SNP Links for Nucleotide (Select 197100415) - SNP

Links from Nucleotide

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Select item 14915823281.

rs1491582328 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 19:40848940 (GRCh38)
19:41354845 (GRCh37)
Canonical SPDI:: NC_000019.10:40848939:TA:
Gene:: CYP2A6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00051/6 (ALFA)
-=0.00002/1 (GnomAD)
HGVS:: NC_000019.10:g.40848940_40848941del, NC_000019.9:g.41354845_41354846del, NG_008377.1:g.6507_6508del

Select item 14915116822.

rs1491511682 [Homo sapiens]

Variant type:: INS
Alleles:: ->G,GAG,GAGAG,GAGAGAG,GAGAGG,GAGG,GG,GGG [Show Flanks]
Chromosome:: 19:40848977 (GRCh38)
19:41354883 (GRCh37)
Canonical SPDI:: NC_000019.10:40848977::G,NC_000019.10:40848977::GAG,NC_000019.10:40848977::GAGAG,NC_000019.10:40848977::GAGAGAG,NC_000019.10:40848977::GAGAGG,NC_000019.10:40848977::GAGG,NC_000019.10:40848977::GG,NC_000019.10:40848977::GGG
Gene:: CYP2A6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAG=0./0 (ALFA)
GAGAGG=0.00006/1 (TOMMO)
HGVS:: NC_000019.10:g.40848977_40848978insG, NC_000019.10:g.40848977_40848978insGAG, NC_000019.10:g.40848977_40848978insGAGAG, NC_000019.10:g.40848977_40848978insGAGAGAG, NC_000019.10:g.40848977_40848978insGAGAGG, NC_000019.10:g.40848977_40848978insGAGG, NC_000019.10:g.40848977_40848978insGG, NC_000019.10:g.40848977_40848978insGGG, NC_000019.9:g.41354882_41354883insG, NC_000019.9:g.41354882_41354883insGAG, NC_000019.9:g.41354882_41354883insGAGAG, NC_000019.9:g.41354882_41354883insGAGAGAG, NC_000019.9:g.41354882_41354883insGAGAGG, NC_000019.9:g.41354882_41354883insGAGG, NC_000019.9:g.41354882_41354883insGG, NC_000019.9:g.41354882_41354883insGGG, NG_008377.1:g.6470_6471insC, NG_008377.1:g.6470_6471insCTC, NG_008377.1:g.6470_6471insCTCTC, NG_008377.1:g.6470_6471insCTCTCTC, NG_008377.1:g.6470_6471insCCTCTC, NG_008377.1:g.6470_6471insCCTC, NG_008377.1:g.6470_6471insCC, NG_008377.1:g.6470_6471insCCC

Select item 14913721663.

