_21037dup, NG_023054.2:g.21027_21037dup, NG_023054.2:g.21017_21037dup

Select item 14914494029.

rs1491449402 has merged into rs1350380577 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA [Show Flanks]
Chromosome:: 22:21778361 (GRCh38)
22:22132650 (GRCh37)
Canonical SPDI:: NC_000022.11:21778350:AAAAAAAAAAAAAA:AAAAAAAAAA,NC_000022.11:21778350:AAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000022.11:21778350:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000022.11:21778350:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000022.11:21778350:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000022.11:21778350:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000022.11:21778350:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000022.11:21778350:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000022.11:21778350:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
A=0.0068/74 (TOMMO)
HGVS:: NC_000022.11:g.21778361_21778364del, NC_000022.11:g.21778362_21778364del, NC_000022.11:g.21778363_21778364del, NC_000022.11:g.21778364del, NC_000022.11:g.21778364dup, NC_000022.11:g.21778363_21778364dup, NC_000022.11:g.21778361_21778364dup, NC_000022.11:g.21778360_21778364dup, NC_000022.11:g.21778359_21778364dup, NC_000022.10:g.22132650_22132653del, NC_000022.10:g.22132651_22132653del, NC_000022.10:g.22132652_22132653del, NC_000022.10:g.22132653del, NC_000022.10:g.22132653dup, NC_000022.10:g.22132652_22132653dup, NC_000022.10:g.22132650_22132653dup, NC_000022.10:g.22132649_22132653dup, NC_000022.10:g.22132648_22132653dup, NG_023054.2:g.94327_94330del, NG_023054.2:g.94328_94330del, NG_023054.2:g.94329_94330del, NG_023054.2:g.94330del, NG_023054.2:g.94330dup, NG_023054.2:g.94329_94330dup, NG_023054.2:g.94327_94330dup, NG_023054.2:g.94326_94330dup, NG_023054.2:g.94325_94330dup

Select item 149143758610.

rs1491437586 has merged into rs1188846394 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGA>-,GA,GAGAGA,GAGAGACAGAGAGAGA,GAGAGAGA,GAGAGAGAGA,GAGAGAGAGAGA,GAGAGAGAGAGAGA,GAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGA [Show Flanks]
Chromosome:: 22:21814850 (GRCh38)
22:22169139 (GRCh37)
Canonical SPDI:: NC_000022.11:21814845:GAGAGAGA:GAGA,NC_000022.11:21814845:GAGAGAGA:GAGAGA,NC_000022.11:21814845:GAGAGAGA:GAGAGAGAGA,NC_000022.11:21814845:GAGAGAGA:GAGAGAGAGACAGAGAGAGA,NC_000022.11:21814845:GAGAGAGA:GAGAGAGAGAGA,NC_000022.11:21814845:GAGAGAGA:GAGAGAGAGAGAGA,NC_000022.11:21814845:GAGAGAGA:GAGAGAGAGAGAGAGA,NC_000022.11:21814845:GAGAGAGA:GAGAGAGAGAGAGAGAGA,NC_000022.11:21814845:GAGAGAGA:GAGAGAGAGAGAGAGAGAGA,NC_000022.11:21814845:GAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGA,NC_000022.11:21814845:GAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGA
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAGAGA=0./0 (ALFA)
HGVS:: NC_000022.11:g.21814846GA[2], NC_000022.11:g.21814846GA[3], NC_000022.11:g.21814846GA[5], NC_000022.11:g.21814846_21814853GA[5]CAGAGAGAGA[1], NC_000022.11:g.21814846GA[6], NC_000022.11:g.21814846GA[7], NC_000022.11:g.21814846GA[8], NC_000022.11:g.21814846GA[9], NC_000022.11:g.21814846GA[10], NC_000022.11:g.21814846GA[12], NC_000022.11:g.21814846GA[13], NC_000022.10:g.22169135GA[2], NC_000022.10:g.22169135GA[3], NC_000022.10:g.22169135GA[5], NC_000022.10:g.22169135_22169142GA[5]CAGAGAGAGA[1], NC_000022.10:g.22169135GA[6], NC_000022.10:g.22169135GA[7], NC_000022.10:g.22169135GA[8], NC_000022.10:g.22169135GA[9], NC_000022.10:g.22169135GA[10], NC_000022.10:g.22169135GA[12], NC_000022.10:g.22169135GA[13], NG_023054.2:g.57828TC[2], NG_023054.2:g.57828TC[3], NG_023054.2:g.57828TC[5], NG_023054.2:g.57828_57835TC[4]TGTCTCTCTCTC[1], NG_023054.2:g.57828TC[6], NG_023054.2:g.57828TC[7], NG_023054.2:g.57828TC[8], NG_023054.2:g.57828TC[9], NG_023054.2:g.57828TC[10], NG_023054.2:g.57828TC[12], NG_023054.2:g.57828TC[13]

