Sequence Name | Change(s) |
---|---|
GRCh38.p7 chr 7 | NC_000007.14:g.14606660A>T |
GRCh37.p13 chr 7 | NC_000007.13:g.14646285A>T |
DGKB RefSeqGene | NG_029494.1:g.239791T>A |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
DGKB transcript variant 1 | NM_004080.2:c. | N/A | Intron Variant |
DGKB transcript variant 2 | NM_145695.2:c. | N/A | Intron Variant |
DGKB transcript variant X2 | XM_005249628.2:c. | N/A | Intron Variant |
DGKB transcript variant X5 | XM_005249629.2:c. | N/A | Intron Variant |
DGKB transcript variant X8 | XM_005249630.2:c. | N/A | Intron Variant |
DGKB transcript variant X15 | XM_005249631.3:c. | N/A | Intron Variant |
DGKB transcript variant X1 | XM_011515153.2:c. | N/A | Intron Variant |
DGKB transcript variant X1 | XM_011515154.2:c. | N/A | Intron Variant |
DGKB transcript variant X10 | XM_011515156.2:c. | N/A | Intron Variant |
DGKB transcript variant X13 | XM_011515157.2:c. | N/A | Intron Variant |
DGKB transcript variant X16 | XM_011515158.2:c. | N/A | Intron Variant |
DGKB transcript variant X4 | XM_017011783.1:c. | N/A | Intron Variant |
DGKB transcript variant X6 | XM_017011784.1:c. | N/A | Intron Variant |
DGKB transcript variant X7 | XM_017011785.1:c. | N/A | Intron Variant |
DGKB transcript variant X9 | XM_017011786.1:c. | N/A | Intron Variant |
DGKB transcript variant X11 | XM_017011787.1:c. | N/A | Intron Variant |
DGKB transcript variant X12 | XM_017011788.1:c. | N/A | Intron Variant |
DGKB transcript variant X14 | XM_017011789.1:c. | N/A | Intron Variant |
DGKB transcript variant X2 | XM_017011790.1:c. | N/A | Intron Variant |
DGKB transcript variant X3 | XM_017011791.1:c. | N/A | Intron Variant |
DGKB transcript variant X19 | XM_017011792.1:c. | N/A | Intron Variant |
DGKB transcript variant X5 | XR_001744571.1:n. | N/A | Intron Variant |
There is no significant Hi-C chromatin interaction data for this SNP.