List of variants in gene DSP reported as likely benign by Color

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 71

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HGVS	dbSNP
NM_004415.4(DSP):c.1005A>G (p.Gln335=)	rs200961741
NM_004415.4(DSP):c.1045-8T>C	rs201633815
NM_004415.4(DSP):c.1206G>A (p.Lys402=)	rs150422458
NM_004415.4(DSP):c.1266+6G>A	rs73375345
NM_004415.4(DSP):c.1329G>A (p.Lys443=)	rs767785995
NM_004415.4(DSP):c.1344G>A (p.Leu448=)	rs138226280
NM_004415.4(DSP):c.1483G>A (p.Val495Met)	rs372014020
NM_004415.4(DSP):c.1488G>A (p.Thr496=)	rs35820473
NM_004415.4(DSP):c.1695C>T (p.Ile565=)	rs752714010
NM_004415.4(DSP):c.2121C>T (p.Asn707=)	rs368590198
NM_004415.4(DSP):c.2205T>C (p.Gly735=)	rs1561692450
NM_004415.4(DSP):c.2346C>T (p.Asp782=)	rs139071827
NM_004415.4(DSP):c.2422C>T (p.Arg808Cys)	rs150339369
NM_004415.4(DSP):c.2568C>T (p.Phe856=)	rs746036365
NM_004415.4(DSP):c.2723G>A (p.Arg908His)	rs142494121
NM_004415.4(DSP):c.2773C>T (p.Arg925Trp)	rs145933612
NM_004415.4(DSP):c.277T>C (p.Leu93=)	rs1561680562
NM_004415.4(DSP):c.2986-6T>A	rs144748036
NM_004415.4(DSP):c.3018A>G (p.Leu1006=)	rs375412541
NM_004415.4(DSP):c.3102C>T (p.Ile1034=)	rs569974617
NM_004415.4(DSP):c.3123C>T (p.Leu1041=)	rs149929637
NM_004415.4(DSP):c.3303C>T (p.Tyr1101=)	rs372440854
NM_004415.4(DSP):c.3507C>T (p.Tyr1169=)	rs148894066
NM_004415.4(DSP):c.3650C>T (p.Thr1217Met)	rs535202724
NM_004415.4(DSP):c.3701A>G (p.Asn1234Ser)	rs185367490
NM_004415.4(DSP):c.3819C>T (p.Asn1273=)	rs1390665527
NM_004415.4(DSP):c.4032T>C (p.Tyr1344=)	rs1422876320
NM_004415.4(DSP):c.4041A>G (p.Glu1347=)	rs200671552
NM_004415.4(DSP):c.4065T>C (p.Tyr1355=)	rs148478829
NM_004415.4(DSP):c.4320G>A (p.Val1440=)	rs571103583
NM_004415.4(DSP):c.4350G>A (p.Glu1450=)	rs1561698730
NM_004415.4(DSP):c.4372C>G (p.Arg1458Gly)	rs28763965
NM_004415.4(DSP):c.4401A>G (p.Gln1467=)	rs199818953
NM_004415.4(DSP):c.4515G>A (p.Ala1505=)	rs193197554
NM_004415.4(DSP):c.4741A>G (p.Lys1581Glu)	rs186842903
NM_004415.4(DSP):c.4750G>A (p.Ala1584Thr)	rs191778417
NM_004415.4(DSP):c.4752G>A (p.Ala1584=)	rs201213622
NM_004415.4(DSP):c.4943A>G (p.Gln1648Arg)	rs202232360
NM_004415.4(DSP):c.5154G>A (p.Leu1718=)	rs376620183
NM_004415.4(DSP):c.5178C>A (p.Asn1726Lys)	rs147415451
NM_004415.4(DSP):c.5205G>A (p.Arg1735=)	rs1561700008
NM_004415.4(DSP):c.5218G>A (p.Glu1740Lys)	rs142885240
NM_004415.4(DSP):c.5283C>T (p.Asn1761=)	rs763355815
NM_004415.4(DSP):c.5380-15C>A	rs753028657
NM_004415.4(DSP):c.5523A>C (p.Ser1841=)	rs730882116
NM_004415.4(DSP):c.5554C>T (p.Arg1852Cys)	rs550818559
NM_004415.4(DSP):c.5555G>A (p.Arg1852His)	rs193922669
NM_004415.4(DSP):c.5593A>T (p.Asn1865Tyr)	rs562015789
NM_004415.4(DSP):c.5913G>T (p.Leu1971=)	rs373416071
NM_004415.4(DSP):c.6208G>A (p.Asp2070Asn)	rs41302885
NM_004415.4(DSP):c.6373C>T (p.Leu2125=)	rs1246415961
NM_004415.4(DSP):c.6549C>T (p.Tyr2183=)	rs771461040
NM_004415.4(DSP):c.6655G>A (p.Val2219Ile)	rs397516953
NM_004415.4(DSP):c.6678T>A (p.Gly2226=)	rs149070106
NM_004415.4(DSP):c.6804A>G (p.Thr2268=)	rs1561703011
NM_004415.4(DSP):c.6881C>G (p.Ala2294Gly)	rs147000526
NM_004415.4(DSP):c.6918C>T (p.Ser2306=)	rs1275471884
NM_004415.4(DSP):c.6927G>A (p.Arg2309=)	rs747248981
NM_004415.4(DSP):c.7077C>T (p.Ile2359=)	rs966841386
NM_004415.4(DSP):c.7125G>A (p.Gly2375=)	rs141709096
NM_004415.4(DSP):c.7197G>A (p.Glu2399=)	rs372594837
NM_004415.4(DSP):c.729C>T (p.Arg243=)	rs141028505
NM_004415.4(DSP):c.7563T>C (p.Asp2521=)	rs984412074
NM_004415.4(DSP):c.778-6G>T	rs1561685227
NM_004415.4(DSP):c.7854C>G (p.Pro2618=)	rs759590338
NM_004415.4(DSP):c.7983C>A (p.Ile2661=)	rs1561704694
NM_004415.4(DSP):c.8019C>T (p.Asp2673=)	rs144275591
NM_004415.4(DSP):c.8300C>T (p.Thr2767Ile)	rs34884895
NM_004415.4(DSP):c.8415C>T (p.Ala2805=)	rs377148997
NM_004415.4(DSP):c.8529_8540del (p.2827_2830SGSR[4])	rs794728151
NM_004415.4(DSP):c.88G>A (p.Val30Met)	rs121912998

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