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Select item 14914537731.

rs1491453773 has merged into rs33946641 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:161092774 (GRCh38)
3:160810562 (GRCh37)
Canonical SPDI:: NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
-=0.000238/63 (TOPMED)
HGVS:: NC_000003.12:g.161092774_161092784del, NC_000003.12:g.161092775_161092784del, NC_000003.12:g.161092776_161092784del, NC_000003.12:g.161092777_161092784del, NC_000003.12:g.161092778_161092784del, NC_000003.12:g.161092779_161092784del, NC_000003.12:g.161092780_161092784del, NC_000003.12:g.161092781_161092784del, NC_000003.12:g.161092782_161092784del, NC_000003.12:g.161092783_161092784del, NC_000003.12:g.161092784del, NC_000003.12:g.161092784dup, NC_000003.12:g.161092783_161092784dup, NC_000003.12:g.161092782_161092784dup, NC_000003.12:g.161092781_161092784dup, NC_000003.12:g.161092780_161092784dup, NC_000003.12:g.161092779_161092784dup, NC_000003.12:g.161092778_161092784dup, NC_000003.12:g.161092777_161092784dup, NC_000003.12:g.161092776_161092784dup, NC_000003.12:g.161092775_161092784dup, NC_000003.12:g.161092774_161092784dup, NC_000003.12:g.161092773_161092784dup, NC_000003.12:g.161092772_161092784dup, NC_000003.12:g.161092771_161092784dup, NC_000003.12:g.161092769_161092784dup, NC_000003.12:g.161092784_161092785insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.161092784_161092785insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.161092784_161092785insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.160810562_160810572del, NC_000003.11:g.160810563_160810572del, NC_000003.11:g.160810564_160810572del, NC_000003.11:g.160810565_160810572del, NC_000003.11:g.160810566_160810572del, NC_000003.11:g.160810567_160810572del, NC_000003.11:g.160810568_160810572del, NC_000003.11:g.160810569_160810572del, NC_000003.11:g.160810570_160810572del, NC_000003.11:g.160810571_160810572del, NC_000003.11:g.160810572del, NC_000003.11:g.160810572dup, NC_000003.11:g.160810571_160810572dup, NC_000003.11:g.160810570_160810572dup, NC_000003.11:g.160810569_160810572dup, NC_000003.11:g.160810568_160810572dup, NC_000003.11:g.160810567_160810572dup, NC_000003.11:g.160810566_160810572dup, NC_000003.11:g.160810565_160810572dup, NC_000003.11:g.160810564_160810572dup, NC_000003.11:g.160810563_160810572dup, NC_000003.11:g.160810562_160810572dup, NC_000003.11:g.160810561_160810572dup, NC_000003.11:g.160810560_160810572dup, NC_000003.11:g.160810559_160810572dup, NC_000003.11:g.160810557_160810572dup, NC_000003.11:g.160810572_160810573insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.160810572_160810573insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.160810572_160810573insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_007854.1:g.17599_17609del, NG_007854.1:g.17600_17609del, NG_007854.1:g.17601_17609del, NG_007854.1:g.17602_17609del, NG_007854.1:g.17603_17609del, NG_007854.1:g.17604_17609del, NG_007854.1:g.17605_17609del, NG_007854.1:g.17606_17609del, NG_007854.1:g.17607_17609del, NG_007854.1:g.17608_17609del, NG_007854.1:g.17609del, NG_007854.1:g.17609dup, NG_007854.1:g.17608_17609dup, NG_007854.1:g.17607_17609dup, NG_007854.1:g.17606_17609dup, NG_007854.1:g.17605_17609dup, NG_007854.1:g.17604_17609dup, NG_007854.1:g.17603_17609dup, NG_007854.1:g.17602_17609dup, NG_007854.1:g.17601_17609dup, NG_007854.1:g.17600_17609dup, NG_007854.1:g.17599_17609dup, NG_007854.1:g.17598_17609dup, NG_007854.1:g.17597_17609dup, NG_007854.1:g.17596_17609dup, NG_007854.1:g.17594_17609dup, NG_007854.1:g.17609_17610insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_007854.1:g.17609_17610insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_007854.1:g.17609_17610insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14913302302.

