SNP Links for Gene (Select 8536) - SNP

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Select item 14913964721.

rs1491396472 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 3:9763423 (GRCh38)
3:9805107 (GRCh37)
Canonical SPDI:: NC_000003.12:9763421:ACA:A
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000043/6 (GnomAD)
-=0.000312/2 (1000Genomes)
HGVS:: NC_000003.12:g.9763423_9763424del, NC_000003.11:g.9805107_9805108del, NG_012106.1:g.18480_18481del

Select item 14912866112.

rs1491286611 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 3:9763422 (GRCh38)
3:9805107 (GRCh37)
Canonical SPDI:: NC_000003.12:9763422:C:CC
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.9763423dup, NC_000003.11:g.9805107dup, NG_012106.1:g.18480dup

Select item 14910053543.

rs1491005354 has merged into rs571944870 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA [Show Flanks]
Chromosome:: 3:9763419 (GRCh38)
3:9805103 (GRCh37)
Canonical SPDI:: NC_000003.12:9763403:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:9763403:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:9763403:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:9763403:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:9763403:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:9763403:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000003.12:9763403:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:9763403:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:9763403:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAA=0./0 (ALFA)
A=0.01375/8 (NorthernSweden)
HGVS:: NC_000003.12:g.9763419_9763422del, NC_000003.12:g.9763420_9763422del, NC_000003.12:g.9763421_9763422del, NC_000003.12:g.9763422del, NC_000003.12:g.9763422dup, NC_000003.12:g.9763421_9763422dup, NC_000003.12:g.9763420_9763422dup, NC_000003.12:g.9763419_9763422dup, NC_000003.12:g.9763417_9763422dup, NC_000003.11:g.9805103_9805106del, NC_000003.11:g.9805104_9805106del, NC_000003.11:g.9805105_9805106del, NC_000003.11:g.9805106del, NC_000003.11:g.9805106dup, NC_000003.11:g.9805105_9805106dup, NC_000003.11:g.9805104_9805106dup, NC_000003.11:g.9805103_9805106dup, NC_000003.11:g.9805101_9805106dup, NG_012106.1:g.18476_18479del, NG_012106.1:g.18477_18479del, NG_012106.1:g.18478_18479del, NG_012106.1:g.18479del, NG_012106.1:g.18479dup, NG_012106.1:g.18478_18479dup, NG_012106.1:g.18477_18479dup, NG_012106.1:g.18476_18479dup, NG_012106.1:g.18474_18479dup

Select item 14909806104.

rs1490980610 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 3:9758464 (GRCh38)
3:9800148 (GRCh37)
Canonical SPDI:: NC_000003.12:9758463:C:G
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_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_000003.12:g.9758464C>G, NC_000003.11:g.9800148C>G, NG_012106.1:g.13521C>G

Select item 14908468185.

rs1490846818 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:9759467 (GRCh38)
3:9801151 (GRCh37)
Canonical SPDI:: NC_000003.12:9759466:G:A
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: downstream_transcript_variant,intron_variant,genic_downstream_transcript_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_000003.12:g.9759467G>A, NC_000003.11:g.9801151G>A, NG_012106.1:g.14524G>A

Select item 14905615766.

rs1490561576 has merged into rs55972033 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:9764640 (GRCh38)
3:9806324 (GRCh37)
Canonical SPDI:: NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:9764628:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000003.12:g.9764640_9764645del, NC_000003.12:g.9764641_9764645del, NC_000003.12:g.9764643_9764645del, NC_000003.12:g.9764644_9764645del, NC_000003.12:g.9764645del, NC_000003.12:g.9764645dup, NC_000003.12:g.9764644_9764645dup, NC_000003.12:g.9764642_9764645dup, NC_000003.12:g.9764638_9764645dup, NC_000003.12:g.9764637_9764645dup, NC_000003.12:g.9764636_9764645dup, NC_000003.12:g.9764635_9764645dup, NC_000003.12:g.9764634_9764645dup, NC_000003.12:g.9764632_9764645dup, NC_000003.12:g.9764631_9764645dup, NC_000003.12:g.9764630_9764645dup, NC_000003.12:g.9764629_9764645dup, NC_000003.12:g.9764645_9764646insTTTTTTTTTTTTTTTTTT, NC_000003.11:g.9806324_9806329del, NC_000003.11:g.9806325_9806329del, NC_000003.11:g.9806327_9806329del, NC_000003.11:g.9806328_9806329del, NC_000003.11:g.9806329del, NC_000003.11:g.9806329dup, NC_000003.11:g.9806328_9806329dup, NC_000003.11:g.9806326_9806329dup, NC_000003.11:g.9806322_9806329dup, NC_000003.11:g.9806321_9806329dup, NC_000003.11:g.9806320_9806329dup, NC_000003.11:g.9806319_9806329dup, NC_000003.11:g.9806318_9806329dup, NC_000003.11:g.9806316_9806329dup, NC_000003.11:g.9806315_9806329dup, NC_000003.11:g.9806314_9806329dup, NC_000003.11:g.9806313_9806329dup, NC_000003.11:g.9806329_9806330insTTTTTTTTTTTTTTTTTT, NG_012106.1:g.19697_19702del, NG_012106.1:g.19698_19702del, NG_012106.1:g.19700_19702del, NG_012106.1:g.19701_19702del, NG_012106.1:g.19702del, NG_012106.1:g.19702dup, NG_012106.1:g.19701_19702dup, NG_012106.1:g.19699_19702dup, NG_012106.1:g.19695_19702dup, NG_012106.1:g.19694_19702dup, NG_012106.1:g.19693_19702dup, NG_012106.1:g.19692_19702dup, NG_012106.1:g.19691_19702dup, NG_012106.1:g.19689_19702dup, NG_012106.1:g.19688_19702dup, NG_012106.1:g.19687_19702dup, NG_012106.1:g.19686_19702dup, NG_012106.1:g.19702_19703insTTTTTTTTTTTTTTTTTT

