Related gene-specific medical variations for Gene (Select 64949) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3296101	NM_030811.4(MRPS26):c.67C>T (p.Pro23Ser)	LOC130065317, MRPS26 (P23S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296100	NM_030811.4(MRPS26):c.191G>A (p.Arg64His)	LOC130065317, MRPS26 (R64H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209143	NM_030811.4(MRPS26):c.182A>G (p.Gln61Arg)	LOC130065317, MRPS26 (Q61R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3209142	NM_030811.4(MRPS26):c.132G>A (p.Met44Ile)	LOC130065317, MRPS26 (M44I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460249	NM_030811.4(MRPS26):c.50G>A (p.Arg17Gln)	LOC130065317, MRPS26 (R17Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400804	NM_030811.4(MRPS26):c.124G>A (p.Val42Met)	LOC130065317, MRPS26 (V42M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394082	NM_030811.4(MRPS26):c.7C>G (p.Arg3Gly)	LOC130065317, MRPS26 (R3G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310550	NM_030811.4(MRPS26):c.118G>A (p.Glu40Lys)	LOC130065317, MRPS26 (E40K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260722	NM_030811.4(MRPS26):c.351C>G (p.His117Gln)	LOC130065317, MRPS26 (H117Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248830	NM_030811.4(MRPS26):c.46C>T (p.Pro16Ser)	LOC130065317, MRPS26 (P16S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2239183	NM_030811.4(MRPS26):c.124G>C (p.Val42Leu)	LOC130065317, MRPS26 (V42L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235879	NM_030811.4(MRPS26):c.34A>C (p.Thr12Pro)	LOC130065317, MRPS26 (T12P)	Single nucleotide variant (missense variant)	not specified	GLikely benign