SNP Links for Nucleotide (Select 260593639) - SNP

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Select item 14912855551.

rs1491285555 has merged into rs112696467 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:159716756 (GRCh38)
1:159686546 (GRCh37)
Canonical SPDI:: NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
-=0./0 (PAGE_STUDY)
-=0.38938/1950 (1000Genomes)
HGVS:: NC_000001.11:g.159716756_159716760del, NC_000001.11:g.159716757_159716760del, NC_000001.11:g.159716758_159716760del, NC_000001.11:g.159716759_159716760del, NC_000001.11:g.159716760del, NC_000001.11:g.159716760dup, NC_000001.11:g.159716759_159716760dup, NC_000001.11:g.159716758_159716760dup, NC_000001.11:g.159716757_159716760dup, NC_000001.11:g.159716756_159716760dup, NC_000001.11:g.159716755_159716760dup, NC_000001.11:g.159716754_159716760dup, NC_000001.11:g.159716753_159716760dup, NC_000001.11:g.159716752_159716760dup, NC_000001.11:g.159716751_159716760dup, NC_000001.11:g.159716750_159716760dup, NC_000001.11:g.159716749_159716760dup, NC_000001.11:g.159716748_159716760dup, NC_000001.10:g.159686546_159686550del, NC_000001.10:g.159686547_159686550del, NC_000001.10:g.159686548_159686550del, NC_000001.10:g.159686549_159686550del, NC_000001.10:g.159686550del, NC_000001.10:g.159686550dup, NC_000001.10:g.159686549_159686550dup, NC_000001.10:g.159686548_159686550dup, NC_000001.10:g.159686547_159686550dup, NC_000001.10:g.159686546_159686550dup, NC_000001.10:g.159686545_159686550dup, NC_000001.10:g.159686544_159686550dup, NC_000001.10:g.159686543_159686550dup, NC_000001.10:g.159686542_159686550dup, NC_000001.10:g.159686541_159686550dup, NC_000001.10:g.159686540_159686550dup, NC_000001.10:g.159686539_159686550dup, NC_000001.10:g.159686538_159686550dup, NG_013007.1:g.2841_2845del, NG_013007.1:g.2842_2845del, NG_013007.1:g.2843_2845del, NG_013007.1:g.2844_2845del, NG_013007.1:g.2845del, NG_013007.1:g.2845dup, NG_013007.1:g.2844_2845dup, NG_013007.1:g.2843_2845dup, NG_013007.1:g.2842_2845dup, NG_013007.1:g.2841_2845dup, NG_013007.1:g.2840_2845dup, NG_013007.1:g.2839_2845dup, NG_013007.1:g.2838_2845dup, NG_013007.1:g.2837_2845dup, NG_013007.1:g.2836_2845dup, NG_013007.1:g.2835_2845dup, NG_013007.1:g.2834_2845dup, NG_013007.1:g.2833_2845dup

Select item 14910694612.

rs1491069461 has merged into rs112696467 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:159716756 (GRCh38)
1:159686546 (GRCh37)
Canonical SPDI:: NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:159716744:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
-=0./0 (PAGE_STUDY)
-=0.38938/1950 (1000Genomes)
HGVS:: NC_000001.11:g.159716756_159716760del, NC_000001.11:g.159716757_159716760del, NC_000001.11:g.159716758_159716760del, NC_000001.11:g.159716759_159716760del, NC_000001.11:g.159716760del, NC_000001.11:g.159716760dup, NC_000001.11:g.159716759_159716760dup, NC_000001.11:g.159716758_159716760dup, NC_000001.11:g.159716757_159716760dup, NC_000001.11:g.159716756_159716760dup, NC_000001.11:g.159716755_159716760dup, NC_000001.11:g.159716754_159716760dup, NC_000001.11:g.159716753_159716760dup, NC_000001.11:g.159716752_159716760dup, NC_000001.11:g.159716751_159716760dup, NC_000001.11:g.159716750_159716760dup, NC_000001.11:g.159716749_159716760dup, NC_000001.11:g.159716748_159716760dup, NC_000001.10:g.159686546_159686550del, NC_000001.10:g.159686547_159686550del, NC_000001.10:g.159686548_159686550del, NC_000001.10:g.159686549_159686550del, NC_000001.10:g.159686550del, NC_000001.10:g.159686550dup, NC_000001.10:g.159686549_159686550dup, NC_000001.10:g.159686548_159686550dup, NC_000001.10:g.159686547_159686550dup, NC_000001.10:g.159686546_159686550dup, NC_000001.10:g.159686545_159686550dup, NC_000001.10:g.159686544_159686550dup, NC_000001.10:g.159686543_159686550dup, NC_000001.10:g.159686542_159686550dup, NC_000001.10:g.159686541_159686550dup, NC_000001.10:g.159686540_159686550dup, NC_000001.10:g.159686539_159686550dup, NC_000001.10:g.159686538_159686550dup, NG_013007.1:g.2841_2845del, NG_013007.1:g.2842_2845del, NG_013007.1:g.2843_2845del, NG_013007.1:g.2844_2845del, NG_013007.1:g.2845del, NG_013007.1:g.2845dup, NG_013007.1:g.2844_2845dup, NG_013007.1:g.2843_2845dup, NG_013007.1:g.2842_2845dup, NG_013007.1:g.2841_2845dup, NG_013007.1:g.2840_2845dup, NG_013007.1:g.2839_2845dup, NG_013007.1:g.2838_2845dup, NG_013007.1:g.2837_2845dup, NG_013007.1:g.2836_2845dup, NG_013007.1:g.2835_2845dup, NG_013007.1:g.2834_2845dup, NG_013007.1:g.2833_2845dup