rs1491330230 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTT [Show Flanks]
Chromosome:: 3:161092764 (GRCh38)
3:160810553 (GRCh37)
Canonical SPDI:: NC_000003.12:161092764:TT:TTCTT
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTCTT=0.00008/1 (ALFA)
TTC=0.00036/19 (GnomAD)
HGVS:: NC_000003.12:g.161092766_161092767insCTT, NC_000003.11:g.160810554_160810555insCTT, NG_007854.1:g.17608_17609insGAA

Select item 14909747913.

rs1490974791 has merged into rs33946641 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:161092774 (GRCh38)
3:160810562 (GRCh37)
Canonical SPDI:: NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:161092763:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
-=0.000238/63 (TOPMED)
HGVS:: NC_000003.12:g.161092774_161092784del, NC_000003.12:g.161092775_161092784del, NC_000003.12:g.161092776_161092784del, NC_000003.12:g.161092777_161092784del, NC_000003.12:g.161092778_161092784del, NC_000003.12:g.161092779_161092784del, NC_000003.12:g.161092780_161092784del, NC_000003.12:g.161092781_161092784del, NC_000003.12:g.161092782_161092784del, NC_000003.12:g.161092783_161092784del, NC_000003.12:g.161092784del, NC_000003.12:g.161092784dup, NC_000003.12:g.161092783_161092784dup, NC_000003.12:g.161092782_161092784dup, NC_000003.12:g.161092781_161092784dup, NC_000003.12:g.161092780_161092784dup, NC_000003.12:g.161092779_161092784dup, NC_000003.12:g.161092778_161092784dup, NC_000003.12:g.161092777_161092784dup, NC_000003.12:g.161092776_161092784dup, NC_000003.12:g.161092775_161092784dup, NC_000003.12:g.161092774_161092784dup, NC_000003.12:g.161092773_161092784dup, NC_000003.12:g.161092772_161092784dup, NC_000003.12:g.161092771_161092784dup, NC_000003.12:g.161092769_161092784dup, NC_000003.12:g.161092784_161092785insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.161092784_161092785insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.161092784_161092785insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.160810562_160810572del, NC_000003.11:g.160810563_160810572del, NC_000003.11:g.160810564_160810572del, NC_000003.11:g.160810565_160810572del, NC_000003.11:g.160810566_160810572del, NC_000003.11:g.160810567_160810572del, NC_000003.11:g.160810568_160810572del, NC_000003.11:g.160810569_160810572del, NC_000003.11:g.160810570_160810572del, NC_000003.11:g.160810571_160810572del, NC_000003.11:g.160810572del, NC_000003.11:g.160810572dup, NC_000003.11:g.160810571_160810572dup, NC_000003.11:g.160810570_160810572dup, NC_000003.11:g.160810569_160810572dup, NC_000003.11:g.160810568_160810572dup, NC_000003.11:g.160810567_160810572dup, NC_000003.11:g.160810566_160810572dup, NC_000003.11:g.160810565_160810572dup, NC_000003.11:g.160810564_160810572dup, NC_000003.11:g.160810563_160810572dup, NC_000003.11:g.160810562_160810572dup, NC_000003.11:g.160810561_160810572dup, NC_000003.11:g.160810560_160810572dup, NC_000003.11:g.160810559_160810572dup, NC_000003.11:g.160810557_160810572dup, NC_000003.11:g.160810572_160810573insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.160810572_160810573insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.160810572_160810573insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_007854.1:g.17599_17609del, NG_007854.1:g.17600_17609del, NG_007854.1:g.17601_17609del, NG_007854.1:g.17602_17609del, NG_007854.1:g.17603_17609del, NG_007854.1:g.17604_17609del, NG_007854.1:g.17605_17609del, NG_007854.1:g.17606_17609del, NG_007854.1:g.17607_17609del, NG_007854.1:g.17608_17609del, NG_007854.1:g.17609del, NG_007854.1:g.17609dup, NG_007854.1:g.17608_17609dup, NG_007854.1:g.17607_17609dup, NG_007854.1:g.17606_17609dup, NG_007854.1:g.17605_17609dup, NG_007854.1:g.17604_17609dup, NG_007854.1:g.17603_17609dup, NG_007854.1:g.17602_17609dup, NG_007854.1:g.17601_17609dup, NG_007854.1:g.17600_17609dup, NG_007854.1:g.17599_17609dup, NG_007854.1:g.17598_17609dup, NG_007854.1:g.17597_17609dup, NG_007854.1:g.17596_17609dup, NG_007854.1:g.17594_17609dup, NG_007854.1:g.17609_17610insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_007854.1:g.17609_17610insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_007854.1:g.17609_17610insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14909244384.

