STARD13 R47Q

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Mutation:

Summary

Isoform:

NM_001243474

Position:

Ref:

Mutation:

PTM impact:

distal

PTM affected:

Kinases:

Clinical Information

Cancer types: (TCGA MC3)

BLCA

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 42Y

Affected site:

Position: 42

Residue: Y

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
40N	WSRVD[D/N]DLYTLLPRGD	2	proximal
38M	WSR[V/M]VDDLYTLLPRGD	4	distal
37L	WS[R/L]RVDDLYTLLPRGD	5	distal
44M	WSRVDDLYT[L/M]LLPRGD	2	proximal
47Q	WSRVDDLYTLLP[R/Q]RGD	5	distal

PTM Site: 43T

Affected site:

Position: 43

Residue: T

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
40N	SRVD[D/N]DLYTLLPRGDR	3	distal
38M	SR[V/M]VDDLYTLLPRGDR	5	distal
37L	S[R/L]RVDDLYTLLPRGDR	6	distal
44M	SRVDDLYT[L/M]LLPRGDR	1	proximal
47Q	SRVDDLYTLLP[R/Q]RGDR	4	distal

PTM Site: 53S

Affected site:

Position: 53

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
57M	PRGDRNGSPGG[T/M]TGMR	4	distal
51S	PRGDR[N/S]NGSPGGTGMR	2	proximal
54L	PRGDRNGS[P/L]PGGTGMR	1	network-rewiring
53L	PRGDRNG[S/L]SPGGTGMR	0	direct
52V	PRGDRN[G/V]GSPGGTGMR	1	proximal
47Q	P[R/Q]RGDRNGSPGGTGMR	6	distal

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