rs1491372166 has merged into rs67032351 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGAGAGAGAGAGAGAGAGA>-,GA,GAGA,GAGAGA,GAGAGAGA,GAGAGAGAGA,GAGAGAGAGAGA,GAGAGAGAGAGAGA,GAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA [Show Flanks]
Chromosome:: 19:40848958 (GRCh38)
19:41354863 (GRCh37)
Canonical SPDI:: NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40848940:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA
Gene:: CYP2A6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAGAGAGAGAGAGAGAGA=0./0 (ALFA)
AGAG=0.3263/1634 (1000Genomes)
HGVS:: NC_000019.10:g.40848942GA[8], NC_000019.10:g.40848942GA[9], NC_000019.10:g.40848942GA[10], NC_000019.10:g.40848942GA[11], NC_000019.10:g.40848942GA[12], NC_000019.10:g.40848942GA[13], NC_000019.10:g.40848942GA[14], NC_000019.10:g.40848942GA[15], NC_000019.10:g.40848942GA[16], NC_000019.10:g.40848942GA[17], NC_000019.10:g.40848942GA[19], NC_000019.10:g.40848942GA[20], NC_000019.10:g.40848942GA[21], NC_000019.10:g.40848942GA[22], NC_000019.10:g.40848942GA[23], NC_000019.10:g.40848942GA[24], NC_000019.10:g.40848942GA[25], NC_000019.10:g.40848942GA[26], NC_000019.10:g.40848942GA[27], NC_000019.9:g.41354847GA[8], NC_000019.9:g.41354847GA[9], NC_000019.9:g.41354847GA[10], NC_000019.9:g.41354847GA[11], NC_000019.9:g.41354847GA[12], NC_000019.9:g.41354847GA[13], NC_000019.9:g.41354847GA[14], NC_000019.9:g.41354847GA[15], NC_000019.9:g.41354847GA[16], NC_000019.9:g.41354847GA[17], NC_000019.9:g.41354847GA[19], NC_000019.9:g.41354847GA[20], NC_000019.9:g.41354847GA[21], NC_000019.9:g.41354847GA[22], NC_000019.9:g.41354847GA[23], NC_000019.9:g.41354847GA[24], NC_000019.9:g.41354847GA[25], NC_000019.9:g.41354847GA[26], NC_000019.9:g.41354847GA[27], NG_008377.1:g.6472CT[8], NG_008377.1:g.6472CT[9], NG_008377.1:g.6472CT[10], NG_008377.1:g.6472CT[11], NG_008377.1:g.6472CT[12], NG_008377.1:g.6472CT[13], NG_008377.1:g.6472CT[14], NG_008377.1:g.6472CT[15], NG_008377.1:g.6472CT[16], NG_008377.1:g.6472CT[17], NG_008377.1:g.6472CT[19], NG_008377.1:g.6472CT[20], NG_008377.1:g.6472CT[21], NG_008377.1:g.6472CT[22], NG_008377.1:g.6472CT[23], NG_008377.1:g.6472CT[24], NG_008377.1:g.6472CT[25], NG_008377.1:g.6472CT[26], NG_008377.1:g.6472CT[27]

Select item 14912955864.

rs1491295586 has merged into rs1440289322 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGAG>-,AG [Show Flanks]
Chromosome:: 19:40849018 (GRCh38)
19:41354923 (GRCh37)
Canonical SPDI:: NC_000019.10:40849011:AGAGAGAGAG:AGAGAG,NC_000019.10:40849011:AGAGAGAGAG:AGAGAGAG
Gene:: CYP2A6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAGAGAG=0./0 (ALFA)
-=0.00002/1 (GnomAD)
HGVS:: NC_000019.10:g.40849012AG[3], NC_000019.10:g.40849012AG[4], NC_000019.9:g.41354917AG[3], NC_000019.9:g.41354917AG[4], NG_008377.1:g.6427CT[3], NG_008377.1:g.6427CT[4]

Select item 14912849965.

rs1491284996 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GAGAGAGAG [Show Flanks]
Chromosome:: 19:40849012 (GRCh38)
19:41354918 (GRCh37)
Canonical SPDI:: NC_000019.10:40849012:GAGAGAGAGGAGAGAGAG:GAGAGAGAGGAGAGAGAGGAGAGAGAG
Gene:: CYP2A6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GAGAGAGAGGAGAGAGAGGAGAGAGAG=0.00008/1 (ALFA)
HGVS:: NC_000019.10:g.40849013GAGAGAGAG[3], NC_000019.9:g.41354918GAGAGAGAG[3], NG_008377.1:g.6418CTCTCTCTC[3]

Select item 14911203066.

rs1491120306 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 19:40848977 (GRCh38)
19:41354882 (GRCh37)
Canonical SPDI:: NC_000019.10:40848976:AA:
Gene:: CYP2A6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00172/143 (GnomAD)
HGVS:: NC_000019.10:g.40848977_40848978del, NC_000019.9:g.41354882_41354883del, NG_008377.1:g.6470_6471del

Select item 14908762957.

rs1490876295 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 19:40842189 (GRCh38)
19:41348094 (GRCh37)
Canonical SPDI:: NC_000019.10:40842188:A:C,NC_000019.10:40842188:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.40842189A>C, NC_000019.10:g.40842189A>G, NC_000019.9:g.41348094A>C, NC_000019.9:g.41348094A>G, NG_008377.1:g.13259T>G, NG_008377.1:g.13259T>C

Select item 14908576508.

rs1490857650 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:40846973 (GRCh38)
19:41352878 (GRCh37)
Canonical SPDI:: NC_000019.10:40846972:C:T
Gene:: CYP2A6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000019.10:g.40846973C>T, NC_000019.9:g.41352878C>T, NG_008377.1:g.8475G>A, NM_000762.6:c.733G>A, NM_000762.5:c.733G>A, NP_000753.3:p.Glu245Lys

