SNP Links for Gene (Select 90933) - SNP

Links from Gene

Items: 1 to 20 of 4762

<< First< Prev

Page of 239

Next >Last >>

Select item 14913378811.

rs1491337881 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GAAAAAAAA,GAAAAAAAAAAA,GAAAAAAAAAAAA [Show Flanks]
Chromosome:: 5:181228558 (GRCh38)
5:180655559 (GRCh37)
Canonical SPDI:: NC_000005.10:181228558:AAAAAAAA:AAAAAAAAGAAAAAAAA,NC_000005.10:181228558:AAAAAAAA:AAAAAAAAGAAAAAAAAAAA,NC_000005.10:181228558:AAAAAAAA:AAAAAAAAGAAAAAAAAAAAA
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAGAAAAAAAAAAA=0.00008/1 (ALFA)
HGVS:: NC_000005.10:g.181228559_181228566A[8]GAAAAAAAA[1], NC_000005.10:g.181228559_181228566A[8]GAAAAAAAAAAA[1], NC_000005.10:g.181228559_181228566A[8]GAAAAAAAAAAAA[1], NC_000005.9:g.180655559_180655566A[8]GAAAAAAAA[1], NC_000005.9:g.180655559_180655566A[8]GAAAAAAAAAAA[1], NC_000005.9:g.180655559_180655566A[8]GAAAAAAAAAAAA[1], NG_030346.1:g.10297_10304A[8]GAAAAAAAA[1], NG_030346.1:g.10297_10304A[8]GAAAAAAAAAAA[1], NG_030346.1:g.10297_10304A[8]GAAAAAAAAAAAA[1]

Select item 14911061732.

rs1491106173 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 5:181228558 (GRCh38)
5:180655558 (GRCh37)
Canonical SPDI:: NC_000005.10:181228557:CA:
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00059/7 (ALFA)
HGVS:: NC_000005.10:g.181228558_181228559del, NC_000005.9:g.180655558_180655559del, NG_030346.1:g.10296_10297del

Select item 14910731603.

rs1491073160 has merged into rs139637485 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>-,GTGT [Show Flanks]
Chromosome:: 5:181223839 (GRCh38)
5:180650839 (GRCh37)
Canonical SPDI:: NC_000005.10:181223835:TGTGT:TGT,NC_000005.10:181223835:TGTGT:TGTGTGT
Gene:: TRIM41 (Varview), MIR4638 (Varview)
Functional Consequence:: 5_prime_UTR_variant,upstream_transcript_variant,non_coding_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGT=0.02072/307 (ALFA)
TG=0.00952/2 (Vietnamese)
TG=0.01784/299 (TOMMO)
TG=0.025/1 (GENOME_DK)
TG=0.02675/49 (Korea1K)
TG=0.04167/25 (NorthernSweden)
TG=0.05631/217 (ALSPAC)
TG=0.06365/236 (TWINSUK)
TG=0.06853/307 (Estonian)
TG=0.24532/1229 (1000Genomes)
HGVS:: NC_000005.10:g.181223837GT[1], NC_000005.10:g.181223837GT[3], NC_000005.9:g.180650837GT[1], NC_000005.9:g.180650837GT[3], NG_030346.1:g.5575GT[1], NG_030346.1:g.5575GT[3], NM_033549.5:c.-163GT[1], NM_033549.5:c.-163GT[3], NM_033549.4:c.-163GT[1], NM_033549.4:c.-163GT[3], NM_201627.3:c.-163GT[1], NM_201627.3:c.-163GT[3], NM_201627.2:c.-163GT[1], NM_201627.2:c.-163GT[3], NR_045218.2:n.557GT[1], NR_045218.2:n.557GT[3], NR_045218.1:n.575GT[1], NR_045218.1:n.575GT[3], XM_006714932.4:c.-163GT[1], XM_006714932.4:c.-163GT[3], XM_006714932.3:c.-163GT[1], XM_006714932.3:c.-163GT[3], XM_006714932.2:c.-163GT[1], XM_006714932.2:c.-163GT[3], XM_006714932.1:c.-163GT[1], XM_006714932.1:c.-163GT[3], XM_006714931.4:c.-163GT[1], XM_006714931.4:c.-163GT[3], XM_006714931.3:c.-163GT[1], XM_006714931.3:c.-163GT[3], XM_006714931.2:c.-163GT[1], XM_006714931.2:c.-163GT[3], XM_006714931.1:c.-163GT[1], XM_006714931.1:c.-163GT[3], XM_006714929.3:c.-163GT[1], XM_006714929.3:c.-163GT[3], XM_006714929.2:c.-163GT[1], XM_006714929.2:c.-163GT[3], XM_006714929.1:c.-163GT[1], XM_006714929.1:c.-163GT[3], XM_006714930.3:c.-163GT[1], XM_006714930.3:c.-163GT[3], XM_006714930.2:c.-163GT[1], XM_006714930.2:c.-163GT[3], XM_006714930.1:c.-163GT[1], XM_006714930.1:c.-163GT[3], XM_047417868.1:c.-163GT[1], XM_047417868.1:c.-163GT[3]

