SNP Links for Gene (Select 10962) - SNP

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Links from Gene

Items: 1 to 20 of 1000

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Select item 14909168301.

rs1490916830 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:151062357 (GRCh38)
1:151034833 (GRCh37)
Canonical SPDI:: NC_000001.11:151062356:T:A
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
A=0.000022/3 (GnomAD)
HGVS:: NC_000001.11:g.151062357T>A, NC_000001.10:g.151034833T>A

Select item 14909132772.

rs1490913277 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:151062689 (GRCh38)
1:151035165 (GRCh37)
Canonical SPDI:: NC_000001.11:151062688:A:C
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.151062689A>C, NC_000001.10:g.151035165A>C

Select item 14904074543.

rs1490407454 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:151062731 (GRCh38)
1:151035207 (GRCh37)
Canonical SPDI:: NC_000001.11:151062730:G:T
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.151062731G>T, NC_000001.10:g.151035207G>T

Select item 14897627874.

rs1489762787 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:151067173 (GRCh38)
1:151039649 (GRCh37)
Canonical SPDI:: NC_000001.11:151067172:A:G
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000001.11:g.151067173A>G, NC_000001.10:g.151039649A>G

Select item 14895160515.

rs1489516051 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:151063403 (GRCh38)
1:151035879 (GRCh37)
Canonical SPDI:: NC_000001.11:151063402:C:A
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.151063403C>A, NC_000001.10:g.151035879C>A

Select item 14890614876.

rs1489061487 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:151063616 (GRCh38)
1:151036092 (GRCh37)
Canonical SPDI:: NC_000001.11:151063615:G:A
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000156/1 (1000Genomes)
A=0.000684/2 (KOREAN)
HGVS:: NC_000001.11:g.151063616G>A, NC_000001.10:g.151036092G>A

Select item 14889877387.

rs1488987738 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:151064605 (GRCh38)
1:151037081 (GRCh37)
Canonical SPDI:: NC_000001.11:151064604:A:T
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.151064605A>T, NC_000001.10:g.151037081A>T

Select item 14887541208.

rs1488754120 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:151064504 (GRCh38)
1:151036980 (GRCh37)
Canonical SPDI:: NC_000001.11:151064503:A:G
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000001.11:g.151064504A>G, NC_000001.10:g.151036980A>G

Select item 14887257959.

rs1488725795 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:151065749 (GRCh38)
1:151038225 (GRCh37)
Canonical SPDI:: NC_000001.11:151065748:C:T
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.151065749C>T, NC_000001.10:g.151038225C>T

Select item 148807685010.

rs1488076850 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:151061149 (GRCh38)
1:151033625 (GRCh37)
Canonical SPDI:: NC_000001.11:151061148:G:C
Gene:: MLLT11 (Varview), CDC42SE1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000019/5 (TOPMED)
HGVS:: NC_000001.11:g.151061149G>C, NC_000001.10:g.151033625G>C

Select item 148807293111.

rs1488072931 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 1:151064008 (GRCh38)
1:151036485 (GRCh37)
Canonical SPDI:: NC_000001.11:151064008:TTT:TTTT
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTT=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.151064011dup, NC_000001.10:g.151036487dup

Select item 148804106912.

rs1488041069 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:151065063 (GRCh38)
1:151037539 (GRCh37)
Canonical SPDI:: NC_000001.11:151065062:G:A
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.151065063G>A, NC_000001.10:g.151037539G>A

Select item 148751754113.

rs1487517541 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:151065199 (GRCh38)
1:151037675 (GRCh37)
Canonical SPDI:: NC_000001.11:151065198:A:C
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.151065199A>C, NC_000001.10:g.151037675A>C

Select item 148726107814.

rs1487261078 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:151068340 (GRCh38)
1:151040816 (GRCh37)
Canonical SPDI:: NC_000001.11:151068339:A:G
Gene:: MLLT11 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.151068340A>G, NC_000001.10:g.151040816A>G, NM_006818.4:c.*843A>G, NM_006818.3:c.*843A>G

Select item 148706070215.

rs1487060702 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:151065585 (GRCh38)
1:151038061 (GRCh37)
Canonical SPDI:: NC_000001.11:151065584:G:T
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.151065585G>T, NC_000001.10:g.151038061G>T

Select item 148704578816.

rs1487045788 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:151065570 (GRCh38)
1:151038046 (GRCh37)
Canonical SPDI:: NC_000001.11:151065569:C:T
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.151065570C>T, NC_000001.10:g.151038046C>T

Select item 148698460017.

rs1486984600 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:151066781 (GRCh38)
1:151039257 (GRCh37)
Canonical SPDI:: NC_000001.11:151066780:C:G,NC_000001.11:151066780:C:T
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
G=0.000177/3 (TOMMO)
HGVS:: NC_000001.11:g.151066781C>G, NC_000001.11:g.151066781C>T, NC_000001.10:g.151039257C>G, NC_000001.10:g.151039257C>T

Select item 148697714418.

rs1486977144 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:151057963 (GRCh38)
1:151030439 (GRCh37)
Canonical SPDI:: NC_000001.11:151057962:G:A
Gene:: CDC42SE1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.151057963G>A, NC_000001.10:g.151030439G>A

Select item 148636885319.

rs1486368853 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:151057981 (GRCh38)
1:151030457 (GRCh37)
Canonical SPDI:: NC_000001.11:151057980:G:A
Gene:: CDC42SE1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.151057981G>A, NC_000001.10:g.151030457G>A

Select item 148631259320.

rs1486312593 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:151062458 (GRCh38)
1:151034934 (GRCh37)
Canonical SPDI:: NC_000001.11:151062457:G:A
Gene:: MLLT11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.151062458G>A, NC_000001.10:g.151034934G>A

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