SNP Links for Nucleotide (Select 211904120) - SNP

Links from Nucleotide

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Select item 14915203581.

rs1491520358 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TATT [Show Flanks]
Chromosome:: 11:64812843 (GRCh38)
11:64580316 (GRCh37)
Canonical SPDI:: NC_000011.10:64812843:ATT:ATTTATT
Gene:: MEN1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: ATTTATT=0./0 (ALFA)
HGVS:: NC_000011.10:g.64812846_64812847insTATT, NC_000011.9:g.64580318_64580319insTATT, NG_008929.1:g.3451_3452insAAAT

Select item 14913366672.

rs1491336667 [Homo sapiens]

Variant type:: INS
Alleles:: ->C,CAC,CACAC,CACACAC,CACACACAC [Show Flanks]
Chromosome:: 11:64811304 (GRCh38)
11:64578777 (GRCh37)
Canonical SPDI:: NC_000011.10:64811304::C,NC_000011.10:64811304::CAC,NC_000011.10:64811304::CACAC,NC_000011.10:64811304::CACACAC,NC_000011.10:64811304::CACACACAC
Gene:: MEN1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACAC=0./0 (ALFA)
C=0.00558/10 (Korea1K)
HGVS:: NC_000011.10:g.64811304_64811305insC, NC_000011.10:g.64811304_64811305insCAC, NC_000011.10:g.64811304_64811305insCACAC, NC_000011.10:g.64811304_64811305insCACACAC, NC_000011.10:g.64811304_64811305insCACACACAC, NC_000011.9:g.64578776_64578777insC, NC_000011.9:g.64578776_64578777insCAC, NC_000011.9:g.64578776_64578777insCACAC, NC_000011.9:g.64578776_64578777insCACACAC, NC_000011.9:g.64578776_64578777insCACACACAC, NG_008929.1:g.4990_4991insG, NG_008929.1:g.4990_4991insGTG, NG_008929.1:g.4990_4991insGTGTG, NG_008929.1:g.4990_4991insGTGTGTG, NG_008929.1:g.4990_4991insGTGTGTGTG

Select item 14913112773.

rs1491311277 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 11:64811304 (GRCh38)
11:64578776 (GRCh37)
Canonical SPDI:: NC_000011.10:64811303:AA:
Gene:: MEN1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00025/3 (ALFA)
-=0.00052/45 (GnomAD)
HGVS:: NC_000011.10:g.64811304_64811305del, NC_000011.9:g.64578776_64578777del, NG_008929.1:g.4990_4991del

Select item 14913025474.

rs1491302547 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATA,ATATA,ATATATA,ATATATATA [Show Flanks]
Chromosome:: 11:64811356 (GRCh38)
11:64578829 (GRCh37)
Canonical SPDI:: NC_000011.10:64811356::A,NC_000011.10:64811356::ATA,NC_000011.10:64811356::ATATA,NC_000011.10:64811356::ATATATA,NC_000011.10:64811356::ATATATATA
Gene:: MEN1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: ATA=0./0 (ALFA)
A=0.00107/20 (TOMMO)
HGVS:: NC_000011.10:g.64811356_64811357insA, NC_000011.10:g.64811356_64811357insATA, NC_000011.10:g.64811356_64811357insATATA, NC_000011.10:g.64811356_64811357insATATATA, NC_000011.10:g.64811356_64811357insATATATATA, NC_000011.9:g.64578828_64578829insA, NC_000011.9:g.64578828_64578829insATA, NC_000011.9:g.64578828_64578829insATATA, NC_000011.9:g.64578828_64578829insATATATA, NC_000011.9:g.64578828_64578829insATATATATA, NG_008929.1:g.4938_4939insT, NG_008929.1:g.4938_4939insTAT, NG_008929.1:g.4938_4939insTATAT, NG_008929.1:g.4938_4939insTATATAT, NG_008929.1:g.4938_4939insTATATATAT

Select item 14912040845.