Select item 14910160954.

rs1491016095 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 5:181226871 (GRCh38)
5:180653871 (GRCh37)
Canonical SPDI:: NC_000005.10:181226870:TC:
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000005.10:g.181226871_181226872del, NC_000005.9:g.180653871_180653872del, NG_030346.1:g.8609_8610del

Select item 14910107635.

rs1491010763 has merged into rs34347124 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 5:181228945 (GRCh38)
5:180655945 (GRCh37)
Canonical SPDI:: NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:181228933:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000005.10:g.181228945_181228958del, NC_000005.10:g.181228946_181228958del, NC_000005.10:g.181228947_181228958del, NC_000005.10:g.181228948_181228958del, NC_000005.10:g.181228949_181228958del, NC_000005.10:g.181228950_181228958del, NC_000005.10:g.181228951_181228958del, NC_000005.10:g.181228952_181228958del, NC_000005.10:g.181228953_181228958del, NC_000005.10:g.181228955_181228958del, NC_000005.10:g.181228956_181228958del, NC_000005.10:g.181228957_181228958del, NC_000005.10:g.181228958del, NC_000005.10:g.181228958dup, NC_000005.10:g.181228957_181228958dup, NC_000005.10:g.181228956_181228958dup, NC_000005.10:g.181228955_181228958dup, NC_000005.10:g.181228954_181228958dup, NC_000005.10:g.181228953_181228958dup, NC_000005.10:g.181228952_181228958dup, NC_000005.10:g.181228951_181228958dup, NC_000005.10:g.181228950_181228958dup, NC_000005.10:g.181228949_181228958dup, NC_000005.10:g.181228947_181228958dup, NC_000005.10:g.181228941_181228958dup, NC_000005.10:g.181228938_181228958dup, NC_000005.10:g.181228958_181228959insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000005.10:g.181228958_181228959insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000005.10:g.181228958_181228959insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000005.10:g.181228958_181228959insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000005.9:g.180655945_180655958del, NC_000005.9:g.180655946_180655958del, NC_000005.9:g.180655947_180655958del, NC_000005.9:g.180655948_180655958del, NC_000005.9:g.180655949_180655958del, NC_000005.9:g.180655950_180655958del, NC_000005.9:g.180655951_180655958del, NC_000005.9:g.180655952_180655958del, NC_000005.9:g.180655953_180655958del, NC_000005.9:g.180655955_180655958del, NC_000005.9:g.180655956_180655958del, NC_000005.9:g.180655957_180655958del, NC_000005.9:g.180655958del, NC_000005.9:g.180655958dup, NC_000005.9:g.180655957_180655958dup, NC_000005.9:g.180655956_180655958dup, NC_000005.9:g.180655955_180655958dup, NC_000005.9:g.180655954_180655958dup, NC_000005.9:g.180655953_180655958dup, NC_000005.9:g.180655952_180655958dup, NC_000005.9:g.180655951_180655958dup, NC_000005.9:g.180655950_180655958dup, NC_000005.9:g.180655949_180655958dup, NC_000005.9:g.180655947_180655958dup, NC_000005.9:g.180655941_180655958dup, NC_000005.9:g.180655938_180655958dup, NC_000005.9:g.180655958_180655959insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000005.9:g.180655958_180655959insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000005.9:g.180655958_180655959insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000005.9:g.180655958_180655959insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030346.1:g.10683_10696del, NG_030346.1:g.10684_10696del, NG_030346.1:g.10685_10696del, NG_030346.1:g.10686_10696del, NG_030346.1:g.10687_10696del, NG_030346.1:g.10688_10696del, NG_030346.1:g.10689_10696del, NG_030346.1:g.10690_10696del, NG_030346.1:g.10691_10696del, NG_030346.1:g.10693_10696del, NG_030346.1:g.10694_10696del, NG_030346.1:g.10695_10696del, NG_030346.1:g.10696del, NG_030346.1:g.10696dup, NG_030346.1:g.10695_10696dup, NG_030346.1:g.10694_10696dup, NG_030346.1:g.10693_10696dup, NG_030346.1:g.10692_10696dup, NG_030346.1:g.10691_10696dup, NG_030346.1:g.10690_10696dup, NG_030346.1:g.10689_10696dup, NG_030346.1:g.10688_10696dup, NG_030346.1:g.10687_10696dup, NG_030346.1:g.10685_10696dup, NG_030346.1:g.10679_10696dup, NG_030346.1:g.10676_10696dup, NG_030346.1:g.10696_10697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030346.1:g.10696_10697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030346.1:g.10696_10697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_030346.1:g.10696_10697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14908462406.

rs1490846240 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:181232487 (GRCh38)
5:180659487 (GRCh37)
Canonical SPDI:: NC_000005.10:181232486:A:G
Gene:: TRIM41 (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_000005.10:g.181232487A>G, NC_000005.9:g.180659487A>G, NG_030346.1:g.14225A>G