Select item 14901686627.

rs1490168662 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:9758803 (GRCh38)
3:9800487 (GRCh37)
Canonical SPDI:: NC_000003.12:9758802:T:C
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_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_000003.12:g.9758803T>C, NC_000003.11:g.9800487T>C, NG_012106.1:g.13860T>C

Select item 14899829298.

rs1489982929 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 3:9767274 (GRCh38)
3:9808958 (GRCh37)
Canonical SPDI:: NC_000003.12:9767273:C:G
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000003.12:g.9767274C>G, NC_000003.11:g.9808958C>G, NG_012106.1:g.22331C>G

Select item 14898165649.

rs1489816564 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 3:9767079 (GRCh38)
3:9808763 (GRCh37)
Canonical SPDI:: NC_000003.12:9767078:C:G,NC_000003.12:9767078:C:T
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: downstream_transcript_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000003.12:g.9767079C>G, NC_000003.12:g.9767079C>T, NC_000003.11:g.9808763C>G, NC_000003.11:g.9808763C>T, NG_012106.1:g.22136C>G, NG_012106.1:g.22136C>T

Select item 148975377510.

rs1489753775 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:9771643 (GRCh38)
3:9813327 (GRCh37)
Canonical SPDI:: NC_000003.12:9771642:T:C
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_downstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000021/3 (GnomAD)
C=0.000026/7 (TOPMED)
HGVS:: NC_000003.12:g.9771643T>C, NC_000003.11:g.9813327T>C

Select item 148962078511.

rs1489620785 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:9761480 (GRCh38)
3:9803164 (GRCh37)
Canonical SPDI:: NC_000003.12:9761479:C:T
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.9761480C>T, NC_000003.11:g.9803164C>T, NG_012106.1:g.16537C>T, NM_003656.5:c.613G>A, NM_003656.4:c.613G>A, XM_005265517.4:c.481G>A, XM_005265517.3:c.481G>A, XM_005265517.2:c.481G>A, XM_005265517.1:c.481G>A, XM_005265516.3:c.613G>A, XM_005265516.2:c.613G>A, XM_005265516.1:c.613G>A, XM_017007354.2:c.481G>A, XM_017007354.1:c.481G>A, XM_047449089.1:c.613G>A, NP_003647.1:p.Gly205Ser, XP_005265574.1:p.Gly161Ser, XP_005265573.1:p.Gly205Ser, XP_016862843.1:p.Gly161Ser, XP_047305045.1:p.Gly205Ser

Select item 148956998912.

rs1489569989 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:9760555 (GRCh38)
3:9802239 (GRCh37)
Canonical SPDI:: NC_000003.12:9760554:G:A
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_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_000003.12:g.9760555G>A, NC_000003.11:g.9802239G>A, NG_012106.1:g.15612G>A

Select item 148952284913.

rs1489522849 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 3:9768263 (GRCh38)
3:9809947 (GRCh37)
Canonical SPDI:: NC_000003.12:9768262:G:A,NC_000003.12:9768262:G:C
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000003.12:g.9768263G>A, NC_000003.12:g.9768263G>C, NC_000003.11:g.9809947G>A, NC_000003.11:g.9809947G>C, NG_012106.1:g.23320G>A, NG_012106.1:g.23320G>C

Select item 148946550614.

rs1489465506 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:9767250 (GRCh38)
3:9808934 (GRCh37)
Canonical SPDI:: NC_000003.12:9767249:A:C
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_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_000003.12:g.9767250A>C, NC_000003.11:g.9808934A>C, NG_012106.1:g.22307A>C

Select item 148943495015.

rs1489434950 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:9767871 (GRCh38)
3:9809555 (GRCh37)
Canonical SPDI:: NC_000003.12:9767870:A:G
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_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_000003.12:g.9767871A>G, NC_000003.11:g.9809555A>G, NG_012106.1:g.22928A>G

Select item 148863064316.