Select item 14910555923.

rs1491055592 has merged into rs59936680 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACACACACACACACACACACAC>-,AC,ACAC,ACACACAC,ACACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACAC [Show Flanks]
Chromosome:: 1:159714275 (GRCh38)
1:159684065 (GRCh37)
Canonical SPDI:: NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000001.11:159714257:CACACACACACACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACACACACAC
Gene:: CRP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACACACACAC=0./0 (ALFA)
CACACACACACACA=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.159714259AC[8], NC_000001.11:g.159714259AC[9], NC_000001.11:g.159714259AC[10], NC_000001.11:g.159714259AC[12], NC_000001.11:g.159714259AC[13], NC_000001.11:g.159714259AC[14], NC_000001.11:g.159714259AC[15], NC_000001.11:g.159714259AC[16], NC_000001.11:g.159714259AC[17], NC_000001.11:g.159714259AC[18], NC_000001.11:g.159714259AC[20], NC_000001.11:g.159714259AC[21], NC_000001.11:g.159714259AC[22], NC_000001.11:g.159714259AC[23], NC_000001.11:g.159714259AC[24], NC_000001.11:g.159714259AC[25], NC_000001.11:g.159714259AC[26], NC_000001.10:g.159684049AC[8], NC_000001.10:g.159684049AC[9], NC_000001.10:g.159684049AC[10], NC_000001.10:g.159684049AC[12], NC_000001.10:g.159684049AC[13], NC_000001.10:g.159684049AC[14], NC_000001.10:g.159684049AC[15], NC_000001.10:g.159684049AC[16], NC_000001.10:g.159684049AC[17], NC_000001.10:g.159684049AC[18], NC_000001.10:g.159684049AC[20], NC_000001.10:g.159684049AC[21], NC_000001.10:g.159684049AC[22], NC_000001.10:g.159684049AC[23], NC_000001.10:g.159684049AC[24], NC_000001.10:g.159684049AC[25], NC_000001.10:g.159684049AC[26], NG_013007.1:g.5295TG[8], NG_013007.1:g.5295TG[9], NG_013007.1:g.5295TG[10], NG_013007.1:g.5295TG[12], NG_013007.1:g.5295TG[13], NG_013007.1:g.5295TG[14], NG_013007.1:g.5295TG[15], NG_013007.1:g.5295TG[16], NG_013007.1:g.5295TG[17], NG_013007.1:g.5295TG[18], NG_013007.1:g.5295TG[20], NG_013007.1:g.5295TG[21], NG_013007.1:g.5295TG[22], NG_013007.1:g.5295TG[23], NG_013007.1:g.5295TG[24], NG_013007.1:g.5295TG[25], NG_013007.1:g.5295TG[26]

Select item 14908634824.

rs1490863482 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:159711957 (GRCh38)
1:159681747 (GRCh37)
Canonical SPDI:: NC_000001.11:159711956:G:A
Gene:: CRP (Varview)
Functional Consequence:: 500B_downstream_variant,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)
A=0.000566/9 (TOMMO)
HGVS:: NC_000001.11:g.159711957G>A, NC_000001.10:g.159681747G>A, NG_013007.1:g.7633C>T

Select item 14905755265.

rs1490575526 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:159717257 (GRCh38)
1:159687047 (GRCh37)
Canonical SPDI:: NC_000001.11:159717256:G: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_000001.11:g.159717257G>C, NC_000001.10:g.159687047G>C, NG_013007.1:g.2333C>G

Select item 14902853446.

rs1490285344 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:159717837 (GRCh38)
1:159687627 (GRCh37)
Canonical SPDI:: NC_000001.11:159717836:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.159717837A>G, NC_000001.10:g.159687627A>G, NG_013007.1:g.1753T>C, NG_076472.1:g.299A>G