Select item 14906828277.

rs1490682827 [Homo sapiens]

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

Select item 14905603618.

rs1490560361 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:181227910 (GRCh38)
5:180654910 (GRCh37)
Canonical SPDI:: NC_000005.10:181227909:G:A
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000005.10:g.181227910G>A, NC_000005.9:g.180654910G>A, NG_030346.1:g.9648G>A

Select item 14902312439.

rs1490231243 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 5:181231224 (GRCh38)
5:180658224 (GRCh37)
Canonical SPDI:: NC_000005.10:181231223:G:A,NC_000005.10:181231223:G:C
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000029/4 (GnomAD)
HGVS:: NC_000005.10:g.181231224G>A, NC_000005.10:g.181231224G>C, NC_000005.9:g.180658224G>A, NC_000005.9:g.180658224G>C, NG_030346.1:g.12962G>A, NG_030346.1:g.12962G>C

Select item 149020123810.

rs1490201238 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 5:181229249 (GRCh38)
5:180656249 (GRCh37)
Canonical SPDI:: NC_000005.10:181229248:G:A,NC_000005.10:181229248:G:C
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
C=0.000035/1 (TOMMO)
HGVS:: NC_000005.10:g.181229249G>A, NC_000005.10:g.181229249G>C, NC_000005.9:g.180656249G>A, NC_000005.9:g.180656249G>C, NG_030346.1:g.10987G>A, NG_030346.1:g.10987G>C

Select item 148996530211.

rs1489965302 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 5:181226470 (GRCh38)
5:180653470 (GRCh37)
Canonical SPDI:: NC_000005.10:181226469:G:C
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_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_000005.10:g.181226470G>C, NC_000005.9:g.180653470G>C, NG_030346.1:g.8208G>C

Select item 148968505612.

rs1489685056 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:181232288 (GRCh38)
5:180659288 (GRCh37)
Canonical SPDI:: NC_000005.10:181232287:C:T
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
T=0.000026/7 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000005.10:g.181232288C>T, NC_000005.9:g.180659288C>T, NG_030346.1:g.14026C>T

Select item 148965390013.

rs1489653900 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:181230024 (GRCh38)
5:180657024 (GRCh37)
Canonical SPDI:: NC_000005.10:181230023:A:G
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.181230024A>G, NC_000005.9:g.180657024A>G, NG_030346.1:g.11762A>G

Select item 148952846714.

rs1489528467 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 5:181234431 (GRCh38)
5:180661431 (GRCh37)
Canonical SPDI:: NC_000005.10:181234430:G:T
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
HGVS:: NC_000005.10:g.181234431G>T, NC_000005.9:g.180661431G>T, NG_030346.1:g.16169G>T, NM_033549.5:c.1549G>T, NM_033549.4:c.1549G>T, NP_291027.3:p.Gly517Cys

Select item 148896753415.

rs1488967534 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:181231190 (GRCh38)
5:180658190 (GRCh37)
Canonical SPDI:: NC_000005.10:181231189:A:G
Gene:: TRIM41 (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_000005.10:g.181231190A>G, NC_000005.9:g.180658190A>G, NG_030346.1:g.12928A>G

Select item 148883961316.

rs1488839613 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 5:181228612 (GRCh38)
5:180655612 (GRCh37)
Canonical SPDI:: NC_000005.10:181228611:A:C
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.181228612A>C, NC_000005.9:g.180655612A>C, NG_030346.1:g.10350A>C

Select item 148870716717.

rs1488707167 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 5:181233106 (GRCh38)
5:180660106 (GRCh37)
Canonical SPDI:: NC_000005.10:181233105:T:G
Gene:: TRIM41 (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_000005.10:g.181233106T>G, NC_000005.9:g.180660106T>G, NG_030346.1:g.14844T>G

Select item 148869536018.

rs1488695360 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:181225333 (GRCh38)
5:180652333 (GRCh37)
Canonical SPDI:: NC_000005.10:181225332:C:T
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000036/5 (GnomAD)
HGVS:: NC_000005.10:g.181225333C>T, NC_000005.9:g.180652333C>T, NG_030346.1:g.7071C>T

Select item 148864291619.

rs1488642916 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:181231588 (GRCh38)
5:180658588 (GRCh37)
Canonical SPDI:: NC_000005.10:181231587:C:T
Gene:: TRIM41 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000005.10:g.181231588C>T, NC_000005.9:g.180658588C>T, NG_030346.1:g.13326C>T

Select item 148858394920.

rs1488583949 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTTT>- [Show Flanks]
Chromosome:: 5:181221779 (GRCh38)
5:180648779 (GRCh37)
Canonical SPDI:: NC_000005.10:181221772:TTCTTTCTTT:TTCTTT
Gene:: TRIM41 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTCTTT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000005.10:g.181221775CTTT[1], NC_000005.9:g.180648775CTTT[1], NG_030346.1:g.3513CTTT[1]

<< First< Prev

Page of 239

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 4762

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity