SNP Links for Nucleotide (Select 22546017) - SNP

Links from Nucleotide

Items: 1 to 20 of 28

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Select item 14705097711.

rs1470509771 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>G
Chromosome:: no mapping
Canonical SPDI:

Select item 14024960712.

rs1402496071 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>A
Chromosome:: no mapping
Canonical SPDI:

Select item 13445538353.

rs1344553835 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:133350131 (GRCh38)
9:136216986 (GRCh37)
Canonical SPDI:: NC_000009.12:133350130:G:C
Gene:: RPL7A (Varview), MED22 (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.133350131G>C, NG_008477.2:g.11356C>G, NG_008477.1:g.11376C>G, NW_009646201.1:g.176225G>C, NW_003315925.1:g.176225G>C, NC_000009.11:g.136216986G>C, NR_000017.1:n.38G>C

Select item 13419158884.

rs1341915888 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:133350142 (GRCh38)
9:136216997 (GRCh37)
Canonical SPDI:: NC_000009.12:133350141:A:G
Gene:: RPL7A (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.133350142A>G, NG_008477.2:g.11345T>C, NG_008477.1:g.11365T>C, NW_009646201.1:g.176236A>G, NW_003315925.1:g.176236A>G, NC_000009.11:g.136216997A>G, NR_000017.1:n.49A>G

Select item 12611874505.

rs1261187450 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>G
Chromosome:: no mapping
Canonical SPDI:

Select item 12466738626.

rs1246673862 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 9:133350103 (GRCh38)
9:136216958 (GRCh37)
Canonical SPDI:: NC_000009.12:133350102:A:C,NC_000009.12:133350102:A:G
Gene:: RPL7A (Varview), MED22 (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000009.12:g.133350103A>C, NC_000009.12:g.133350103A>G, NG_008477.2:g.11384T>G, NG_008477.2:g.11384T>C, NG_008477.1:g.11404T>G, NG_008477.1:g.11404T>C, NW_009646201.1:g.176197A>C, NW_009646201.1:g.176197A>G, NW_003315925.1:g.176197A>C, NW_003315925.1:g.176197A>G, NC_000009.11:g.136216958A>C, NC_000009.11:g.136216958A>G, NR_000017.1:n.10A>C, NR_000017.1:n.10A>G

Select item 12394474447.

rs1239447444 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>G
Chromosome:: no mapping
Canonical SPDI:

Select item 12040896168.

rs1204089616 [Homo sapiens]

Variant type:: SNV:
Alleles:: T>C
Chromosome:: no mapping
Canonical SPDI:

Select item 11749733259.

rs1174973325 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>T
Chromosome:: no mapping
Canonical SPDI:

Select item 115809785110.

rs1158097851 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:133350119 (GRCh38)
9:136216974 (GRCh37)
Canonical SPDI:: NC_000009.12:133350118:C:G
Gene:: RPL7A (Varview), MED22 (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: G=0.00007/2 (TOMMO)
HGVS:: NC_000009.12:g.133350119C>G, NG_008477.2:g.11368G>C, NG_008477.1:g.11388G>C, NW_009646201.1:g.176213C>G, NW_003315925.1:g.176213C>G, NC_000009.11:g.136216974C>G, NR_000017.1:n.26C>G

Select item 94836621211.

rs948366212 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:133350135 (GRCh38)
9:136216990 (GRCh37)
Canonical SPDI:: NC_000009.12:133350134:A:G
Gene:: RPL7A (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.133350135A>G, NG_008477.2:g.11352T>C, NG_008477.1:g.11372T>C, NW_009646201.1:g.176229A>G, NW_003315925.1:g.176229A>G, NC_000009.11:g.136216990A>G, NR_000017.1:n.42A>G

Select item 90340971512.

rs903409715 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:133350129 (GRCh38)
9:136216984 (GRCh37)
Canonical SPDI:: NC_000009.12:133350128:C:G
Gene:: RPL7A (Varview), MED22 (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.133350129C>G, NG_008477.2:g.11358G>C, NG_008477.1:g.11378G>C, NW_009646201.1:g.176223C>G, NW_003315925.1:g.176223C>G, NC_000009.11:g.136216984C>G, NR_000017.1:n.36C>G

