Related gene-specific medical variations for Gene (Select 4216) - ClinVar - NCBI

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Links from Gene

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3122972	NM_005922.4(MAP3K4):c.94C>T (p.Pro32Ser)	MAP3K4, MAP3K4-AS1 (P32S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3122969	NM_005922.4(MAP3K4):c.79C>T (p.Pro27Ser)	MAP3K4, MAP3K4-AS1 (P27S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3122961	NM_005922.4(MAP3K4):c.31C>T (p.Pro11Ser)	MAP3K4, MAP3K4-AS1 (P11S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2525626	NM_005922.4(MAP3K4):c.115G>A (p.Glu39Lys)	MAP3K4, MAP3K4-AS1 (E39K)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2512421	NM_005922.4(MAP3K4):c.139T>G (p.Cys47Gly)	MAP3K4, MAP3K4-AS1 (C47G)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2393218	NM_005922.4(MAP3K4):c.101C>T (p.Pro34Leu)	MAP3K4, MAP3K4-AS1 (P34L)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2358615	NM_005922.4(MAP3K4):c.139T>C (p.Cys47Arg)	MAP3K4, MAP3K4-AS1 (C47R)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2336221	NM_005922.4(MAP3K4):c.137G>T (p.Cys46Phe)	MAP3K4, MAP3K4-AS1 (C46F)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 221815	GRCh37/hg19 6q26(chr6:161362678-161469774)x3	MAP3K4	Copy number gain	Premature ovarian failure	GBenign