rs1490924438 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:161091907 (GRCh38)
3:160809695 (GRCh37)
Canonical SPDI:: NC_000003.12:161091906:G:A
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.161091907G>A, NC_000003.11:g.160809695G>A, NG_007854.1:g.18466C>T

Select item 14906900755.

rs1490690075 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:161106975 (GRCh38)
3:160824763 (GRCh37)
Canonical SPDI:: NC_000003.12:161106974:A:G
Gene:: B3GALNT1 (Varview), LOC124909453 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_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_000003.12:g.161106975A>G, NC_000003.11:g.160824763A>G, NG_007854.1:g.3398T>C, XR_007096146.1:n.617A>G, XR_007096147.1:n.610A>G

Select item 14904080276.

rs1490408027 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 3:161099470 (GRCh38)
3:160817258 (GRCh37)
Canonical SPDI:: NC_000003.12:161099469:C:G,NC_000003.12:161099469:C:T
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.161099470C>G, NC_000003.12:g.161099470C>T, NC_000003.11:g.160817258C>G, NC_000003.11:g.160817258C>T, NG_007854.1:g.10903G>C, NG_007854.1:g.10903G>A

Select item 14900525937.

rs1490052593 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 3:161084965 (GRCh38)
3:160802753 (GRCh37)
Canonical SPDI:: NC_000003.12:161084964:T:G
Gene:: B3GALNT1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.161084965T>G, NC_000003.11:g.160802753T>G, NG_007854.1:g.25408A>C, NM_003781.4:c.*794A>C, NM_003781.3:c.*794A>C, NM_033169.3:c.*794A>C, NM_033169.2:c.*794A>C, NM_033167.3:c.*794A>C, NM_033167.2:c.*794A>C, NM_033168.3:c.*794A>C, NM_033168.2:c.*794A>C, NM_001349145.2:c.*794A>C, NM_001349145.1:c.*794A>C, NM_001349147.2:c.*794A>C, NM_001349147.1:c.*794A>C, NM_001349159.2:c.*794A>C, NM_001349159.1:c.*794A>C, NM_001349150.2:c.*794A>C, NM_001349150.1:c.*794A>C, NM_001349149.2:c.*794A>C, NM_001349149.1:c.*794A>C, NM_001349162.2:c.*794A>C, NM_001349162.1:c.*794A>C, NM_001349156.2:c.*794A>C, NM_001349156.1:c.*794A>C, NM_001349155.2:c.*794A>C, NM_001349155.1:c.*794A>C, NM_001349152.2:c.*794A>C, NM_001349152.1:c.*794A>C, NM_001349157.2:c.*794A>C, NM_001349157.1:c.*794A>C, NM_001349146.2:c.*794A>C, NM_001349146.1:c.*794A>C, NM_001349154.2:c.*794A>C, NM_001349154.1:c.*794A>C, NM_001349158.2:c.*794A>C, NM_001349158.1:c.*794A>C, NM_001349143.2:c.*794A>C, NM_001349143.1:c.*794A>C, NM_001349151.2:c.*794A>C, NM_001349151.1:c.*794A>C, NM_001349131.2:c.*794A>C, NM_001349131.1:c.*794A>C, NM_001038628.2:c.*794A>C, NM_001038628.1:c.*794A>C, NM_001349139.2:c.*794A>C, NM_001349139.1:c.*794A>C, NM_001349130.2:c.*794A>C, NM_001349130.1:c.*794A>C, NM_001349148.2:c.*794A>C, NM_001349148.1:c.*794A>C, NM_001349137.2:c.*794A>C, NM_001349137.1:c.*794A>C, NM_001349153.2:c.*794A>C, NM_001349153.1:c.*794A>C, NM_001349140.2:c.*794A>C, NM_001349140.1:c.*794A>C, NM_001349132.2:c.*794A>C, NM_001349132.1:c.*794A>C, NM_001349144.2:c.*794A>C, NM_001349144.1:c.*794A>C, NM_001349163.2:c.*794A>C, NM_001349163.1:c.*794A>C, NM_001349138.2:c.*794A>C, NM_001349138.1:c.*794A>C, NM_001349161.2:c.*794A>C, NM_001349161.1:c.*794A>C, NM_001349133.2:c.*794A>C, NM_001349133.1:c.*794A>C, NM_001349135.2:c.*794A>C, NM_001349135.1:c.*794A>C, NM_001349141.2:c.*794A>C, NM_001349141.1:c.*794A>C, NM_001349136.2:c.*794A>C, NM_001349136.1:c.*794A>C, NM_001349134.2:c.*794A>C, NM_001349134.1:c.*794A>C, NM_001349142.2:c.*794A>C, NM_001349142.1:c.*794A>C, NM_001349160.1:c.*794A>C, XM_005247859.6:c.*794A>C, XM_005247859.5:c.*794A>C, XM_005247859.4:c.*794A>C, XM_005247859.3:c.*794A>C, XM_005247859.2:c.*794A>C, XM_005247859.1:c.*794A>C, XM_047449132.1:c.*794A>C, XM_047449133.1:c.*794A>C, XM_047449131.1:c.*794A>C, XM_047449136.1:c.*794A>C, XM_047449138.1:c.*794A>C, XM_047449137.1:c.*794A>C, XM_047449135.1:c.*794A>C, XM_024453808.1:c.*794A>C

