"MLF1-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File

Search results

Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058750	NM_001369783.1(MLF1):c.201G>T (p.Thr67=)	MLF1	Single nucleotide variant (synonymous variant +1 more)	MLF1-related condition	GLikely benign
Select item 778840	NM_001369783.1(MLF1):c.600C>T (p.Ile200=)	MLF1	Single nucleotide variant (synonymous variant)	MLF1-related condition +1 more	GBenign
Select item 3058810	NM_001369783.1(MLF1):c.614-3T>C	MLF1	Single nucleotide variant (intron variant)	MLF1-related condition	GLikely benign
Select item 3059532	NM_001369783.1(MLF1):c.615T>C (p.Ser205=)	MLF1	Single nucleotide variant (synonymous variant +1 more)	MLF1-related condition	GBenign
Select item 3060448	NM_001369783.1(MLF1):c.721C>A (p.Pro241Thr)	MLF1 (P152T +7 more)	Single nucleotide variant (missense variant +1 more)	MLF1-related condition	GBenign

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File