rs1491204084 has merged into rs869164525 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:64811365 (GRCh38)
11:64578837 (GRCh37)
Canonical SPDI:: NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:64811355:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: MEN1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Clinical significance:: benign,likely-benign
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000011.10:g.64811365_64811388del, NC_000011.10:g.64811367_64811388del, NC_000011.10:g.64811368_64811388del, NC_000011.10:g.64811369_64811388del, NC_000011.10:g.64811370_64811388del, NC_000011.10:g.64811371_64811388del, NC_000011.10:g.64811372_64811388del, NC_000011.10:g.64811373_64811388del, NC_000011.10:g.64811374_64811388del, NC_000011.10:g.64811375_64811388del, NC_000011.10:g.64811376_64811388del, NC_000011.10:g.64811377_64811388del, NC_000011.10:g.64811378_64811388del, NC_000011.10:g.64811379_64811388del, NC_000011.10:g.64811380_64811388del, NC_000011.10:g.64811381_64811388del, NC_000011.10:g.64811382_64811388del, NC_000011.10:g.64811383_64811388del, NC_000011.10:g.64811384_64811388del, NC_000011.10:g.64811385_64811388del, NC_000011.10:g.64811386_64811388del, NC_000011.10:g.64811387_64811388del, NC_000011.10:g.64811388del, NC_000011.10:g.64811388dup, NC_000011.10:g.64811387_64811388dup, NC_000011.10:g.64811386_64811388dup, NC_000011.10:g.64811385_64811388dup, NC_000011.10:g.64811384_64811388dup, NC_000011.10:g.64811383_64811388dup, NC_000011.10:g.64811382_64811388dup, NC_000011.9:g.64578837_64578860del, NC_000011.9:g.64578839_64578860del, NC_000011.9:g.64578840_64578860del, NC_000011.9:g.64578841_64578860del, NC_000011.9:g.64578842_64578860del, NC_000011.9:g.64578843_64578860del, NC_000011.9:g.64578844_64578860del, NC_000011.9:g.64578845_64578860del, NC_000011.9:g.64578846_64578860del, NC_000011.9:g.64578847_64578860del, NC_000011.9:g.64578848_64578860del, NC_000011.9:g.64578849_64578860del, NC_000011.9:g.64578850_64578860del, NC_000011.9:g.64578851_64578860del, NC_000011.9:g.64578852_64578860del, NC_000011.9:g.64578853_64578860del, NC_000011.9:g.64578854_64578860del, NC_000011.9:g.64578855_64578860del, NC_000011.9:g.64578856_64578860del, NC_000011.9:g.64578857_64578860del, NC_000011.9:g.64578858_64578860del, NC_000011.9:g.64578859_64578860del, NC_000011.9:g.64578860del, NC_000011.9:g.64578860dup, NC_000011.9:g.64578859_64578860dup, NC_000011.9:g.64578858_64578860dup, NC_000011.9:g.64578857_64578860dup, NC_000011.9:g.64578856_64578860dup, NC_000011.9:g.64578855_64578860dup, NC_000011.9:g.64578854_64578860dup, NG_008929.1:g.4916_4939del, NG_008929.1:g.4918_4939del, NG_008929.1:g.4919_4939del, NG_008929.1:g.4920_4939del, NG_008929.1:g.4921_4939del, NG_008929.1:g.4922_4939del, NG_008929.1:g.4923_4939del, NG_008929.1:g.4924_4939del, NG_008929.1:g.4925_4939del, NG_008929.1:g.4926_4939del, NG_008929.1:g.4927_4939del, NG_008929.1:g.4928_4939del, NG_008929.1:g.4929_4939del, NG_008929.1:g.4930_4939del, NG_008929.1:g.4931_4939del, NG_008929.1:g.4932_4939del, NG_008929.1:g.4933_4939del, NG_008929.1:g.4934_4939del, NG_008929.1:g.4935_4939del, NG_008929.1:g.4936_4939del, NG_008929.1:g.4937_4939del, NG_008929.1:g.4938_4939del, NG_008929.1:g.4939del, NG_008929.1:g.4939dup, NG_008929.1:g.4938_4939dup, NG_008929.1:g.4937_4939dup, NG_008929.1:g.4936_4939dup, NG_008929.1:g.4935_4939dup, NG_008929.1:g.4934_4939dup, NG_008929.1:g.4933_4939dup

Select item 14911661286.

rs1491166128 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 11:64812843 (GRCh38)
11:64580315 (GRCh37)
Canonical SPDI:: NC_000011.10:64812842:AA:
Gene:: MEN1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: -=0.000186/26 (GnomAD)
-=0.013187/24 (Korea1K)
-=0.019676/328 (TOMMO)
HGVS:: NC_000011.10:g.64812843_64812844del, NC_000011.9:g.64580315_64580316del, NG_008929.1:g.3451_3452del

Select item 14908665437.