Select item 14898858248.

rs1489885824 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:161084533 (GRCh38)
3:160802321 (GRCh37)
Canonical SPDI:: NC_000003.12:161084532:G:A
Gene:: B3GALNT1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.161084533G>A, NC_000003.11:g.160802321G>A, NG_007854.1:g.25840C>T, NM_003781.4:c.*1226C>T, NM_003781.3:c.*1226C>T, NM_033169.3:c.*1226C>T, NM_033169.2:c.*1226C>T, NM_033167.3:c.*1226C>T, NM_033167.2:c.*1226C>T, NM_033168.3:c.*1226C>T, NM_033168.2:c.*1226C>T, NM_001349145.2:c.*1226C>T, NM_001349145.1:c.*1226C>T, NM_001349147.2:c.*1226C>T, NM_001349147.1:c.*1226C>T, NM_001349159.2:c.*1226C>T, NM_001349159.1:c.*1226C>T, NM_001349150.2:c.*1226C>T, NM_001349150.1:c.*1226C>T, NM_001349149.2:c.*1226C>T, NM_001349149.1:c.*1226C>T, NM_001349162.2:c.*1226C>T, NM_001349162.1:c.*1226C>T, NM_001349156.2:c.*1226C>T, NM_001349156.1:c.*1226C>T, NM_001349155.2:c.*1226C>T, NM_001349155.1:c.*1226C>T, NM_001349152.2:c.*1226C>T, NM_001349152.1:c.*1226C>T, NM_001349157.2:c.*1226C>T, NM_001349157.1:c.*1226C>T, NM_001349146.2:c.*1226C>T, NM_001349146.1:c.*1226C>T, NM_001349154.2:c.*1226C>T, NM_001349154.1:c.*1226C>T, NM_001349158.2:c.*1226C>T, NM_001349158.1:c.*1226C>T, NM_001349143.2:c.*1226C>T, NM_001349143.1:c.*1226C>T, NM_001349151.2:c.*1226C>T, NM_001349151.1:c.*1226C>T, NM_001349131.2:c.*1226C>T, NM_001349131.1:c.*1226C>T, NM_001038628.2:c.*1226C>T, NM_001038628.1:c.*1226C>T, NM_001349139.2:c.*1226C>T, NM_001349139.1:c.*1226C>T, NM_001349130.2:c.*1226C>T, NM_001349130.1:c.*1226C>T, NM_001349148.2:c.*1226C>T, NM_001349148.1:c.*1226C>T, NM_001349137.2:c.*1226C>T, NM_001349137.1:c.*1226C>T, NM_001349153.2:c.*1226C>T, NM_001349153.1:c.*1226C>T, NM_001349140.2:c.*1226C>T, NM_001349140.1:c.*1226C>T, NM_001349132.2:c.*1226C>T, NM_001349132.1:c.*1226C>T, NM_001349144.2:c.*1226C>T, NM_001349144.1:c.*1226C>T, NM_001349163.2:c.*1226C>T, NM_001349163.1:c.*1226C>T, NM_001349138.2:c.*1226C>T, NM_001349138.1:c.*1226C>T, NM_001349161.2:c.*1226C>T, NM_001349161.1:c.*1226C>T, NM_001349133.2:c.*1226C>T, NM_001349133.1:c.*1226C>T, NM_001349135.2:c.*1226C>T, NM_001349135.1:c.*1226C>T, NM_001349141.2:c.*1226C>T, NM_001349141.1:c.*1226C>T, NM_001349136.2:c.*1226C>T, NM_001349136.1:c.*1226C>T, NM_001349134.2:c.*1226C>T, NM_001349134.1:c.*1226C>T, NM_001349142.2:c.*1226C>T, NM_001349142.1:c.*1226C>T, NM_001349160.1:c.*1226C>T, XM_005247859.6:c.*1226C>T, XM_005247859.5:c.*1226C>T, XM_005247859.4:c.*1226C>T, XM_005247859.3:c.*1226C>T, XM_005247859.2:c.*1226C>T, XM_005247859.1:c.*1226C>T, XM_047449132.1:c.*1226C>T, XM_047449133.1:c.*1226C>T, XM_047449131.1:c.*1226C>T, XM_047449136.1:c.*1226C>T, XM_047449138.1:c.*1226C>T, XM_047449137.1:c.*1226C>T, XM_047449135.1:c.*1226C>T, XM_024453808.1:c.*1226C>T