rs1488630643 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GCCAAGCAGAAGGAAGTA [Show Flanks]
Chromosome:: 3:9760472 (GRCh38)
3:9802157 (GRCh37)
Canonical SPDI:: NC_000003.12:9760472:AGCCAAGCAGAAGGAAGTA:AGCCAAGCAGAAGGAAGTAGCCAAGCAGAAGGAAGTA
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: AGCCAAGCAGAAGGAAGTAGCCAAGCAGAAGGAAGTA=0./0 (ALFA)
AGCCAAGCAGAAGGAAGT=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.9760474_9760491dup, NC_000003.11:g.9802158_9802175dup, NG_012106.1:g.15531_15548dup

Select item 148862549517.

rs1488625495 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:9758754 (GRCh38)
3:9800438 (GRCh37)
Canonical SPDI:: NC_000003.12:9758753:C:T
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000054/1 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000003.12:g.9758754C>T, NC_000003.11:g.9800438C>T, NG_012106.1:g.13811C>T

Select item 148854294418.

rs1488542944 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 3:9767750 (GRCh38)
3:9809434 (GRCh37)
Canonical SPDI:: NC_000003.12:9767749:G:C,NC_000003.12:9767749:G:T
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,5_prime_UTR_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_000003.12:g.9767750G>C, NC_000003.12:g.9767750G>T, NC_000003.11:g.9809434G>C, NC_000003.11:g.9809434G>T, NG_012106.1:g.22807G>C, NG_012106.1:g.22807G>T, NM_003656.5:c.-1C>G, NM_003656.5:c.-1C>A, NM_003656.4:c.-1C>G, NM_003656.4:c.-1C>A, XM_005265517.4:c.-1C>G, XM_005265517.4:c.-1C>A, XM_005265517.3:c.-1C>G, XM_005265517.3:c.-1C>A, XM_005265517.2:c.-1C>G, XM_005265517.2:c.-1C>A, XM_005265517.1:c.-1C>G, XM_005265517.1:c.-1C>A, XM_005265516.3:c.-1C>G, XM_005265516.3:c.-1C>A, XM_005265516.2:c.-1C>G, XM_005265516.2:c.-1C>A, XM_005265516.1:c.-1C>G, XM_005265516.1:c.-1C>A, XM_017007354.2:c.-1C>G, XM_017007354.2:c.-1C>A, XM_017007354.1:c.-1C>G, XM_017007354.1:c.-1C>A, XM_047449089.1:c.-1C>G, XM_047449089.1:c.-1C>A

Select item 148825654619.

rs1488256546 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:9765409 (GRCh38)
3:9807093 (GRCh37)
Canonical SPDI:: NC_000003.12:9765408:T:C
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000003.12:g.9765409T>C, NC_000003.11:g.9807093T>C, NG_012106.1:g.20466T>C

Select item 148820773220.

rs1488207732 has merged into rs202012854 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:9764625 (GRCh38)
3:9806309 (GRCh37)
Canonical SPDI:: NC_000003.12:9764617:TTTTTTTTTT:TTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:9764617:TTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: OGG1 (Varview), CAMK1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
TTTTTT=0.0035/2 (NorthernSweden)
HGVS:: NC_000003.12:g.9764625_9764627del, NC_000003.12:g.9764626_9764627del, NC_000003.12:g.9764627del, NC_000003.12:g.9764627dup, NC_000003.12:g.9764626_9764627dup, NC_000003.12:g.9764625_9764627dup, NC_000003.12:g.9764624_9764627dup, NC_000003.12:g.9764623_9764627dup, NC_000003.12:g.9764622_9764627dup, NC_000003.12:g.9764621_9764627dup, NC_000003.12:g.9764620_9764627dup, NC_000003.12:g.9764619_9764627dup, NC_000003.12:g.9764627_9764628insTTTTTTTTTTT, NC_000003.12:g.9764627_9764628insTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.9806309_9806311del, NC_000003.11:g.9806310_9806311del, NC_000003.11:g.9806311del, NC_000003.11:g.9806311dup, NC_000003.11:g.9806310_9806311dup, NC_000003.11:g.9806309_9806311dup, NC_000003.11:g.9806308_9806311dup, NC_000003.11:g.9806307_9806311dup, NC_000003.11:g.9806306_9806311dup, NC_000003.11:g.9806305_9806311dup, NC_000003.11:g.9806304_9806311dup, NC_000003.11:g.9806303_9806311dup, NC_000003.11:g.9806311_9806312insTTTTTTTTTTT, NC_000003.11:g.9806311_9806312insTTTTTTTTTTTTTTTTTTTTTTT, NG_012106.1:g.19682_19684del, NG_012106.1:g.19683_19684del, NG_012106.1:g.19684del, NG_012106.1:g.19684dup, NG_012106.1:g.19683_19684dup, NG_012106.1:g.19682_19684dup, NG_012106.1:g.19681_19684dup, NG_012106.1:g.19680_19684dup, NG_012106.1:g.19679_19684dup, NG_012106.1:g.19678_19684dup, NG_012106.1:g.19677_19684dup, NG_012106.1:g.19676_19684dup, NG_012106.1:g.19684_19685insTTTTTTTTTTT, NG_012106.1:g.19684_19685insTTTTTTTTTTTTTTTTTTTTTTT

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