Related gene-specific medical variations for Gene (Select 2252) - ClinVar - NCBI

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

Display options Sort by Relevance Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File

Links from Gene

Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3094755	NM_002009.4(FGF7):c.80C>G (p.Thr27Ser)	FAM227B, FGF7 (T27S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094754	NM_002009.4(FGF7):c.539A>C (p.Lys180Thr)	FAM227B, FGF7 (K180T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094753	NM_002009.4(FGF7):c.107C>T (p.Thr36Ile)	FAM227B, FGF7 (T36I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480711	NM_002009.4(FGF7):c.76G>T (p.Gly26Cys)	FAM227B, FGF7 (G26C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

Display options Sort by Relevance Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File