Select item 14898311409.

rs1489831140 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:161093003 (GRCh38)
3:160810791 (GRCh37)
Canonical SPDI:: NC_000003.12:161093002:C:T
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000026/7 (TOPMED)
T=0.001092/2 (Korea1K)
HGVS:: NC_000003.12:g.161093003C>T, NC_000003.11:g.160810791C>T, NG_007854.1:g.17370G>A

Select item 148976505410.

rs1489765054 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 3:161092402 (GRCh38)
3:160810190 (GRCh37)
Canonical SPDI:: NC_000003.12:161092401:G:C
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000003.12:g.161092402G>C, NC_000003.11:g.160810190G>C, NG_007854.1:g.17971C>G

Select item 148935231511.

rs1489352315 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:161095688 (GRCh38)
3:160813476 (GRCh37)
Canonical SPDI:: NC_000003.12:161095687:T:C
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_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_000003.12:g.161095688T>C, NC_000003.11:g.160813476T>C, NG_007854.1:g.14685A>G

Select item 148932806812.

rs1489328068 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:161085435 (GRCh38)
3:160803223 (GRCh37)
Canonical SPDI:: NC_000003.12:161085434:C:T
Gene:: B3GALNT1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.161085435C>T, NC_000003.11:g.160803223C>T, NG_007854.1:g.24938G>A, NM_003781.4:c.*324G>A, NM_003781.3:c.*324G>A, NM_033169.3:c.*324G>A, NM_033169.2:c.*324G>A, NM_033167.3:c.*324G>A, NM_033167.2:c.*324G>A, NM_033168.3:c.*324G>A, NM_033168.2:c.*324G>A, NM_001349145.2:c.*324G>A, NM_001349145.1:c.*324G>A, NM_001349147.2:c.*324G>A, NM_001349147.1:c.*324G>A, NM_001349159.2:c.*324G>A, NM_001349159.1:c.*324G>A, NM_001349150.2:c.*324G>A, NM_001349150.1:c.*324G>A, NM_001349149.2:c.*324G>A, NM_001349149.1:c.*324G>A, NM_001349162.2:c.*324G>A, NM_001349162.1:c.*324G>A, NM_001349156.2:c.*324G>A, NM_001349156.1:c.*324G>A, NM_001349155.2:c.*324G>A, NM_001349155.1:c.*324G>A, NM_001349152.2:c.*324G>A, NM_001349152.1:c.*324G>A, NM_001349157.2:c.*324G>A, NM_001349157.1:c.*324G>A, NM_001349146.2:c.*324G>A, NM_001349146.1:c.*324G>A, NM_001349154.2:c.*324G>A, NM_001349154.1:c.*324G>A, NM_001349158.2:c.*324G>A, NM_001349158.1:c.*324G>A, NM_001349143.2:c.*324G>A, NM_001349143.1:c.*324G>A, NM_001349151.2:c.*324G>A, NM_001349151.1:c.*324G>A, NM_001349131.2:c.*324G>A, NM_001349131.1:c.*324G>A, NM_001038628.2:c.*324G>A, NM_001038628.1:c.*324G>A, NM_001349139.2:c.*324G>A, NM_001349139.1:c.*324G>A, NM_001349130.2:c.*324G>A, NM_001349130.1:c.*324G>A, NM_001349148.2:c.*324G>A, NM_001349148.1:c.*324G>A, NM_001349137.2:c.*324G>A, NM_001349137.1:c.*324G>A, NM_001349153.2:c.*324G>A, NM_001349153.1:c.