Select item 149142270211.

rs1491422702 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 22:21851643 (GRCh38)
22:22205932 (GRCh37)
Canonical SPDI:: NC_000022.11:21851642:CA:
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00017/2 (ALFA)
HGVS:: NC_000022.11:g.21851643_21851644del, NC_000022.10:g.22205932_22205933del, NG_023054.2:g.21037_21038del

Select item 149140755012.

rs1491407550 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 22:21871495 (GRCh38)
22:22225786 (GRCh37)
Canonical SPDI:: NC_000022.11:21871495::A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000022.11:g.21871495_21871496insA, NC_000022.10:g.22225785_22225786insA, NG_023054.2:g.1185_1186insT

Select item 149140409913.

rs1491404099 has merged into rs36031460 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA [Show Flanks]
Chromosome:: 22:21853344 (GRCh38)
22:22207633 (GRCh37)
Canonical SPDI:: NC_000022.11:21853331:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000022.11:21853331:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000022.11:21853331:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000022.11:21853331:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000022.11:21853331:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000022.11:21853331:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000022.11:21853331:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000022.11:21853331:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000022.11:21853331:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21853331:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21853331:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.0963/371 (ALSPAC)
-=0.325/13 (GENOME_DK)
HGVS:: NC_000022.11:g.21853344_21853348del, NC_000022.11:g.21853345_21853348del, NC_000022.11:g.21853346_21853348del, NC_000022.11:g.21853347_21853348del, NC_000022.11:g.21853348del, NC_000022.11:g.21853348dup, NC_000022.11:g.21853347_21853348dup, NC_000022.11:g.21853346_21853348dup, NC_000022.11:g.21853344_21853348dup, NC_000022.11:g.21853343_21853348dup, NC_000022.11:g.21853342_21853348dup, NC_000022.10:g.22207633_22207637del, NC_000022.10:g.22207634_22207637del, NC_000022.10:g.22207635_22207637del, NC_000022.10:g.22207636_22207637del, NC_000022.10:g.22207637del, NC_000022.10:g.22207637dup, NC_000022.10:g.22207636_22207637dup, NC_000022.10:g.22207635_22207637dup, NC_000022.10:g.22207633_22207637dup, NC_000022.10:g.22207632_22207637dup, NC_000022.10:g.22207631_22207637dup, NG_023054.2:g.19345_19349del, NG_023054.2:g.19346_19349del, NG_023054.2:g.19347_19349del, NG_023054.2:g.19348_19349del, NG_023054.2:g.19349del, NG_023054.2:g.19349dup, NG_023054.2:g.19348_19349dup, NG_023054.2:g.19347_19349dup, NG_023054.2:g.19345_19349dup, NG_023054.2:g.19344_19349dup, NG_023054.2:g.19343_19349dup

Select item 149139911514.

rs1491399115 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 22:21774714 (GRCh38)
22:22129003 (GRCh37)
Canonical SPDI:: NC_000022.11:21774713:CA:
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00228/27 (ALFA)
-=0.00093/25 (TOMMO)
HGVS:: NC_000022.11:g.21774714_21774715del, NC_000022.10:g.22129003_22129004del, NG_023054.2:g.97966_97967del

Select item 149138289315.

