Table 4. Position of intronic variations... | American Society of Hematology

Table 4.

Position of intronic variations and their reference SNP number detected in all samples sequenced

Position	hg38 (RHD*DAU0)	All samples	Location	Reference SNP no.*
25 277 761	A	G	Intron 1	rs28661958
25 286 520	T	C	Intron 2	rs183024534
25 286 601	T	A	Intron 2	NA†
25 286 605	A	T	Intron 2	NA†
25 286 674	C	T	Intron 2	NA†
25 286 732	A	G	Intron 2	NA†
25 290 908	T	C	Intron 3	rs28521909
25 290 915	G	A	Intron 3	rs28562109
25 295 850	A	G	Intron 3	rs28451966
25 297 140	G	A	Intron 3	rs28786680
25 305 164	G	T	Intron 6	rs28703207
25 308 306	T	C	Intron 7	rs28374144
25 308 317	T	C	Intron 7	rs28719684
25 308 325	G	A	Intron 7	rs71493569
25 308 326	C	T	Intron 7	rs71493569
25 308 403	C	T	Intron 7	rs1801096
25 316 058	A	G	Intron 7	rs28453868
25 319 292	T	C	Intron 8	rs28397158
25 322 588	A	G	Intron 9	rs28435180
25 327 036	G	A	Intron 9	rs61777612
25 329 789	A	G	Intron 10	rs28654325

Position	hg38 (RHD*DAU0)	All samples	Location	Reference SNP no.*
25 277 761	A	G	Intron 1	rs28661958
25 286 520	T	C	Intron 2	rs183024534
25 286 601	T	A	Intron 2	NA†
25 286 605	A	T	Intron 2	NA†
25 286 674	C	T	Intron 2	NA†
25 286 732	A	G	Intron 2	NA†
25 290 908	T	C	Intron 3	rs28521909
25 290 915	G	A	Intron 3	rs28562109
25 295 850	A	G	Intron 3	rs28451966
25 297 140	G	A	Intron 3	rs28786680
25 305 164	G	T	Intron 6	rs28703207
25 308 306	T	C	Intron 7	rs28374144
25 308 317	T	C	Intron 7	rs28719684
25 308 325	G	A	Intron 7	rs71493569
25 308 326	C	T	Intron 7	rs71493569
25 308 403	C	T	Intron 7	rs1801096
25 316 058	A	G	Intron 7	rs28453868
25 319 292	T	C	Intron 8	rs28397158
25 322 588	A	G	Intron 9	rs28435180
25 327 036	G	A	Intron 9	rs61777612
25 329 789	A	G	Intron 10	rs28654325

As the reference sequence is RHD*DAU0 (RHD*10.00), these nucleotide changes are predicted to be RHD*DAU0 (RHD*10.00) specific.

From the database of SNPs.⁴⁴

Not applicable. Not found in the database of SNPs.⁴⁴