*324G>A, NM_001349140.2:c.*324G>A, NM_001349140.1:c.*324G>A, NM_001349132.2:c.*324G>A, NM_001349132.1:c.*324G>A, NM_001349144.2:c.*324G>A, NM_001349144.1:c.*324G>A, NM_001349163.2:c.*324G>A, NM_001349163.1:c.*324G>A, NM_001349138.2:c.*324G>A, NM_001349138.1:c.*324G>A, NM_001349161.2:c.*324G>A, NM_001349161.1:c.*324G>A, NM_001349133.2:c.*324G>A, NM_001349133.1:c.*324G>A, NM_001349135.2:c.*324G>A, NM_001349135.1:c.*324G>A, NM_001349141.2:c.*324G>A, NM_001349141.1:c.*324G>A, NM_001349136.2:c.*324G>A, NM_001349136.1:c.*324G>A, NM_001349134.2:c.*324G>A, NM_001349134.1:c.*324G>A, NM_001349142.2:c.*324G>A, NM_001349142.1:c.*324G>A, NM_001349160.1:c.*324G>A, XM_005247859.6:c.*324G>A, XM_005247859.5:c.*324G>A, XM_005247859.4:c.*324G>A, XM_005247859.3:c.*324G>A, XM_005247859.2:c.*324G>A, XM_005247859.1:c.*324G>A, XM_047449132.1:c.*324G>A, XM_047449133.1:c.*324G>A, XM_047449131.1:c.*324G>A, XM_047449136.1:c.*324G>A, XM_047449138.1:c.*324G>A, XM_047449137.1:c.*324G>A, XM_047449135.1:c.*324G>A, XM_024453808.1:c.*324G>A

Select item 148932292113.

rs1489322921 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:161093152 (GRCh38)
3:160810940 (GRCh37)
Canonical SPDI:: NC_000003.12:161093151:C:T
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.161093152C>T, NC_000003.11:g.160810940C>T, NG_007854.1:g.17221G>A

Select item 148922731914.

rs1489227319 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 3:161102564 (GRCh38)
3:160820352 (GRCh37)
Canonical SPDI:: NC_000003.12:161102563:TTTTTT:TTTTT
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTTT=0.000071/1 (ALFA)
-=0.000014/2 (GnomAD)
HGVS:: NC_000003.12:g.161102569del, NC_000003.11:g.160820357del, NG_007854.1:g.7809del

Select item 148888917715.

rs1488889177 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:161094279 (GRCh38)
3:160812067 (GRCh37)
Canonical SPDI:: NC_000003.12:161094278:T:C
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.161094279T>C, NC_000003.11:g.160812067T>C, NG_007854.1:g.16094A>G

Select item 148887749816.

rs1488877498 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:161093502 (GRCh38)
3:160811290 (GRCh37)
Canonical SPDI:: NC_000003.12:161093501:G:A
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000003.12:g.161093502G>A, NC_000003.11:g.160811290G>A, NG_007854.1:g.16871C>T

Select item 148881828417.

rs1488818284 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 3:161093086 (GRCh38)
3:160810874 (GRCh37)
Canonical SPDI:: NC_000003.12:161093085:G:C
Gene:: B3GALNT1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.161093086G>C, NC_000003.11:g.160810874G>C, NG_007854.1:g.17287C>G

Select item 148856310318.

