Related gene-specific medical variations for Gene (Select 51374) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3332398	NM_001170795.4(ATRAID):c.-161A>G	ATRAID, SLC5A6	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3132108	NM_001170795.4(ATRAID):c.-123A>C	LOC129933365, SLC5A6 +1 more	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3132107	NM_001170795.4(ATRAID):c.25C>T (p.Leu9Phe)	ATRAID, LOC129933365 +1 more (L9F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481274	NM_001170795.4(ATRAID):c.13G>T (p.Asp5Tyr)	ATRAID, LOC129933365 +1 more (D5Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471955	NM_001170795.4(ATRAID):c.97G>A (p.Glu33Lys)	ATRAID, SLC5A6 (E33K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471799	NM_001170795.4(ATRAID):c.-74G>C	ATRAID, LOC129933365 +1 more	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2463462	NM_001170795.4(ATRAID):c.-24A>T	ATRAID, LOC129933365 +1 more	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2379207	NM_001170795.4(ATRAID):c.-38C>T	ATRAID, LOC129933365 +1 more	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2313791	NM_001170795.4(ATRAID):c.-71G>A	ATRAID, LOC129933365 +1 more	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2292864	NM_001170795.4(ATRAID):c.-44C>G	ATRAID, LOC129933365 +1 more	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2282359	NM_001170795.4(ATRAID):c.79A>G (p.Arg27Gly)	ATRAID, LOC129933365 +1 more (R27G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance