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NR_136705.1 - -
NR_136704.1 - -
NM_001324105.1 - NP_001311034.1
NM_001324104.1 - NP_001311033.1
NM_007250.5 - NP_009181.2 (MANE)
NM_001324102.1 - NP_001311031.1
NM_001159296.2 - NP_001152768.1
NM_001324100.1 - NP_001311029.1
NM_001324099.1 - NP_001311028.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
X
Location
ChrX:55,907,623-56,292,031
LOEUF
1.313
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ClinVar
Pathogenic/ Likely pa...
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VUS
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GnomAD
Common [>1%]
Rare [<1%]
ToMMo
Common [>1%]
Rare [<1%]
By consequences
Missense
Loss-of-function
Synonymous
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Gene region:
CDS
SpliceSite
UTR
Intron
Flanking
External resources
KLF8
KLF transcription factor 8
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Variant Map
DNA Sequence
Variant Map
Amino Acid Sequence
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