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Variants
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5
records found for search term
Tmem191c
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RGD ID
Symbol
Variant Type
Name
Trait
Clinical Significance
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Annotations
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156240310
CV2245967
single nucleotide variant
NM_001388354.1(
TMEM191C
):c.-24C>T
not specified [RCV004113896]
uncertain significance
22
21467436
21467436
Human
name
156279839
CV2338345
single nucleotide variant
NM_001388354.1(
TMEM191C
):c.525+5G>A
not specified [RCV004186396]
uncertain significance
22
21469008
21469008
Human
name
155959161
CV2193759
single nucleotide variant
NM_001388354.1(
TMEM191C
):c.2T>C (p.Met1Thr)
not specified [RCV004074521]
uncertain significance
22
21467461
21467461
Human
name
155971507
CV2334224
single nucleotide variant
NM_001388354.1(
TMEM191C
):c.62G>A (p.Arg21Gln)
not specified [RCV004186208]
uncertain significance
22
21467521
21467521
Human
name
155920341
CV2240347
single nucleotide variant
NM_001388354.1(
TMEM191C
):c.656C>A (p.Ala219Glu)
not specified [RCV004117252]
uncertain significance
22
21469339
21469339
Human
name