SNP Links for Gene (Select 54055) - SNP

Links from Gene

Items: 1 to 20 of 2672

<< First< Prev

Page of 134

Next >Last >>

Select item 14908646971.

rs1490864697 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:13844505 (GRCh38)
21:15216826 (GRCh37)
Canonical SPDI:: NC_000021.9:13844504:G:A
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.1531/684 (ALFA)
HGVS:: NC_000021.9:g.13844505G>A, NC_000021.8:g.15216826G>A

Select item 14908371992.

rs1490837199 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 21:13845221 (GRCh38)
21:15217542 (GRCh37)
Canonical SPDI:: NC_000021.9:13845220:T:A,NC_000021.9:13845220:T:C
Gene:: CYP4F29P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.02264/343 (ALFA)
A=0.000007/1 (GnomAD)
C=0.13655/399 (KOREAN)
HGVS:: NC_000021.9:g.13845221T>A, NC_000021.9:g.13845221T>C, NC_000021.8:g.15217542T>A, NC_000021.8:g.15217542T>C, NR_026755.1:n.649A>T, NR_026755.1:n.649A>G

Select item 14906689373.

rs1490668937 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 21:13844817 (GRCh38)
21:15217138 (GRCh37)
Canonical SPDI:: NC_000021.9:13844816:T:G
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000021.9:g.13844817T>G, NC_000021.8:g.15217138T>G

Select item 14905373414.

rs1490537341 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:13846994 (GRCh38)
21:15219315 (GRCh37)
Canonical SPDI:: NC_000021.9:13846993:T:C
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.13846994T>C, NC_000021.8:g.15219315T>C

Select item 14900788395.

rs1490078839 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:13847378 (GRCh38)
21:15219699 (GRCh37)
Canonical SPDI:: NC_000021.9:13847377:T:C
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000021.9:g.13847378T>C, NC_000021.8:g.15219699T>C

Select item 14893215146.

rs1489321514 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:13846334 (GRCh38)
21:15218655 (GRCh37)
Canonical SPDI:: NC_000021.9:13846333:A:G
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000021.9:g.13846334A>G, NC_000021.8:g.15218655A>G

Select item 14890782837.

rs1489078283 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 21:13845990 (GRCh38)
21:15218311 (GRCh37)
Canonical SPDI:: NC_000021.9:13845989:G:C
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000214/3 (ALFA)
C=0.000036/5 (GnomAD)
C=0.000057/15 (TOPMED)
HGVS:: NC_000021.9:g.13845990G>C, NC_000021.8:g.15218311G>C

Select item 14890488768.

rs1489048876 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:13848338 (GRCh38)
21:15220659 (GRCh37)
Canonical SPDI:: NC_000021.9:13848337:C:T
Gene:: CYP4F29P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.13848338C>T, NC_000021.8:g.15220659C>T, NR_026755.1:n.27G>A

Select item 14887913879.

rs1488791387 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 21:13845574 (GRCh38)
21:15217895 (GRCh37)
Canonical SPDI:: NC_000021.9:13845573:T:C,NC_000021.9:13845573:T:G
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
C=0.000156/1 (1000Genomes)
HGVS:: NC_000021.9:g.13845574T>C, NC_000021.9:g.13845574T>G, NC_000021.8:g.15217895T>C, NC_000021.8:g.15217895T>G

Select item 148860826210.

rs1488608262 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:13846258 (GRCh38)
21:15218579 (GRCh37)
Canonical SPDI:: NC_000021.9:13846257:A:G
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.0013/6 (ALFA)
G=0.0209/61 (KOREAN)
HGVS:: NC_000021.9:g.13846258A>G, NC_000021.8:g.15218579A>G

Select item 148853915611.

rs1488539156 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 21:13843593 (GRCh38)
21:15215914 (GRCh37)
Canonical SPDI:: NC_000021.9:13843592:G:T
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_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_000021.9:g.13843593G>T, NC_000021.8:g.15215914G>T

Select item 148842192412.

rs1488421924 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 21:13846822 (GRCh38)
21:15219143 (GRCh37)
Canonical SPDI:: NC_000021.9:13846821:GGG:GG
Gene:: CYP4F29P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GG=0.0007/3 (ALFA)
HGVS:: NC_000021.9:g.13846824del, NC_000021.8:g.15219145del, NR_026755.1:n.403del

Select item 148833035513.

rs1488330355 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:13847830 (GRCh38)
21:15220151 (GRCh37)
Canonical SPDI:: NC_000021.9:13847829:G:A
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.13847830G>A, NC_000021.8:g.15220151G>A

Select item 148791818714.

rs1487918187 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 21:13848179 (GRCh38)
21:15220500 (GRCh37)
Canonical SPDI:: NC_000021.9:13848178:G:A,NC_000021.9:13848178:G:T
Gene:: CYP4F29P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00246/11 (ALFA)
T=0.00007/1 (TOMMO)
HGVS:: NC_000021.9:g.13848179G>A, NC_000021.9:g.13848179G>T, NC_000021.8:g.15220500G>A, NC_000021.8:g.15220500G>T, NR_026755.1:n.186C>T, NR_026755.1:n.186C>A

Select item 148760237615.

rs1487602376 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 21:13846723 (GRCh38)
21:15219044 (GRCh37)
Canonical SPDI:: NC_000021.9:13846722:G:A,NC_000021.9:13846722:G:C,NC_000021.9:13846722:G:T
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.45973/1347 (KOREAN)
HGVS:: NC_000021.9:g.13846723G>A, NC_000021.9:g.13846723G>C, NC_000021.9:g.13846723G>T, NC_000021.8:g.15219044G>A, NC_000021.8:g.15219044G>C, NC_000021.8:g.15219044G>T

Select item 148759391716.

rs1487593917 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:13847718 (GRCh38)
21:15220039 (GRCh37)
Canonical SPDI:: NC_000021.9:13847717:C:T
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.0018/8 (ALFA)
HGVS:: NC_000021.9:g.13847718C>T, NC_000021.8:g.15220039C>T

Select item 148737272817.

rs1487372728 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:13843047 (GRCh38)
21:15215368 (GRCh37)
Canonical SPDI:: NC_000021.9:13843046:A:G
Gene:: CYP4F29P (Varview)
Functional Consequence:: 500B_downstream_variant,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_000021.9:g.13843047A>G, NC_000021.8:g.15215368A>G

Select item 148694389518.

rs1486943895 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 21:13847602 (GRCh38)
21:15219923 (GRCh37)
Canonical SPDI:: NC_000021.9:13847601:C:A
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.13847602C>A, NC_000021.8:g.15219923C>A

Select item 148693323619.

rs1486933236 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 21:13848670 (GRCh38)
21:15220991 (GRCh37)
Canonical SPDI:: NC_000021.9:13848669:A:T
Gene:: CYP4F29P (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000021.9:g.13848670A>T, NC_000021.8:g.15220991A>T

Select item 148666508420.

rs1486665084 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 21:13844743 (GRCh38)
21:15217064 (GRCh37)
Canonical SPDI:: NC_000021.9:13844742:G:A,NC_000021.9:13844742:G:T
Gene:: CYP4F29P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000054/1 (ALFA)
T=0.000029/4 (GnomAD)
HGVS:: NC_000021.9:g.13844743G>A, NC_000021.9:g.13844743G>T, NC_000021.8:g.15217064G>A, NC_000021.8:g.15217064G>T

<< First< Prev

Page of 134

Next >Last >>

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 2672

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity