SNP Links for Nucleotide (Select 296080750) - SNP

Links from Nucleotide

Items: 1 to 20 of 359

<< First< Prev

Page of 18

Next >Last >>

Select item 14898794651.

rs1489879465 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:73986810 (GRCh38)
4:74852527 (GRCh37)
Canonical SPDI:: NC_000004.12:73986809:G:C
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_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_000004.12:g.73986810G>C, NC_000004.11:g.74852527G>C, NG_032897.1:g.315C>G, NM_002704.3:c.*462C>G

Select item 14840305272.

rs1484030527 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:73987347 (GRCh38)
4:74853064 (GRCh37)
Canonical SPDI:: NC_000004.12:73987346:G:A
Gene:: PPBP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.73987347G>A, NC_000004.11:g.74853064G>A, NM_002704.3:c.312C>T

Select item 14840202403.

rs1484020240 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:73986892 (GRCh38)
4:74852609 (GRCh37)
Canonical SPDI:: NC_000004.12:73986891:A:G
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.73986892A>G, NC_000004.11:g.74852609A>G, NG_032897.1:g.233T>C, NM_002704.3:c.*380T>C

Select item 14828046044.

rs1482804604 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 4:73986466 (GRCh38)
4:74852183 (GRCh37)
Canonical SPDI:: NC_000004.12:73986465:A:C,NC_000004.12:73986465:A:G
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.73986466A>C, NC_000004.12:g.73986466A>G, NC_000004.11:g.74852183A>C, NC_000004.11:g.74852183A>G, NG_032897.1:g.659T>G, NG_032897.1:g.659T>C, NM_002704.3:c.*806T>G, NM_002704.3:c.*806T>C

Select item 14806731265.

rs1480673126 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:73987259 (GRCh38)
4:74852976 (GRCh37)
Canonical SPDI:: NC_000004.12:73987258:G:T
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.73987259G>T, NC_000004.11:g.74852976G>T, NM_002704.3:c.*13C>A

Select item 14795070856.

rs1479507085 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:73986888 (GRCh38)
4:74852605 (GRCh37)
Canonical SPDI:: NC_000004.12:73986887:C:A
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_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_000004.12:g.73986888C>A, NC_000004.11:g.74852605C>A, NG_032897.1:g.237G>T, NM_002704.3:c.*384G>T

Select item 14745258727.

rs1474525872 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:73987172 (GRCh38)
4:74852889 (GRCh37)
Canonical SPDI:: NC_000004.12:73987171:T:A
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000021/3 (GnomAD)
HGVS:: NC_000004.12:g.73987172T>A, NC_000004.11:g.74852889T>A, NM_002704.3:c.*100A>T

Select item 14726624568.

rs1472662456 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:73987360 (GRCh38)
4:74853077 (GRCh37)
Canonical SPDI:: NC_000004.12:73987359:T:C
Gene:: PPBP (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.73987360T>C, NC_000004.11:g.74853077T>C, NM_002704.3:c.299A>G, NP_002695.1:p.Asp100Gly

Select item 14702253249.

rs1470225324 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:73988080 (GRCh38)
4:74853797 (GRCh37)
Canonical SPDI:: NC_000004.12:73988079:G:T
Gene:: PPBP (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
T=0.000035/1 (TOMMO)
HGVS:: NC_000004.12:g.73988080G>T, NC_000004.11:g.74853797G>T, NM_002704.3:c.24C>A

Select item 146577209810.

rs1465772098 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:73987252 (GRCh38)
4:74852969 (GRCh37)
Canonical SPDI:: NC_000004.12:73987251:T:A
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.73987252T>A, NC_000004.11:g.74852969T>A, NM_002704.3:c.*20A>T

Select item 146308792211.

rs1463087922 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:73986985 (GRCh38)
4:74852702 (GRCh37)
Canonical SPDI:: NC_000004.12:73986984:G:C
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.73986985G>C, NC_000004.11:g.74852702G>C, NG_032897.1:g.140C>G, NM_002704.3:c.*287C>G

Select item 146139299512.

rs1461392995 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:73987644 (GRCh38)
4:74853361 (GRCh37)
Canonical SPDI:: NC_000004.12:73987643:G:A
Gene:: PPBP (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.73987644G>A, NC_000004.11:g.74853361G>A, NM_002704.3:c.157C>T

Select item 145771447713.

rs1457714477 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:73987299 (GRCh38)
4:74853016 (GRCh37)
Canonical SPDI:: NC_000004.12:73987298:T:A
Gene:: PPBP (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.73987299T>A, NC_000004.11:g.74853016T>A, NM_002704.3:c.360A>T, NP_002695.1:p.Lys120Asn

Select item 145515263914.

rs1455152639 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:73986552 (GRCh38)
4:74852269 (GRCh37)
Canonical SPDI:: NC_000004.12:73986551:A:G
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000004.12:g.73986552A>G, NC_000004.11:g.74852269A>G, NG_032897.1:g.573T>C, NM_002704.3:c.*720T>C

Select item 145381119215.

rs1453811192 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 4:73986600 (GRCh38)
4:74852317 (GRCh37)
Canonical SPDI:: NC_000004.12:73986599:G:C,NC_000004.12:73986599:G:T
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.73986600G>C, NC_000004.12:g.73986600G>T, NC_000004.11:g.74852317G>C, NC_000004.11:g.74852317G>T, NG_032897.1:g.525C>G, NG_032897.1:g.525C>A, NM_002704.3:c.*672C>G, NM_002704.3:c.*672C>A

Select item 144699963816.

rs1446999638 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:73988087 (GRCh38)
4:74853804 (GRCh37)
Canonical SPDI:: NC_000004.12:73988086:T:C
Gene:: PPBP (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000004.12:g.73988087T>C, NC_000004.11:g.74853804T>C, NM_002704.3:c.17A>G, NP_002695.1:p.Asp6Gly

Select item 144690409317.

rs1446904093 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:73987334 (GRCh38)
4:74853051 (GRCh37)
Canonical SPDI:: NC_000004.12:73987333:C:T
Gene:: PPBP (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.0001/1 (ALFA)
HGVS:: NC_000004.12:g.73987334C>T, NC_000004.11:g.74853051C>T, NM_002704.3:c.325G>A, NP_002695.1:p.Asp109Asn

Select item 144681845518.

rs1446818455 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:73987158 (GRCh38)
4:74852875 (GRCh37)
Canonical SPDI:: NC_000004.12:73987157:A:G
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000004.12:g.73987158A>G, NC_000004.11:g.74852875A>G, NM_002704.3:c.*114T>C

Select item 144501055019.

rs1445010550 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:73986667 (GRCh38)
4:74852384 (GRCh37)
Canonical SPDI:: NC_000004.12:73986666:C:T
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_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_000004.12:g.73986667C>T, NC_000004.11:g.74852384C>T, NG_032897.1:g.458G>A, NM_002704.3:c.*605G>A

Select item 144294850920.

rs1442948509 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:73987216 (GRCh38)
4:74852933 (GRCh37)
Canonical SPDI:: NC_000004.12:73987215:G:T
Gene:: PPBP (Varview)
Functional Consequence:: 3_prime_UTR_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_000004.12:g.73987216G>T, NC_000004.11:g.74852933G>T, NM_002704.3:c.*56C>A

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 359

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity