List of variants in gene MTPAP reported as benign for not provided

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

Total variants: 45

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HGVS	dbSNP	gnomAD frequency
NM_018109.4(MTPAP):c.993-68G>A	rs2484284	0.99932
NC_000010.11:g.30349429G>A	rs2782976	0.99473
NM_018109.4(MTPAP):c.331-170C>A	rs2252246	0.95502
NM_018109.4(MTPAP):c.555+73G>A	rs2689215	0.95479
NM_018109.4(MTPAP):c.781-74T>C	rs1029172	0.95370
NM_018109.4(MTPAP):c.992+163G>A	rs2484286	0.93713
NM_018109.4(MTPAP):c.1220-271C>T	rs2990499	0.69431
NM_018109.3(MTPAP):c.-311G>A	rs3824709	0.40221
NM_018109.4(MTPAP):c.157+53G>C	rs10826783	0.40140
NM_018109.4(MTPAP):c.556-47G>A	rs12221163	0.40088
NM_018109.4(MTPAP):c.555+19C>T	rs1047988	0.25271
NM_018109.4(MTPAP):c.484C>T (p.Arg162Cys)	rs1047991	0.24628
NM_018109.4(MTPAP):c.993-228A>C	rs2480295	0.21447
NM_018109.3(MTPAP):c.-393G>T	rs2689212	0.21041
NM_018109.4(MTPAP):c.556-266C>T	rs11007998	0.11640
NM_018109.4(MTPAP):c.780+211A>G	rs913644	0.11208
NM_018109.4(MTPAP):c.1219+37C>G	rs7085884	0.08998
NM_018109.3(MTPAP):c.-104C>T	rs11815219	0.07429
NM_018109.4(MTPAP):c.1386+107T>C	rs77572290	0.05846
NM_018109.4(MTPAP):c.555+118C>G	rs74443112	0.05495
NM_018109.4(MTPAP):c.993-295C>T	rs111939752	0.05343
NM_018109.4(MTPAP):c.330+251C>T	rs7893864	0.02912
NM_018109.4(MTPAP):c.158-27G>A	rs73236442	0.01828
NM_018109.4(MTPAP):c.158-9C>T	rs139217290	0.00503
NM_018109.4(MTPAP):c.585G>A (p.Lys195=)	rs144945655	0.00240
NM_018109.4(MTPAP):c.1637G>A (p.Ser546Asn)	rs17855116	0.00217
NM_018109.4(MTPAP):c.1485G>A (p.Leu495=)	rs142672993	0.00143
NM_018109.4(MTPAP):c.1312+3A>G	rs117698926	0.00031
NM_018109.4(MTPAP):c.138T>C (p.Pro46=)	rs147352132	0.00031
NM_018109.4(MTPAP):c.916T>C (p.Leu306=)	rs191209359	0.00013
NM_018109.4(MTPAP):c.992+8C>T	rs747331939	0.00007
NM_018109.4(MTPAP):c.345C>T (p.Val115=)	rs548128535	0.00006
NM_018109.4(MTPAP):c.556-11C>T	rs188101690	0.00004
NM_018109.4(MTPAP):c.486C>T (p.Arg162=)	rs150489876	0.00003
NM_018109.4(MTPAP):c.1036C>T (p.Leu346=)	rs775249623	0.00001
NC_000010.11:g.30349357A>G	rs10826784
NC_000010.11:g.30349359_30349360insAG	rs1554819278
NC_000010.11:g.30349360_30349361insAG	rs150495221
NC_000010.11:g.30349366del	rs71525586
NM_018109.4(MTPAP):c.1386+114del	rs142868943
NM_018109.4(MTPAP):c.1473T>C (p.Ser491=)
NM_018109.4(MTPAP):c.331-19dup
NM_018109.4(MTPAP):c.331-60_331-56del	rs36002941
NM_018109.4(MTPAP):c.556-198C>T	rs112319038
NM_018109.4(MTPAP):c.780+266A>G	rs73236434

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