rs1491382893 has merged into rs66777137 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 22:21871503 (GRCh38)
22:22225793 (GRCh37)
Canonical SPDI:: NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000022.11:21871494:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
HGVS:: NC_000022.11:g.21871503_21871516del, NC_000022.11:g.21871504_21871516del, NC_000022.11:g.21871505_21871516del, NC_000022.11:g.21871506_21871516del, NC_000022.11:g.21871507_21871516del, NC_000022.11:g.21871508_21871516del, NC_000022.11:g.21871509_21871516del, NC_000022.11:g.21871510_21871516del, NC_000022.11:g.21871511_21871516del, NC_000022.11:g.21871512_21871516del, NC_000022.11:g.21871513_21871516del, NC_000022.11:g.21871514_21871516del, NC_000022.11:g.21871515_21871516del, NC_000022.11:g.21871516del, NC_000022.11:g.21871516dup, NC_000022.11:g.21871515_21871516dup, NC_000022.11:g.21871514_21871516dup, NC_000022.11:g.21871513_21871516dup, NC_000022.11:g.21871499_21871516dup, NC_000022.11:g.21871498_21871516dup, NC_000022.11:g.21871516_21871517insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000022.11:g.21871516_21871517insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000022.11:g.21871516_21871517insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000022.11:g.21871516_21871517insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000022.10:g.22225793_22225806del, NC_000022.10:g.22225794_22225806del, NC_000022.10:g.22225795_22225806del, NC_000022.10:g.22225796_22225806del, NC_000022.10:g.22225797_22225806del, NC_000022.10:g.22225798_22225806del, NC_000022.10:g.22225799_22225806del, NC_000022.10:g.22225800_22225806del, NC_000022.10:g.22225801_22225806del, NC_000022.10:g.22225802_22225806del, NC_000022.10:g.22225803_22225806del, NC_000022.10:g.22225804_22225806del, NC_000022.10:g.22225805_22225806del, NC_000022.10:g.22225806del, NC_000022.10:g.22225806dup, NC_000022.10:g.22225805_22225806dup, NC_000022.10:g.22225804_22225806dup, NC_000022.10:g.22225803_22225806dup, NC_000022.10:g.22225789_22225806dup, NC_000022.10:g.22225788_22225806dup, NC_000022.10:g.22225806_22225807insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000022.10:g.22225806_22225807insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000022.10:g.22225806_22225807insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000022.10:g.22225806_22225807insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_023054.2:g.1173_1186del, NG_023054.2:g.1174_1186del, NG_023054.2:g.1175_1186del, NG_023054.2:g.1176_1186del, NG_023054.2:g.1177_1186del, NG_023054.2:g.1178_1186del, NG_023054.2:g.1179_1186del, NG_023054.2:g.1180_1186del, NG_023054.2:g.1181_1186del, NG_023054.2:g.1182_1186del, NG_023054.2:g.1183_1186del, NG_023054.2:g.1184_1186del, NG_023054.2:g.1185_1186del, NG_023054.2:g.1186del, NG_023054.2:g.1186dup, NG_023054.2:g.1185_1186dup, NG_023054.2:g.1184_1186dup, NG_023054.2:g.1183_1186dup, NG_023054.2:g.1169_1186dup, NG_023054.2:g.1168_1186dup, NG_023054.2:g.1186_1187insAAAAAAAAAAAAAAAAAAAAAAAA, NG_023054.2:g.1186_1187insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_023054.2:g.1186_1187insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_023054.2:g.1186_1187insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149137185716.

rs1491371857 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GA [Show Flanks]
Chromosome:: 22:21830517 (GRCh38)
22:22184807 (GRCh37)
Canonical SPDI:: NC_000022.11:21830517:A:AGA
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AGA=0./0 (ALFA)
AG=0.000029/3 (GnomAD)
HGVS:: NC_000022.11:g.21830518_21830519insGA, NC_000022.10:g.22184807_22184808insGA, NG_023054.2:g.42163_42164insCT

Select item 149137079017.

rs1491370790 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 22:21778607 (GRCh38)
22:22132896 (GRCh37)
Canonical SPDI:: NC_000022.11:21778606:AG:
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00003/1 (GnomAD)
HGVS:: NC_000022.11:g.21778607_21778608del, NC_000022.10:g.22132896_22132897del, NG_023054.2:g.94073_94074del

Select item 149136999418.

rs1491369994 [Homo sapiens]

Variant type:: DELINS
Alleles:: CAGAGAGA>-,CAGAGAGACAGAGAGA,CAGAGAGACAGAGAGACAGAGAGA [Show Flanks]
Chromosome:: 22:21814854 (GRCh38)
22:22169143 (GRCh37)
Canonical SPDI:: NC_000022.11:21814846:AGAGAGACAGAGAGA:AGAGAGA,NC_000022.11:21814846:AGAGAGACAGAGAGA:AGAGAGACAGAGAGACAGAGAGA,NC_000022.11:21814846:AGAGAGACAGAGAGA:AGAGAGACAGAGAGACAGAGAGACAGAGAGA
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAGAGACAGAGAGACAGAGAGA=0./0 (ALFA)
HGVS:: NC_000022.11:g.21814854_21814861del, NC_000022.11:g.21814854_21814861dup, NC_000022.11:g.21814854CAGAGAGA[3], NC_000022.10:g.22169143_22169150del, NC_000022.10:g.22169143_22169150dup, NC_000022.10:g.22169143CAGAGAGA[3], NG_023054.2:g.57827_57834del, NG_023054.2:g.57827_57834dup, NG_023054.2:g.57827GTCTCTCT[3]

