STARD13 V38M

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Mutation:

Summary

Isoform:

NM_001243474

Position:

Ref:

Mutation:

PTM impact:

proximal

PTM affected:

Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

[0.1615]

Minor Allele Frequency: (1000 Genomes)

[0.0199681]

PTM Site: 36S

Affected site:

Position: 36

Residue: S

Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
40N	QRTSRRWSRVD[D/N]DLYT	4	distal
38M	QRTSRRWSR[V/M]VDDLYT	2	proximal
33H	QRTS[R/H]RRWSRVDDLYT	3	network-rewiring
31S	QR[T/S]TSRRWSRVDDLYT	5	distal
37L	QRTSRRWS[R/L]RVDDLYT	1	proximal

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

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