SNP Links for Nucleotide (Select 392973718) - SNP

Links from Nucleotide

Items: 1 to 20 of 134

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Select item 14902417911.

rs1490241791 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 9:69306855 (GRCh38)
9:71921771 (GRCh37)
Canonical SPDI:: NC_000009.12:69306854:C:A,NC_000009.12:69306854:C:G
Gene:: BANCR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.69306855C>A, NC_000009.12:g.69306855C>G, NC_000009.11:g.71921771C>A, NC_000009.11:g.71921771C>G, NR_047671.2:n.202G>T, NR_047671.2:n.202G>C

Select item 14899266042.

rs1489926604 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:69296840 (GRCh38)
9:71911756 (GRCh37)
Canonical SPDI:: NC_000009.12:69296839:T:C
Gene:: BANCR (Varview), LOC124902176 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.69296840T>C, NC_000009.11:g.71911756T>C, NR_047671.2:n.516A>G, XR_007061567.1:n.215T>C

Select item 14873274743.

rs1487327474 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:69307020 (GRCh38)
9:71921936 (GRCh37)
Canonical SPDI:: NC_000009.12:69307019:T:C
Gene:: BANCR (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_000009.12:g.69307020T>C, NC_000009.11:g.71921936T>C, NR_047671.2:n.37A>G

Select item 14835186994.

rs1483518699 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:69296783 (GRCh38)
9:71911699 (GRCh37)
Canonical SPDI:: NC_000009.12:69296782:G:T
Gene:: BANCR (Varview), LOC124902176 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000142/2 (ALFA)
T=0.000043/6 (GnomAD)
T=0.00006/16 (TOPMED)
HGVS:: NC_000009.12:g.69296783G>T, NC_000009.11:g.71911699G>T, NR_047671.2:n.573C>A, XR_007061567.1:n.158G>T

Select item 14802933335.

rs1480293333 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:69306929 (GRCh38)
9:71921845 (GRCh37)
Canonical SPDI:: NC_000009.12:69306928:A:C
Gene:: BANCR (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=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.69306929A>C, NC_000009.11:g.71921845A>C, NR_047671.2:n.128T>G

Select item 14657640436.

rs1465764043 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:69296764 (GRCh38)
9:71911680 (GRCh37)
Canonical SPDI:: NC_000009.12:69296763:T:C
Gene:: BANCR (Varview), LOC124902176 (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_000009.12:g.69296764T>C, NC_000009.11:g.71911680T>C, NR_047671.2:n.592A>G, XR_007061567.1:n.139T>C

Select item 14632216617.

rs1463221661 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 9:69306901 (GRCh38)
9:71921817 (GRCh37)
Canonical SPDI:: NC_000009.12:69306900:G:A,NC_000009.12:69306900:G:T
Gene:: BANCR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.69306901G>A, NC_000009.12:g.69306901G>T, NC_000009.11:g.71921817G>A, NC_000009.11:g.71921817G>T, NR_047671.2:n.156C>T, NR_047671.2:n.156C>A

Select item 14598126088.

rs1459812608 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:69306197 (GRCh38)
9:71921113 (GRCh37)
Canonical SPDI:: NC_000009.12:69306196:A:G
Gene:: BANCR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.69306197A>G, NC_000009.11:g.71921113A>G, NR_047671.2:n.297T>C

Select item 14536833469.

rs1453683346 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:69296829 (GRCh38)
9:71911745 (GRCh37)
Canonical SPDI:: NC_000009.12:69296828:A:C
Gene:: BANCR (Varview), LOC124902176 (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_000009.12:g.69296829A>C, NC_000009.11:g.71911745A>C, NR_047671.2:n.527T>G, XR_007061567.1:n.204A>C

Select item 145149797710.

rs1451497977 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:69306161 (GRCh38)
9:71921077 (GRCh37)
Canonical SPDI:: NC_000009.12:69306160:G:C
Gene:: BANCR (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_000009.12:g.69306161G>C, NC_000009.11:g.71921077G>C, NR_047671.2:n.333C>G

Select item 144911794711.

rs1449117947 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 9:69305048 (GRCh38)
9:71919964 (GRCh37)
Canonical SPDI:: NC_000009.12:69305047:TT:T
Gene:: BANCR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.69305049del, NC_000009.11:g.71919965del, NR_047671.2:n.376del

Select item 144750377812.

rs1447503778 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:69306243 (GRCh38)
9:71921159 (GRCh37)
Canonical SPDI:: NC_000009.12:69306242:C:T
Gene:: BANCR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.69306243C>T, NC_000009.11:g.71921159C>T, NR_047671.2:n.251G>A

Select item 144302477913.

rs1443024779 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 9:69306223 (GRCh38)
9:71921139 (GRCh37)
Canonical SPDI:: NC_000009.12:69306222:CCC:CC
Gene:: BANCR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000019/5 (TOPMED)
HGVS:: NC_000009.12:g.69306225del, NC_000009.11:g.71921141del, NR_047671.2:n.271del

Select item 143759951914.

rs1437599519 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:69306218 (GRCh38)
9:71921134 (GRCh37)
Canonical SPDI:: NC_000009.12:69306217:A:T
Gene:: BANCR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000009.12:g.69306218A>T, NC_000009.11:g.71921134A>T, NR_047671.2:n.276T>A

Select item 143214847515.

rs1432148475 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:69306924 (GRCh38)
9:71921840 (GRCh37)
Canonical SPDI:: NC_000009.12:69306923:T:C
Gene:: BANCR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.69306924T>C, NC_000009.11:g.71921840T>C, NR_047671.2:n.133A>G

Select item 143136537816.

rs1431365378 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 9:69296800 (GRCh38)
9:71911716 (GRCh37)
Canonical SPDI:: NC_000009.12:69296799:C:
Gene:: BANCR (Varview), LOC124902176 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.69296800del, NC_000009.11:g.71911716del, NR_047671.2:n.556del, XR_007061567.1:n.175del

Select item 142847015017.

rs1428470150 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:69296811 (GRCh38)
9:71911727 (GRCh37)
Canonical SPDI:: NC_000009.12:69296810:G:A
Gene:: BANCR (Varview), LOC124902176 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.69296811G>A, NC_000009.11:g.71911727G>A, NR_047671.2:n.545C>T, XR_007061567.1:n.186G>A

Select item 140770365018.

rs1407703650 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:69307009 (GRCh38)
9:71921925 (GRCh37)
Canonical SPDI:: NC_000009.12:69307008:A:G
Gene:: BANCR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.69307009A>G, NC_000009.11:g.71921925A>G, NR_047671.2:n.48T>C

Select item 139222323319.

rs1392223233 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:69304997 (GRCh38)
9:71919913 (GRCh37)
Canonical SPDI:: NC_000009.12:69304996:G:A,NC_000009.12:69304996:G:C
Gene:: BANCR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.69304997G>A, NC_000009.12:g.69304997G>C, NC_000009.11:g.71919913G>A, NC_000009.11:g.71919913G>C, NR_047671.2:n.427C>T, NR_047671.2:n.427C>G

Select item 139217081120.

rs1392170811 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:69304964 (GRCh38)
9:71919880 (GRCh37)
Canonical SPDI:: NC_000009.12:69304963:C:T
Gene:: BANCR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.69304964C>T, NC_000009.11:g.71919880C>T, NR_047671.2:n.460G>A

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