SNP Links for Gene (Select 148932) - SNP

Links from Gene

Items: 1 to 20 of 2558

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Select item 14908950021.

rs1490895002 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:46610476 (GRCh38)
1:47076148 (GRCh37)
Canonical SPDI:: NC_000001.11:46610475:C:G
Gene:: MOB3C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000001.11:g.46610476C>G, NC_000001.10:g.47076148C>G, NG_027514.1:g.11416G>C

Select item 14908572442.

rs1490857244 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:46609209 (GRCh38)
1:47074881 (GRCh37)
Canonical SPDI:: NC_000001.11:46609208:T:G
Gene:: MOB3C (Varview)
Functional Consequence:: 3_prime_UTR_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.46609209T>G, NC_000001.10:g.47074881T>G, NG_032029.2:g.86A>C, NG_027514.1:g.12683A>C, NM_145279.5:c.*446A>C, NM_145279.4:c.*446A>C, NM_201403.3:c.*446A>C, NM_201403.2:c.*446A>C

Select item 14899775193.

rs1489977519 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:46615014 (GRCh38)
1:47080686 (GRCh37)
Canonical SPDI:: NC_000001.11:46615013:C:T
Gene:: MOB3C (Varview)
Functional Consequence:: intron_variant,5_prime_UTR_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.46615014C>T, NC_000001.10:g.47080686C>T, NG_027514.1:g.6878G>A, NM_145279.5:c.-94G>A, NM_145279.4:c.63G>A

Select item 14899117734.

rs1489911773 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:46612910 (GRCh38)
1:47078582 (GRCh37)
Canonical SPDI:: NC_000001.11:46612909:G:T
Gene:: MOB3C (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.46612910G>T, NC_000001.10:g.47078582G>T, NG_027514.1:g.8982C>A, NM_145279.5:c.412C>A, NM_145279.4:c.568C>A, NM_201403.3:c.412C>A, NM_201403.2:c.412C>A, NP_660322.3:p.Arg138Ser, NP_958805.1:p.Arg138Ser

Select item 14899111735.

rs1489911173 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:46612686 (GRCh38)
1:47078358 (GRCh37)
Canonical SPDI:: NC_000001.11:46612685:G:A
Gene:: MOB3C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00219/37 (TOMMO)
A=0.04004/117 (KOREAN)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000001.11:g.46612686G>A, NC_000001.10:g.47078358G>A, NG_027514.1:g.9206C>T

Select item 14898800836.

rs1489880083 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:46608095 (GRCh38)
1:47073767 (GRCh37)
Canonical SPDI:: NC_000001.11:46608094:G:A
Gene:: MOB3C (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.46608095G>A, NC_000001.10:g.47073767G>A, NG_032029.2:g.1200C>T, NG_027514.1:g.13797C>T, NM_145279.5:c.*1560C>T, NM_145279.4:c.*1560C>T, NM_201403.3:c.*1560C>T, NM_201403.2:c.*1560C>T

Select item 14896801797.

rs1489680179 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:46611575 (GRCh38)
1:47077247 (GRCh37)
Canonical SPDI:: NC_000001.11:46611574:C:T
Gene:: MOB3C (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_000001.11:g.46611575C>T, NC_000001.10:g.47077247C>T, NG_027514.1:g.10317G>A

Select item 14893638598.

rs1489363859 [Homo sapiens]

Variant type:: DELINS
Alleles:: AACT>- [Show Flanks]
Chromosome:: 1:46617007 (GRCh38)
1:47082679 (GRCh37)
Canonical SPDI:: NC_000001.11:46617003:ACTAACT:ACT
Gene:: MOB3C (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: ACT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.46617007_46617010del, NC_000001.10:g.47082679_47082682del, NG_027514.1:g.4885_4888del

Select item 14892983909.

rs1489298390 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAAA>- [Show Flanks]
Chromosome:: 1:46612658 (GRCh38)
1:47078330 (GRCh37)
Canonical SPDI:: NC_000001.11:46612654:AAAGAAA:AAA
Gene:: MOB3C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.46612658_46612661del, NC_000001.10:g.47078330_47078333del, NG_027514.1:g.9234_9237del

