List of variants in gene FAM161A, LOC129933843 studied for Retinitis pigmentosa 28

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001201543.2(FAM161A):c.165T>G (p.Ala55=)	rs4270331	0.98177
NM_001201543.2(FAM161A):c.86A>G (p.Gln29Arg)	rs763794474	0.00007
NM_001201543.2(FAM161A):c.122C>T (p.Ala41Val)	rs768878474	0.00002
NM_001201543.2(FAM161A):c.171C>T (p.Pro57=)	rs764002326	0.00001
NM_001201543.2(FAM161A):c.182C>T (p.Ser61Leu)	rs374779101	0.00001
NM_001201543.2(FAM161A):c.105del (p.Pro35_Leu36insTer)
NM_001201543.2(FAM161A):c.110_116dup (p.Ala40fs)
NM_001201543.2(FAM161A):c.125_128delinsGGG (p.Ala42fs)
NM_001201543.2(FAM161A):c.142del (p.Asp48fs)
NM_001201543.2(FAM161A):c.148GAG[2] (p.Glu52del)	rs528451151
NM_001201543.2(FAM161A):c.149A>G (p.Glu50Gly)	rs1673585446
NM_001201543.2(FAM161A):c.64del (p.Ile22fs)
NM_001201543.2(FAM161A):c.70G>T (p.Gly24Ter)	rs2105111295
NM_001201543.2(FAM161A):c.82G>A (p.Ala28Thr)	rs550422472
NM_001201543.2(FAM161A):c.90C>G (p.Tyr30Ter)

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