rs1490866543 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:64810486 (GRCh38)
11:64577958 (GRCh37)
Canonical SPDI:: NC_000011.10:64810485:A:G,NC_000011.10:64810485:A:T
Gene:: MEN1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.64810486A>G, NC_000011.10:g.64810486A>T, NC_000011.9:g.64577958A>G, NC_000011.9:g.64577958A>T, NG_008929.1:g.5809T>C, NG_008929.1:g.5809T>A, NM_130802.3:c.-242T>C, NM_130802.3:c.-242T>A, NM_130802.2:c.-242T>C, NM_130802.2:c.-242T>A, NM_001370261.2:c.-242T>C, NM_001370261.2:c.-242T>A, NM_001370261.1:c.-242T>C, NM_001370261.1:c.-242T>A, NM_001370262.2:c.-242T>C, NM_001370262.2:c.-242T>A, NM_001370262.1:c.-242T>C, NM_001370262.1:c.-242T>A, NR_176287.1:n.66T>C, NR_176287.1:n.66T>A, NM_001407150.1:c.-242T>C, NM_001407150.1:c.-242T>A, NM_001407143.1:c.-242T>C, NM_001407143.1:c.-242T>A, NM_001407147.1:c.-215T>C, NM_001407147.1:c.-215T>A, NM_001407145.1:c.-52T>C, NM_001407145.1:c.-52T>A, NM_001407146.1:c.-52T>C, NM_001407146.1:c.-52T>A, XM_017017765.2:c.-242T>C, XM_017017765.2:c.-242T>A, XM_011545040.2:c.-242T>C, XM_011545040.2:c.-242T>A

Select item 14908205458.

rs1490820545 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:64802700 (GRCh38)
11:64570172 (GRCh37)
Canonical SPDI:: NC_000011.10:64802699:G:A
Gene:: MAP4K2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000011.10:g.64802700G>A, NC_000011.9:g.64570172G>A, NG_033040.1:g.5542C>T, NG_008929.1:g.13595C>T

Select item 14907877759.

rs1490787775 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:64815685 (GRCh38)
11:64583157 (GRCh37)
Canonical SPDI:: NC_000011.10:64815684:G:A
Validated:: by frequency,by cluster
MAF:: A=0.00159/27 (TOMMO)
HGVS:: NC_000011.10:g.64815685G>A, NC_000011.9:g.64583157G>A, NG_008929.1:g.610C>T

Select item 149072286610.

rs1490722866 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:64801536 (GRCh38)
11:64569008 (GRCh37)
Canonical SPDI:: NC_000011.10:64801535:G:A,NC_000011.10:64801535:G:T
Gene:: MAP4K2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.0001/1 (ALFA)
HGVS:: NC_000011.10:g.64801536G>A, NC_000011.10:g.64801536G>T, NC_000011.9:g.64569008G>A, NC_000011.9:g.64569008G>T, NG_033040.1:g.6706C>T, NG_033040.1:g.6706C>A, NG_008929.1:g.14759C>T, NG_008929.1:g.14759C>A

Select item 149068773211.

rs1490687732 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:64802413 (GRCh38)
11:64569885 (GRCh37)
Canonical SPDI:: NC_000011.10:64802412:C:T
Gene:: MAP4K2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.64802413C>T, NC_000011.9:g.64569885C>T, NG_033040.1:g.5829G>A, NG_008929.1:g.13882G>A

Select item 149059715512.

rs1490597155 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:64815860 (GRCh38)
11:64583332 (GRCh37)
Canonical SPDI:: NC_000011.10:64815859:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.64815860G>A, NC_000011.9:g.64583332G>A, NG_008929.1:g.435C>T

Select item 149055833713.

rs1490558337 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:64802066 (GRCh38)
11:64569538 (GRCh37)
Canonical SPDI:: NC_000011.10:64802065:C:T
Gene:: MAP4K2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.64802066C>T, NC_000011.9:g.64569538C>T, NG_033040.1:g.6176G>A, NM_004579.5:c.366G>A, NM_004579.4:c.366G>A, NM_004579.3:c.366G>A, NM_001307990.2:c.366G>A, NM_001307990.1:c.366G>A, NG_008929.1:g.14229G>A

Select item 149023134214.

rs1490231342 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:64801862 (GRCh38)
11:64569334 (GRCh37)
Canonical SPDI:: NC_000011.10:64801861:C:T
Gene:: MAP4K2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.64801862C>T, NC_000011.9:g.64569334C>T, NG_033040.1:g.6380G>A, NG_008929.1:g.14433G>A

Select item 148975447815.