Select item 148839590610.

rs1488395906 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 1:46609986 (GRCh38)
1:47075658 (GRCh37)
Canonical SPDI:: NC_000001.11:46609985:T:C,NC_000001.11:46609985:T:G
Gene:: MOB3C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
G=0.008197/15 (Korea1K)
HGVS:: NC_000001.11:g.46609986T>C, NC_000001.11:g.46609986T>G, NC_000001.10:g.47075658T>C, NC_000001.10:g.47075658T>G, NG_027514.1:g.11906A>G, NG_027514.1:g.11906A>C

Select item 148798543211.

rs1487985432 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:46607261 (GRCh38)
1:47072933 (GRCh37)
Canonical SPDI:: NC_000001.11:46607260:A:G
Gene:: MOB3C (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.00007/1 (ALFA)
HGVS:: NC_000001.11:g.46607261A>G, NC_000001.10:g.47072933A>G, NG_032029.2:g.2034T>C, NG_027514.1:g.14631T>C

Select item 148771667512.

rs1487716675 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:46610527 (GRCh38)
1:47076199 (GRCh37)
Canonical SPDI:: NC_000001.11:46610526:A:G
Gene:: MOB3C (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)
HGVS:: NC_000001.11:g.46610527A>G, NC_000001.10:g.47076199A>G, NG_027514.1:g.11365T>C

Select item 148718372913.

rs1487183729 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:46613738 (GRCh38)
1:47079410 (GRCh37)
Canonical SPDI:: NC_000001.11:46613737:C:T
Gene:: MOB3C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.46613738C>T, NC_000001.10:g.47079410C>T, NG_027514.1:g.8154G>A

Select item 148709420714.

rs1487094207 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:46615787 (GRCh38)
1:47081459 (GRCh37)
Canonical SPDI:: NC_000001.11:46615786:G:A
Gene:: MOB3C (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.46615787G>A, NC_000001.10:g.47081459G>A, NG_027514.1:g.6105C>T

Select item 148644447915.

rs1486444479 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:46616473 (GRCh38)
1:47082145 (GRCh37)
Canonical SPDI:: NC_000001.11:46616472:T:C
Gene:: MOB3C (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.46616473T>C, NC_000001.10:g.47082145T>C, NG_027514.1:g.5419A>G

Select item 148621382116.

rs1486213821 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:46618206 (GRCh38)
1:47083878 (GRCh37)
Canonical SPDI:: NC_000001.11:46618205:G:C
Gene:: MOB3C (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000001.11:g.46618206G>C, NC_000001.10:g.47083878G>C, NG_027514.1:g.3686C>G

Select item 148612153517.

rs1486121535 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:46617291 (GRCh38)
1:47082963 (GRCh37)
Canonical SPDI:: NC_000001.11:46617290:A:G
Gene:: MOB3C (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
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.46617291A>G, NC_000001.10:g.47082963A>G, NG_027514.1:g.4601T>C

Select item 148594588218.

rs1485945882 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 1:46612775 (GRCh38)
1:47078447 (GRCh37)
Canonical SPDI:: NC_000001.11:46612774:CC:C
Gene:: MOB3C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.46612776del, NC_000001.10:g.47078448del, NG_027514.1:g.9117del

Select item 148561783419.

rs1485617834 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:46612457 (GRCh38)
1:47078129 (GRCh37)
Canonical SPDI:: NC_000001.11:46612456:T:C
Gene:: MOB3C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.46612457T>C, NC_000001.10:g.47078129T>C, NG_027514.1:g.9435A>G

Select item 148493477420.

rs1484934774 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:46612428 (GRCh38)
1:47078100 (GRCh37)
Canonical SPDI:: NC_000001.11:46612427:C:T
Gene:: MOB3C (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.46612428C>T, NC_000001.10:g.47078100C>T, NG_027514.1:g.9464G>A

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