Select item 89414605013.

rs894146050 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 9:133350127 (GRCh38)
9:136216983 (GRCh37)
Canonical SPDI:: NC_000009.12:133350127:A:AA
Gene:: RPL7A (Varview), MED22 (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.133350128dup, NG_008477.2:g.11359dup, NG_008477.1:g.11379dup, NW_009646201.1:g.176222dup, NW_003315925.1:g.176222dup, NC_000009.11:g.136216983dup, NR_000017.1:n.35dup

Select item 78256386514.

rs782563865 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 9:133350096 (GRCh38)
9:136216951 (GRCh37)
Canonical SPDI:: NC_000009.12:133350095:T:G
Gene:: RPL7A (Varview), MED22 (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.133350096T>G, NG_008477.2:g.11391A>C, NG_008477.1:g.11411A>C, NW_009646201.1:g.176190T>G, NW_003315925.1:g.176190T>G, NC_000009.11:g.136216951T>G, NR_000017.1:n.3T>G

Select item 78252971315.

rs782529713 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:133350104 (GRCh38)
9:136216959 (GRCh37)
Canonical SPDI:: NC_000009.12:133350103:T:C
Gene:: RPL7A (Varview), MED22 (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.133350104T>C, NG_008477.2:g.11383A>G, NG_008477.1:g.11403A>G, NW_009646201.1:g.176198T>C, NW_003315925.1:g.176198T>C, NC_000009.11:g.136216959T>C, NR_000017.1:n.11T>C

Select item 78236455516.

rs782364555 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>A
Chromosome:: no mapping
Canonical SPDI:

Select item 78229007817.

rs782290078 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 9:133350098 (GRCh38)
9:136216953 (GRCh37)
Canonical SPDI:: NC_000009.12:133350097:C:G,NC_000009.12:133350097:C:T
Gene:: RPL7A (Varview), MED22 (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000009.12:g.133350098C>G, NC_000009.12:g.133350098C>T, NG_008477.2:g.11389G>C, NG_008477.2:g.11389G>A, NG_008477.1:g.11409G>C, NG_008477.1:g.11409G>A, NW_009646201.1:g.176192C>G, NW_009646201.1:g.176192C>T, NW_003315925.1:g.176192C>G, NW_003315925.1:g.176192C>T, NC_000009.11:g.136216953C>G, NC_000009.11:g.136216953C>T, NR_000017.1:n.5C>G, NR_000017.1:n.5C>T

Select item 78213911418.

rs782139114 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:133350154 (GRCh38)
9:136217009 (GRCh37)
Canonical SPDI:: NC_000009.12:133350153:T:A
Gene:: RPL7A (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.133350154T>A, NG_008477.2:g.11333A>T, NG_008477.1:g.11353A>T, NW_009646201.1:g.176248T>A, NW_003315925.1:g.176248T>A, NC_000009.11:g.136217009T>A, NR_000017.1:n.61T>A

Select item 78212011119.

rs782120111 [Homo sapiens]

Variant type:: SNV:
Alleles:: CT>-
Chromosome:: no mapping
Canonical SPDI:

Select item 78200723320.

rs782007233 has merged into rs587740824 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 9:133350150 (GRCh38)
9:136217005 (GRCh37)
Canonical SPDI:: NC_000009.12:133350149:TTTTT:TTTT
Gene:: RPL7A (Varview), SNORD36C (Varview), SNORD36B (Varview), SNORD36A (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTT=0./0 (ALFA)
-=0./0 (GnomAD)
-=0.000049/13 (TOPMED)
HGVS:: NC_000009.12:g.133350154del, NG_008477.2:g.11337del, NG_008477.1:g.11357del, NW_009646201.1:g.176248del, NW_003315925.1:g.176248del, NC_000009.11:g.136217009del, NR_000017.1:n.61del

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Items: 1 to 20 of 28

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