rs1488563103 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:161085074 (GRCh38)
3:160802862 (GRCh37)
Canonical SPDI:: NC_000003.12:161085073:T:C
Gene:: B3GALNT1 (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_000003.12:g.161085074T>C, NC_000003.11:g.160802862T>C, NG_007854.1:g.25299A>G, NM_003781.4:c.*685A>G, NM_003781.3:c.*685A>G, NM_033169.3:c.*685A>G, NM_033169.2:c.*685A>G, NM_033167.3:c.*685A>G, NM_033167.2:c.*685A>G, NM_033168.3:c.*685A>G, NM_033168.2:c.*685A>G, NM_001349145.2:c.*685A>G, NM_001349145.1:c.*685A>G, NM_001349147.2:c.*685A>G, NM_001349147.1:c.*685A>G, NM_001349159.2:c.*685A>G, NM_001349159.1:c.*685A>G, NM_001349150.2:c.*685A>G, NM_001349150.1:c.*685A>G, NM_001349149.2:c.*685A>G, NM_001349149.1:c.*685A>G, NM_001349162.2:c.*685A>G, NM_001349162.1:c.*685A>G, NM_001349156.2:c.*685A>G, NM_001349156.1:c.*685A>G, NM_001349155.2:c.*685A>G, NM_001349155.1:c.*685A>G, NM_001349152.2:c.*685A>G, NM_001349152.1:c.*685A>G, NM_001349157.2:c.*685A>G, NM_001349157.1:c.*685A>G, NM_001349146.2:c.*685A>G, NM_001349146.1:c.*685A>G, NM_001349154.2:c.*685A>G, NM_001349154.1:c.*685A>G, NM_001349158.2:c.*685A>G, NM_001349158.1:c.*685A>G, NM_001349143.2:c.*685A>G, NM_001349143.1:c.*685A>G, NM_001349151.2:c.*685A>G, NM_001349151.1:c.*685A>G, NM_001349131.2:c.*685A>G, NM_001349131.1:c.*685A>G, NM_001038628.2:c.*685A>G, NM_001038628.1:c.*685A>G, NM_001349139.2:c.*685A>G, NM_001349139.1:c.*685A>G, NM_001349130.2:c.*685A>G, NM_001349130.1:c.*685A>G, NM_001349148.2:c.*685A>G, NM_001349148.1:c.*685A>G, NM_001349137.2:c.*685A>G, NM_001349137.1:c.*685A>G, NM_001349153.2:c.*685A>G, NM_001349153.1:c.*685A>G, NM_001349140.2:c.*685A>G, NM_001349140.1:c.*685A>G, NM_001349132.2:c.*685A>G, NM_001349132.1:c.*685A>G, NM_001349144.2:c.*685A>G, NM_001349144.1:c.*685A>G, NM_001349163.2:c.*685A>G, NM_001349163.1:c.*685A>G, NM_001349138.2:c.*685A>G, NM_001349138.1:c.*685A>G, NM_001349161.2:c.*685A>G, NM_001349161.1:c.*685A>G, NM_001349133.2:c.*685A>G, NM_001349133.1:c.*685A>G, NM_001349135.2:c.*685A>G, NM_001349135.1:c.*685A>G, NM_001349141.2:c.*685A>G, NM_001349141.1:c.*685A>G, NM_001349136.2:c.*685A>G, NM_001349136.1:c.*685A>G, NM_001349134.2:c.*685A>G, NM_001349134.1:c.*685A>G, NM_001349142.2:c.*685A>G, NM_001349142.1:c.*685A>G, NM_001349160.1:c.*685A>G, XM_005247859.6:c.*685A>G, XM_005247859.5:c.*685A>G, XM_005247859.4:c.*685A>G, XM_005247859.3:c.*685A>G, XM_005247859.2:c.*685A>G, XM_005247859.1:c.*685A>G, XM_047449132.1:c.*685A>G, XM_047449133.1:c.*685A>G, XM_047449131.1:c.*685A>G, XM_047449136.1:c.*685A>G, XM_047449138.1:c.*685A>G, XM_047449137.1:c.*685A>G, XM_047449135.1:c.*685A>G, XM_024453808.1:c.*685A>G

Select item 148842897819.