Select item 14908006479.

rs1490800647 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:40855222 (GRCh38)
19:41361127 (GRCh37)
Canonical SPDI:: NC_000019.10:40855221:T:G
Validated:: by frequency,by alfa
MAF:: G=0.00007/1 (ALFA)
HGVS:: NC_000019.10:g.40855222T>G, NC_000019.9:g.41361127T>G, NG_008377.1:g.226A>C, NG_055456.1:g.4897T>G

Select item 149061411610.

rs1490614116 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 19:40852295 (GRCh38)
19:41358200 (GRCh37)
Canonical SPDI:: NC_000019.10:40852294:A:C,NC_000019.10:40852294:A:T
Gene:: CYP2A6 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.40852295A>C, NC_000019.10:g.40852295A>T, NC_000019.9:g.41358200A>C, NC_000019.9:g.41358200A>T, NG_008377.1:g.3153T>G, NG_008377.1:g.3153T>A, NG_055456.1:g.1970A>C, NG_055456.1:g.1970A>T

Select item 149038406611.

rs1490384066 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:40852868 (GRCh38)
19:41358773 (GRCh37)
Canonical SPDI:: NC_000019.10:40852867:G:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.40852868G>C, NC_000019.9:g.41358773G>C, NG_008377.1:g.2580C>G, NG_055456.1:g.2543G>C

Select item 149019386412.

rs1490193864 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:40852542 (GRCh38)
19:41358447 (GRCh37)
Canonical SPDI:: NC_000019.10:40852541:C:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000019.10:g.40852542C>A, NC_000019.9:g.41358447C>A, NG_008377.1:g.2906G>T, NG_055456.1:g.2217C>A

Select item 148966767913.

rs1489667679 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 19:40843411 (GRCh38)
19:41349316 (GRCh37)
Canonical SPDI:: NC_000019.10:40843410:C:A,NC_000019.10:40843410:C:T
Gene:: CYP2A6 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000019.10:g.40843411C>A, NC_000019.10:g.40843411C>T, NC_000019.9:g.41349316C>A, NC_000019.9:g.41349316C>T, NG_008377.1:g.12037G>T, NG_008377.1:g.12037G>A

Select item 148952531314.

rs1489525313 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:40852427 (GRCh38)
19:41358332 (GRCh37)
Canonical SPDI:: NC_000019.10:40852426:C:T
Gene:: CYP2A6 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000169/2 (ALFA)
T=0.000114/16 (GnomAD)
T=0.000781/5 (1000Genomes)
HGVS:: NC_000019.10:g.40852427C>T, NC_000019.9:g.41358332C>T, NG_008377.1:g.3021G>A, NG_055456.1:g.2102C>T

Select item 148950673615.

rs1489506736 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:40845490 (GRCh38)
19:41351395 (GRCh37)
Canonical SPDI:: NC_000019.10:40845489:G:C
Gene:: CYP2A6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.40845490G>C, NC_000019.9:g.41351395G>C, NG_008377.1:g.9958C>G

Select item 148943342416.

rs1489433424 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:40851683 (GRCh38)
19:41357588 (GRCh37)
Canonical SPDI:: NC_000019.10:40851682:G:A
Gene:: CYP2A6 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.40851683G>A, NC_000019.9:g.41357588G>A, NG_008377.1:g.3765C>T, NG_055456.1:g.1358G>A

Select item 148941845817.

rs1489418458 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:40852462 (GRCh38)
19:41358367 (GRCh37)
Canonical SPDI:: NC_000019.10:40852461:T:C
Validated:: by frequency,by alfa
MAF:: C=0.000084/1 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.40852462T>C, NC_000019.9:g.41358367T>C, NG_008377.1:g.2986A>G, NG_055456.1:g.2137T>C

Select item 148940508318.