Select item 149134915419.

rs1491349154 has merged into rs56973202 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAAAAAA>-,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 22:21774718 (GRCh38)
22:22129007 (GRCh37)
Canonical SPDI:: NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000022.11:21774714:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000022.11:g.21774718_21774739del, NC_000022.11:g.21774724_21774739del, NC_000022.11:g.21774726_21774739del, NC_000022.11:g.21774727_21774739del, NC_000022.11:g.21774728_21774739del, NC_000022.11:g.21774729_21774739del, NC_000022.11:g.21774730_21774739del, NC_000022.11:g.21774732_21774739del, NC_000022.11:g.21774733_21774739del, NC_000022.11:g.21774734_21774739del, NC_000022.11:g.21774735_21774739del, NC_000022.11:g.21774736_21774739del, NC_000022.11:g.21774737_21774739del, NC_000022.11:g.21774738_21774739del, NC_000022.11:g.21774739del, NC_000022.11:g.21774739dup, NC_000022.11:g.21774738_21774739dup, NC_000022.11:g.21774737_21774739dup, NC_000022.11:g.21774736_21774739dup, NC_000022.11:g.21774735_21774739dup, NC_000022.11:g.21774734_21774739dup, NC_000022.11:g.21774733_21774739dup, NC_000022.11:g.21774732_21774739dup, NC_000022.11:g.21774722_21774739dup, NC_000022.11:g.21774739_21774740insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000022.10:g.22129007_22129028del, NC_000022.10:g.22129013_22129028del, NC_000022.10:g.22129015_22129028del, NC_000022.10:g.22129016_22129028del, NC_000022.10:g.22129017_22129028del, NC_000022.10:g.22129018_22129028del, NC_000022.10:g.22129019_22129028del, NC_000022.10:g.22129021_22129028del, NC_000022.10:g.22129022_22129028del, NC_000022.10:g.22129023_22129028del, NC_000022.10:g.22129024_22129028del, NC_000022.10:g.22129025_22129028del, NC_000022.10:g.22129026_22129028del, NC_000022.10:g.22129027_22129028del, NC_000022.10:g.22129028del, NC_000022.10:g.22129028dup, NC_000022.10:g.22129027_22129028dup, NC_000022.10:g.22129026_22129028dup, NC_000022.10:g.22129025_22129028dup, NC_000022.10:g.22129024_22129028dup, NC_000022.10:g.22129023_22129028dup, NC_000022.10:g.22129022_22129028dup, NC_000022.10:g.22129021_22129028dup, NC_000022.10:g.22129011_22129028dup, NC_000022.10:g.22129028_22129029insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_023054.2:g.97945_97966del, NG_023054.2:g.97951_97966del, NG_023054.2:g.97953_97966del, NG_023054.2:g.97954_97966del, NG_023054.2:g.97955_97966del, NG_023054.2:g.97956_97966del, NG_023054.2:g.97957_97966del, NG_023054.2:g.97959_97966del, NG_023054.2:g.97960_97966del, NG_023054.2:g.97961_97966del, NG_023054.2:g.97962_97966del, NG_023054.2:g.97963_97966del, NG_023054.2:g.97964_97966del, NG_023054.2:g.97965_97966del, NG_023054.2:g.97966del, NG_023054.2:g.97966dup, NG_023054.2:g.97965_97966dup, NG_023054.2:g.97964_97966dup, NG_023054.2:g.97963_97966dup, NG_023054.2:g.97962_97966dup, NG_023054.2:g.97961_97966dup, NG_023054.2:g.97960_97966dup, NG_023054.2:g.97959_97966dup, NG_023054.2:g.97949_97966dup, NG_023054.2:g.97966_97967insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149130918020.

rs1491309180 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 22:21834574 (GRCh38)
22:22188863 (GRCh37)
Canonical SPDI:: NC_000022.11:21834572:TAT:T
Gene:: MAPK1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.00051/6 (ALFA)
HGVS:: NC_000022.11:g.21834574_21834575del, NC_000022.10:g.22188863_22188864del, NG_023054.2:g.38107_38108del

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