SNP Links for Nucleotide (Select 223468639) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Nucleotide

Items: 1 to 20 of 1782

<< First< Prev

Page of 90

Next >Last >>

Select item 14914240971.

rs1491424097 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CT [Show Flanks]
Chromosome:: 10:26647016 (GRCh38)
10:26935946 (GRCh37)
Canonical SPDI:: NC_000010.11:26647016:T:TCT
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCT=0.00061/10 (ALFA)
TC=0.00432/122 (TOMMO)
HGVS:: NC_000010.11:g.26647017_26647018insCT, NC_000010.10:g.26935946_26935947insCT, NR_026794.1:n.3910_3911insCT

Select item 14913160502.

rs1491316050 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 10:26647016 (GRCh38)
10:26935945 (GRCh37)
Canonical SPDI:: NC_000010.11:26647015:TT:
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.26647016_26647017del, NC_000010.10:g.26935945_26935946del, NR_026794.1:n.3909_3910del

Select item 14909571443.

rs1490957144 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:26647609 (GRCh38)
10:26936538 (GRCh37)
Canonical SPDI:: NC_000010.11:26647608:C:T
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.01232/55 (ALFA)
T=0.01794/507 (TOMMO)
T=0.02669/78 (KOREAN)
HGVS:: NC_000010.11:g.26647609C>T, NC_000010.10:g.26936538C>T, NR_026794.1:n.4502C>T

Select item 14901248824.

rs1490124882 [Homo sapiens]

Variant type:: DEL
Alleles:: GGC>- [Show Flanks]
Chromosome:: 10:26646173 (GRCh38)
10:26935102 (GRCh37)
Canonical SPDI:: NC_000010.11:26646172:GGC:
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000010.11:g.26646173_26646175del, NC_000010.10:g.26935102_26935104del, NR_026794.1:n.3066_3068del

Select item 14901144775.

rs1490114477 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:26645052 (GRCh38)
10:26933981 (GRCh37)
Canonical SPDI:: NC_000010.11:26645051:T:C
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.26645052T>C, NC_000010.10:g.26933981T>C, NR_026794.1:n.1945T>C

Select item 14899601006.

rs1489960100 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAG>- [Show Flanks]
Chromosome:: 10:26646691 (GRCh38)
10:26935620 (GRCh37)
Canonical SPDI:: NC_000010.11:26646688:AGAAG:AG
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AG=0./0 (ALFA)
-=0.00071/12 (TOMMO)
HGVS:: NC_000010.11:g.26646691_26646693del, NC_000010.10:g.26935620_26935622del, NR_026794.1:n.3584_3586del

Select item 14890216977.

rs1489021697 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTT>- [Show Flanks]
Chromosome:: 10:26643844 (GRCh38)
10:26932773 (GRCh37)
Canonical SPDI:: NC_000010.11:26643836:TCTTCTTCTT:TCTTCTT
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTTCTT=0./0 (ALFA)
-=0.000014/2 (GnomAD)
-=0.000019/5 (TOPMED)
-=0.000312/2 (1000Genomes)
HGVS:: NC_000010.11:g.26643838CTT[2], NC_000010.10:g.26932767CTT[2], NR_026794.1:n.731CTT[2]

Select item 14883847368.

rs1488384736 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:26649541 (GRCh38)
10:26938470 (GRCh37)
Canonical SPDI:: NC_000010.11:26649540:C:G
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.26649541C>G, NC_000010.10:g.26938470C>G, NR_026794.1:n.5424C>G

Select item 14882743019.

rs1488274301 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:26643924 (GRCh38)
10:26932853 (GRCh37)
Canonical SPDI:: NC_000010.11:26643923:G:A
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.26643924G>A, NC_000010.10:g.26932853G>A, NR_026794.1:n.817G>A

Select item 148824307710.

rs1488243077 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:26644679 (GRCh38)
10:26933608 (GRCh37)
Canonical SPDI:: NC_000010.11:26644678:T:C
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000010.11:g.26644679T>C, NC_000010.10:g.26933608T>C, NR_026794.1:n.1572T>C

Select item 148819246611.

rs1488192466 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:26649001 (GRCh38)
10:26937930 (GRCh37)
Canonical SPDI:: NC_000010.11:26649000:G:A
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.26649001G>A, NC_000010.10:g.26937930G>A, NR_026794.1:n.5226G>A

Select item 148725787212.

rs1487257872 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:26645154 (GRCh38)
10:26934083 (GRCh37)
Canonical SPDI:: NC_000010.11:26645153:T:C
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_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_000010.11:g.26645154T>C, NC_000010.10:g.26934083T>C, NR_026794.1:n.2047T>C

Select item 148698295813.

rs1486982958 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:26650630 (GRCh38)
10:26939559 (GRCh37)
Canonical SPDI:: NC_000010.11:26650629:G:A
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.26650630G>A, NC_000010.10:g.26939559G>A, NR_026794.1:n.5553G>A

Select item 148680106314.

rs1486801063 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:26644310 (GRCh38)
10:26933239 (GRCh37)
Canonical SPDI:: NC_000010.11:26644309:A:G
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.26644310A>G, NC_000010.10:g.26933239A>G, NR_026794.1:n.1203A>G

Select item 148671494415.

rs1486714944 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:26648193 (GRCh38)
10:26937122 (GRCh37)
Canonical SPDI:: NC_000010.11:26648192:A:C
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_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_000010.11:g.26648193A>C, NC_000010.10:g.26937122A>C, NR_026794.1:n.5086A>C

Select item 148664349316.

rs1486643493 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:26647078 (GRCh38)
10:26936007 (GRCh37)
Canonical SPDI:: NC_000010.11:26647077:T:C
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000024/3 (GnomAD)
C=0.000026/7 (TOPMED)
HGVS:: NC_000010.11:g.26647078T>C, NC_000010.10:g.26936007T>C, NR_026794.1:n.3971T>C

Select item 148647377517.

rs1486473775 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:26644061 (GRCh38)
10:26932990 (GRCh37)
Canonical SPDI:: NC_000010.11:26644060:G:A
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.006337/96 (ALFA)
A=0.000205/26 (GnomAD)
A=0.004247/120 (TOMMO)
A=0.008432/54 (1000Genomes)
A=0.111567/326 (KOREAN)
HGVS:: NC_000010.11:g.26644061G>A, NC_000010.10:g.26932990G>A, NR_026794.1:n.954G>A

Select item 148615615018.

rs1486156150 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:26644535 (GRCh38)
10:26933464 (GRCh37)
Canonical SPDI:: NC_000010.11:26644534:C:T
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.26644535C>T, NC_000010.10:g.26933464C>T, NR_026794.1:n.1428C>T

Select item 148523238519.

rs1485232385 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:26645586 (GRCh38)
10:26934515 (GRCh37)
Canonical SPDI:: NC_000010.11:26645585:G:A
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000010.11:g.26645586G>A, NC_000010.10:g.26934515G>A, NR_026794.1:n.2479G>A

Select item 148505525420.

rs1485055254 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:26648197 (GRCh38)
10:26937126 (GRCh37)
Canonical SPDI:: NC_000010.11:26648196:C:T
Gene:: FAM238B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000010.11:g.26648197C>T, NC_000010.10:g.26937126C>T, NR_026794.1:n.5090C>T