rs1489405083 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 19:40854150 (GRCh38)
19:41360055 (GRCh37)
Canonical SPDI:: NC_000019.10:40854149:G:A,NC_000019.10:40854149:G:C,NC_000019.10:40854149:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
T=0.000004/1 (TOPMED)
G=0.333333/2 (SGDP_PRJ)
HGVS:: NC_000019.10:g.40854150G>A, NC_000019.10:g.40854150G>C, NC_000019.10:g.40854150G>T, NC_000019.9:g.41360055G>A, NC_000019.9:g.41360055G>C, NC_000019.9:g.41360055G>T, NG_008377.1:g.1298C>T, NG_008377.1:g.1298C>G, NG_008377.1:g.1298C>A, NG_055456.1:g.3825G>A, NG_055456.1:g.3825G>C, NG_055456.1:g.3825G>T

Select item 148917877919.

rs1489178779 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 19:40848987 (GRCh38)
19:41354892 (GRCh37)
Canonical SPDI:: NC_000019.10:40848986:G:A,NC_000019.10:40848986:G:C
Gene:: CYP2A6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00481/57 (ALFA)
A=0.00079/16 (TOMMO)
A=0.00368/309 (GnomAD)
A=0.00499/14 (KOREAN)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000019.10:g.40848987G>A, NC_000019.10:g.40848987G>C, NC_000019.9:g.41354892G>A, NC_000019.9:g.41354892G>C, NG_008377.1:g.6461C>T, NG_008377.1:g.6461C>G

Select item 148913999420.

rs1489139994 has merged into rs1164660108 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA>-,GAGA,GAGAGA,GAGAGAGAGAGAGA,GAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA [Show Flanks]
Chromosome:: 19:40849058 (GRCh38)
19:41354963 (GRCh37)
Canonical SPDI:: NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000019.10:40849045:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA:GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA
Gene:: CYP2A6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAGAGAGAGAGAGAGAGAGAGAGAGA=0./0 (ALFA)
HGVS:: NC_000019.10:g.40849046GA[6], NC_000019.10:g.40849046GA[8], NC_000019.10:g.40849046GA[9], NC_000019.10:g.40849046GA[13], NC_000019.10:g.40849046GA[14], NC_000019.10:g.40849046GA[15], NC_000019.10:g.40849046GA[16], NC_000019.10:g.40849046GA[17], NC_000019.10:g.40849046GA[18], NC_000019.10:g.40849046GA[19], NC_000019.10:g.40849046GA[20], NC_000019.10:g.40849046GA[21], NC_000019.10:g.40849046GA[23], NC_000019.10:g.40849046GA[24], NC_000019.10:g.40849046GA[25], NC_000019.10:g.40849046GA[26], NC_000019.10:g.40849046GA[27], NC_000019.10:g.40849046GA[30], NC_000019.10:g.40849046GA[31], NC_000019.10:g.40849046GA[32], NC_000019.9:g.41354951GA[6], NC_000019.9:g.41354951GA[8], NC_000019.9:g.41354951GA[9], NC_000019.9:g.41354951GA[13], NC_000019.9:g.41354951GA[14], NC_000019.9:g.41354951GA[15], NC_000019.9:g.41354951GA[16], NC_000019.9:g.41354951GA[17], NC_000019.9:g.41354951GA[18], NC_000019.9:g.41354951GA[19], NC_000019.9:g.41354951GA[20], NC_000019.9:g.41354951GA[21], NC_000019.9:g.41354951GA[23], NC_000019.9:g.41354951GA[24], NC_000019.9:g.41354951GA[25], NC_000019.9:g.41354951GA[26], NC_000019.9:g.41354951GA[27], NC_000019.9:g.41354951GA[30], NC_000019.9:g.41354951GA[31], NC_000019.9:g.41354951GA[32], NG_008377.1:g.6359TC[6], NG_008377.1:g.6359TC[8], NG_008377.1:g.6359TC[9], NG_008377.1:g.6359TC[13], NG_008377.1:g.6359TC[14], NG_008377.1:g.6359TC[15], NG_008377.1:g.6359TC[16], NG_008377.1:g.6359TC[17], NG_008377.1:g.6359TC[18], NG_008377.1:g.6359TC[19], NG_008377.1:g.6359TC[20], NG_008377.1:g.6359TC[21], NG_008377.1:g.6359TC[23], NG_008377.1:g.6359TC[24], NG_008377.1:g.6359TC[25], NG_008377.1:g.6359TC[26], NG_008377.1:g.6359TC[27], NG_008377.1:g.6359TC[30], NG_008377.1:g.6359TC[31], NG_008377.1:g.6359TC[32]

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