rs1489754478 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:64810085 (GRCh38)
11:64577557 (GRCh37)
Canonical SPDI:: NC_000011.10:64810084:T:C
Gene:: MEN1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000011.10:g.64810085T>C, NC_000011.9:g.64577557T>C, NG_008929.1:g.6210A>G, NM_000244.4:c.25A>G, NM_000244.3:c.25A>G, NM_130803.3:c.25A>G, NM_130803.2:c.25A>G, NM_130804.3:c.25A>G, NM_130804.2:c.25A>G, NM_130802.3:c.25A>G, NM_130802.2:c.25A>G, NM_130799.3:c.25A>G, NM_130799.2:c.25A>G, NM_130800.3:c.25A>G, NM_130800.2:c.25A>G, NM_130801.3:c.25A>G, NM_130801.2:c.25A>G, NM_001370261.2:c.25A>G, NM_001370261.1:c.25A>G, NM_001370262.2:c.25A>G, NM_001370262.1:c.25A>G, NM_001370251.2:c.25A>G, NM_001370251.1:c.25A>G, NM_001370259.2:c.25A>G, NM_001370259.1:c.25A>G, NM_001370260.2:c.25A>G, NM_001370260.1:c.25A>G, NM_001370263.2:c.25A>G, NM_001370263.1:c.25A>G, NR_176287.1:n.332A>G, NM_001407150.1:c.25A>G, NM_001407143.1:c.25A>G, NM_001407147.1:c.25A>G, NR_176286.1:n.74A>G, NR_176285.1:n.86A>G, NM_001407144.1:c.25A>G, NR_176284.1:n.74A>G, NM_001407142.1:c.25A>G, NM_001407145.1:c.25A>G, NM_001407146.1:c.25A>G, NM_001407151.1:c.25A>G, NM_001407148.1:c.25A>G, NM_001407149.1:c.25A>G, NM_001407152.1:c.25A>G, XM_017017767.3:c.25A>G, XM_017017767.2:c.25A>G, XM_017017767.1:c.25A>G, XM_011545041.3:c.25A>G, XM_017017765.2:c.25A>G, XM_011545040.2:c.25A>G, XM_017017768.2:c.25A>G, XM_017017768.1:c.25A>G, XM_017017766.2:c.25A>G, XM_017017766.1:c.25A>G, NP_000235.3:p.Thr9Ala, NP_570715.2:p.Thr9Ala, NP_570716.2:p.Thr9Ala, NP_570714.2:p.Thr9Ala, NP_570711.2:p.Thr9Ala, NP_570712.2:p.Thr9Ala, NP_570713.2:p.Thr9Ala, NP_001357190.2:p.Thr9Ala, NP_001357191.2:p.Thr9Ala, NP_001357180.2:p.Thr9Ala, NP_001357188.2:p.Thr9Ala, NP_001357189.2:p.Thr9Ala, NP_001357192.2:p.Thr9Ala, XP_016873256.1:p.Thr9Ala, XP_011543343.1:p.Thr9Ala, XP_016873254.1:p.Thr9Ala, XP_011543342.1:p.Thr9Ala, XP_016873257.1:p.Thr9Ala, XP_016873255.1:p.Thr9Ala

Select item 148965622016.

rs1489656220 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:64810871 (GRCh38)
11:64578343 (GRCh37)
Canonical SPDI:: NC_000011.10:64810870:T:C
Gene:: MEN1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,genic_upstream_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000136/19 (GnomAD)
C=0.000223/59 (TOPMED)
HGVS:: NC_000011.10:g.64810871T>C, NC_000011.9:g.64578343T>C, NG_008929.1:g.5424A>G, NM_130803.3:c.-81A>G, NM_130803.2:c.-81A>G, NM_130804.3:c.-81A>G, NM_130804.2:c.-81A>G

Select item 148943674217.

rs1489436742 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:64815279 (GRCh38)
11:64582751 (GRCh37)
Canonical SPDI:: NC_000011.10:64815278:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.64815279T>C, NC_000011.9:g.64582751T>C, NG_008929.1:g.1016A>G

Select item 148926115718.

rs1489261157 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:64810141 (GRCh38)
11:64577613 (GRCh37)
Canonical SPDI:: NC_000011.10:64810140:C:A
Gene:: MEN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: A=0.0001/9 (GnomAD_exomes)
HGVS:: NC_000011.10:g.64810141C>A, NC_000011.9:g.64577613C>A, NG_008929.1:g.6154G>T

Select item 148925143519.

rs1489251435 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 11:64804956 (GRCh38)
11:64572428 (GRCh37)
Canonical SPDI:: NC_000011.10:64804955:T:
Gene:: MEN1 (Varview), MAP4K2 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.64804956del, NC_000011.9:g.64572428del, NG_033040.1:g.3286del, NG_008929.1:g.11339del

Select item 148882843820.

rs1488828438 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:64806817 (GRCh38)
11:64574289 (GRCh37)
Canonical SPDI:: NC_000011.10:64806816:T:C
Gene:: MEN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.64806817T>C, NC_000011.9:g.64574289T>C, NG_033040.1:g.1425A>G, NG_008929.1:g.9478A>G

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