rs1488428978 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 3:161085497 (GRCh38)
3:160803285 (GRCh37)
Canonical SPDI:: NC_000003.12:161085496:T:A
Gene:: B3GALNT1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000076/20 (TOPMED)
HGVS:: NC_000003.12:g.161085497T>A, NC_000003.11:g.160803285T>A, NG_007854.1:g.24876A>T, NM_003781.4:c.*262A>T, NM_003781.3:c.*262A>T, NM_033169.3:c.*262A>T, NM_033169.2:c.*262A>T, NM_033167.3:c.*262A>T, NM_033167.2:c.*262A>T, NM_033168.3:c.*262A>T, NM_033168.2:c.*262A>T, NM_001349145.2:c.*262A>T, NM_001349145.1:c.*262A>T, NM_001349147.2:c.*262A>T, NM_001349147.1:c.*262A>T, NM_001349159.2:c.*262A>T, NM_001349159.1:c.*262A>T, NM_001349150.2:c.*262A>T, NM_001349150.1:c.*262A>T, NM_001349149.2:c.*262A>T, NM_001349149.1:c.*262A>T, NM_001349162.2:c.*262A>T, NM_001349162.1:c.*262A>T, NM_001349156.2:c.*262A>T, NM_001349156.1:c.*262A>T, NM_001349155.2:c.*262A>T, NM_001349155.1:c.*262A>T, NM_001349152.2:c.*262A>T, NM_001349152.1:c.*262A>T, NM_001349157.2:c.*262A>T, NM_001349157.1:c.*262A>T, NM_001349146.2:c.*262A>T, NM_001349146.1:c.*262A>T, NM_001349154.2:c.*262A>T, NM_001349154.1:c.*262A>T, NM_001349158.2:c.*262A>T, NM_001349158.1:c.*262A>T, NM_001349143.2:c.*262A>T, NM_001349143.1:c.*262A>T, NM_001349151.2:c.*262A>T, NM_001349151.1:c.*262A>T, NM_001349131.2:c.*262A>T, NM_001349131.1:c.*262A>T, NM_001038628.2:c.*262A>T, NM_001038628.1:c.*262A>T, NM_001349139.2:c.*262A>T, NM_001349139.1:c.*262A>T, NM_001349130.2:c.*262A>T, NM_001349130.1:c.*262A>T, NM_001349148.2:c.*262A>T, NM_001349148.1:c.*262A>T, NM_001349137.2:c.*262A>T, NM_001349137.1:c.*262A>T, NM_001349153.2:c.*262A>T, NM_001349153.1:c.*262A>T, NM_001349140.2:c.*262A>T, NM_001349140.1:c.*262A>T, NM_001349132.2:c.*262A>T, NM_001349132.1:c.*262A>T, NM_001349144.2:c.*262A>T, NM_001349144.1:c.*262A>T, NM_001349163.2:c.*262A>T, NM_001349163.1:c.*262A>T, NM_001349138.2:c.*262A>T, NM_001349138.1:c.*262A>T, NM_001349161.2:c.*262A>T, NM_001349161.1:c.*262A>T, NM_001349133.2:c.*262A>T, NM_001349133.1:c.*262A>T, NM_001349135.2:c.*262A>T, NM_001349135.1:c.*262A>T, NM_001349141.2:c.*262A>T, NM_001349141.1:c.*262A>T, NM_001349136.2:c.*262A>T, NM_001349136.1:c.*262A>T, NM_001349134.2:c.*262A>T, NM_001349134.1:c.*262A>T, NM_001349142.2:c.*262A>T, NM_001349142.1:c.*262A>T, NM_001349160.1:c.*262A>T, XM_005247859.6:c.*262A>T, XM_005247859.5:c.*262A>T, XM_005247859.4:c.*262A>T, XM_005247859.3:c.*262A>T, XM_005247859.2:c.*262A>T, XM_005247859.1:c.*262A>T, XM_047449132.1:c.*262A>T, XM_047449133.1:c.*262A>T, XM_047449131.1:c.*262A>T, XM_047449136.1:c.*262A>T, XM_047449138.1:c.*262A>T, XM_047449137.1:c.*262A>T, XM_047449135.1:c.*262A>T, XM_024453808.1:c.*262A>T

Select item 148834272620.

rs1488342726 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:161106898 (GRCh38)
3:160824686 (GRCh37)
Canonical SPDI:: NC_000003.12:161106897:G:A
Gene:: B3GALNT1 (Varview), LOC124909453 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
HGVS:: NC_000003.12:g.161106898G>A, NC_000003.11:g.160824686G>A, NG_007854.1:g.3475C>T, XR_007096146.1:n.540G>A, XR_007096147.1:n.533G>A

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