HNRNPM R336P

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Mutation:

Summary

Isoform:

NM_001297418

Position:

336

Ref:

Mutation:

PTM impact:

distal

PTM affected:

Kinases:

Clinical Information

Cancer types: (TCGA MC3)

LUSC

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: 332S

Affected site:

Position: 332

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
329N	LGLD[H/N]HMASSIERMGQ	3	distal
336P	LGLDHMASSIE[R/P]RMGQ	4	distal
337I	LGLDHMASSIER[M/I]MGQ	5	distal

PTM Site: 333S

Affected site:

Position: 333

Residue: S

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
329N	GLD[H/N]HMASSIERMGQT	4	distal
336P	GLDHMASSIE[R/P]RMGQT	3	distal
337I	GLDHMASSIER[M/I]MGQT	4	distal

PTM Site: 340T

Affected site:

Position: 340

Residue: T

Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation	In sequence	Distance	Impact
344V	SIERMGQTMER[I/V]IGSG	4	distal
336P	SIE[R/P]RMGQTMERIGSG	4	distal
337I	SIER[M/I]MGQTMERIGSG	3	distal

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