Select item 14900859527.

rs1490085952 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:159716865 (GRCh38)
1:159686655 (GRCh37)
Canonical SPDI:: NC_000001.11:159716864:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.159716865C>T, NC_000001.10:g.159686655C>T, NG_013007.1:g.2725G>A

Select item 14897959858.

rs1489795985 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:159717382 (GRCh38)
1:159687172 (GRCh37)
Canonical SPDI:: NC_000001.11:159717381:C:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.159717382C>A, NC_000001.10:g.159687172C>A, NG_013007.1:g.2208G>T

Select item 14892868459.

rs1489286845 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:159716858 (GRCh38)
1:159686648 (GRCh37)
Canonical SPDI:: NC_000001.11:159716857:C:A,NC_000001.11:159716857:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000064/17 (TOPMED)
HGVS:: NC_000001.11:g.159716858C>A, NC_000001.11:g.159716858C>T, NC_000001.10:g.159686648C>A, NC_000001.10:g.159686648C>T, NG_013007.1:g.2732G>T, NG_013007.1:g.2732G>A

Select item 148924702010.

rs1489247020 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:159714413 (GRCh38)
1:159684203 (GRCh37)
Canonical SPDI:: NC_000001.11:159714412:G:A
Gene:: CRP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000001.11:g.159714413G>A, NC_000001.10:g.159684203G>A, NG_013007.1:g.5177C>T

Select item 148913331311.

rs1489133313 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:159715330 (GRCh38)
1:159685120 (GRCh37)
Canonical SPDI:: NC_000001.11:159715329:A:G
Gene:: CRP (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000001.11:g.159715330A>G, NC_000001.10:g.159685120A>G, NG_013007.1:g.4260T>C

Select item 148883786512.

rs1488837865 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:159716501 (GRCh38)
1:159686291 (GRCh37)
Canonical SPDI:: NC_000001.11:159716500:G:A
Gene:: CRP (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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.159716501G>A, NC_000001.10:g.159686291G>A, NG_013007.1:g.3089C>T

Select item 148859449513.

rs1488594495 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:159710350 (GRCh38)
1:159680140 (GRCh37)
Canonical SPDI:: NC_000001.11:159710349:C:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.159710350C>A, NC_000001.10:g.159680140C>A, NG_013007.1:g.9240G>T

Select item 148837665514.

rs1488376655 [Homo sapiens]

Variant type:: DEL
Alleles:: ACT>- [Show Flanks]
Chromosome:: 1:159716109 (GRCh38)
1:159685899 (GRCh37)
Canonical SPDI:: NC_000001.11:159716108:ACT:
Gene:: CRP (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.159716109_159716111del, NC_000001.10:g.159685899_159685901del, NG_013007.1:g.3479_3481del

Select item 148752335815.

rs1487523358 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:159711059 (GRCh38)
1:159680849 (GRCh37)
Canonical SPDI:: NC_000001.11:159711058:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000001.11:g.159711059G>A, NC_000001.10:g.159680849G>A, NG_013007.1:g.8531C>T

Select item 148740721816.

rs1487407218 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:159718349 (GRCh38)
1:159688139 (GRCh37)
Canonical SPDI:: NC_000001.11:159718348:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.159718349C>T, NC_000001.10:g.159688139C>T, NG_013007.1:g.1241G>A

Select item 148717564917.

rs1487175649 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:159714347 (GRCh38)
1:159684137 (GRCh37)
Canonical SPDI:: NC_000001.11:159714346:T:G
Gene:: CRP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000001.11:g.159714347T>G, NC_000001.10:g.159684137T>G, NG_013007.1:g.5243A>C

Select item 148710206718.

rs1487102067 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 1:159711668 (GRCh38)
1:159681458 (GRCh37)
Canonical SPDI:: NC_000001.11:159711667:C:
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000071/1 (ALFA)
-=0.000019/5 (TOPMED)
-=0.000029/4 (GnomAD)
HGVS:: NC_000001.11:g.159711668del, NC_000001.10:g.159681458del, NG_013007.1:g.7922del

Select item 148687438919.

rs1486874389 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 1:159715471 (GRCh38)
1:159685261 (GRCh37)
Canonical SPDI:: NC_000001.11:159715470:TTTTT:TTTT
Gene:: CRP (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: TTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.159715475del, NC_000001.10:g.159685265del, NG_013007.1:g.4119del

Select item 148640826620.

rs1486408266 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:159715145 (GRCh38)
1:159684935 (GRCh37)
Canonical SPDI:: NC_000001.11:159715144:C:T
Gene:: CRP (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.159715145C>T, NC_000001.10:g.159684935C>T, NG_013007.1:g.4445G>A

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